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Peter Marhavý at the confocal microscope

Marhavý, Peter - Short distance communication in response to wound stress

Research

Peter Marhavy at the confocal microscopePhoto: Fredrik Larsson

In my group, we are studying the mechanisms involved in short distance cell-to-cell communication in response to localized wound stress in plant roots using plant parasitic nematodes and state-of-the-art laser ablation approach.

Plants are able to recognize biotic, abiotic and physical stressors and orchestrate different signaling pathways accordingly. Although defensive stress response signals have been intensively studied and documented, the exact mechanisms by which these signals are perceived by cells and how the signal is further transmitted from one cell to another are still largely unknown. Our research will provide insights into molecular mechanisms of cell-to-cell communication to underlying early responses to wounding in plant roots.

  
Real-time monitoring of calcium wave propagation after cortex cell ablation using an R-GECO1 reporter line. Laser ablation of cortex cells leads to signal increases a few seconds after ablation at the ablated root side (indicated by white arrow). In non-ablated control roots, no changes of signal intensity were observed.
Arabidopsis root expressing SCR::SCR-YFP (green) in endodermis and stained with cell-wall fluorescence dye propidium iodide (red). Time lapse demonstrate single cell laser ablation in root meristem. White arrow indicates ablated cell.
Real-time monitoring (xyt) of cyst nematodes (Heterodera schachtii) during infection in 5-day-old roots of Arabidopsis thaliana stained with propidium iodide (red). Video demonstrate nematode progression between epidermal cells.

Group Members

  • Personnel Image
    Di Fino, Luciano Martìn
    PostDoc
    E-mail
    Room: B5-48-45
  • Personnel Image
    Ducla, Julie
    PhD Student
    E-mail
    Room: B5-48-45
  • Personnel Image
    Ingremeau, Mathis
    Project Student
    E-mail
    Room: KB5C8
  • Personnel Image
    Mentzelopoulou, Andriani
    PostDoc
    E-mail
    Room: B5-16-45

CV P. Marhavý

  • 2020 - to date: Researcher, Swedish University of Agricultural Sciences, Umeå, Sweden
  • 2015 – 2019: Post-doctoral researcher, University of Lausanne Department of Plant Molecular Biology, Lausanne, Switzerland
  • 2013 – 2014: Post-doctoral researcher, The Institute of Science and Technology Austria, Klosterneuburg, Austria
  • 2012 – 2013: Post-doctoral researcher, VIB Department of Plant Systems Biology, Ghent, Belgium
  • 2012: Doctor of Science - Biochemistry and Biotechnology, VIB Department of Plant Systems Biology, Ghent University, Belgium
  • 2008: Master of Science - Molecular Biology, Comenius University, Faculty of Natural Science, Bratislava Slovakia
  • 2006: Bachelor of Science – Biology, Comenius University, Faculty of Natural Science, Bratislava Slovakia

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  2025 (4)
Ca2+ waves and ethylene/JA crosstalk orchestrate wound responses in Arabidopsis roots. Ma, X., Hasan, M S., Anjam, M. S., Mahmud, S., Bhattacharyya, S., Vothknecht, U. C, Mendy, B., Grundler, F. M W, & Marhavý, P. EMBO reports, 26(12): 3187–3203. June 2025. Num Pages: 3203 Publisher: John Wiley & Sons, Ltd
Ca2+ waves and ethylene/JA crosstalk orchestrate wound responses in Arabidopsis roots [link]Paper   doi   link   bibtex   abstract  
@article{ma_ca2_2025,
	title = {Ca2+ waves and ethylene/{JA} crosstalk orchestrate wound responses in {Arabidopsis} roots},
	volume = {26},
	issn = {1469-221X},
	url = {https://www.embopress.org/doi/full/10.1038/s44319-025-00471-z},
	doi = {10.1038/s44319-025-00471-z},
	abstract = {Wounding triggers complex and multi-faceted responses in plants. Among these, calcium (Ca2+) waves serve as an immediate and localized response to strong stimuli, such as nematode infection or laser ablation. Here, we investigate the propagation patterns of Ca2+ waves induced by laser ablation and observe that glutamate-receptor-like channels (GLR3.3/GLR3.6), the stretch-activated anion channel MSL10, and the mechanosensitive Ca2+-permeable channels MCA1/MCA2 influence this process. These channels contribute to ethylene-associated signaling pathways, potentially through the WRKY33-ACS6 regulatory network. Furthermore, our findings show that ACC/ethylene signaling modulates Ca2+ wave propagation following laser ablation. Ethylene perception and synthesis at the site of damage regulate the local jasmonate response, which displays tissue-specific patterns upon laser ablation. Overall, our data provide new insights into the molecular and cellular processes underlying plant responses to localized damage, highlighting the roles of specific ion channels and hormone signaling pathways in shaping these responses in Arabidopsis roots.},
	number = {12},
	urldate = {2025-06-27},
	journal = {EMBO reports},
	author = {Ma, Xuemin and Hasan, M Shamim and Anjam, Muhammad Shahzad and Mahmud, Sakil and Bhattacharyya, Sabarna and Vothknecht, Ute C and Mendy, Badou and Grundler, Florian M W and Marhavý, Peter},
	month = jun,
	year = {2025},
	note = {Num Pages: 3203
Publisher: John Wiley \& Sons, Ltd},
	keywords = {Ca2+ Wave, Ethylene, Jasmonate, Laser Ablation},
	pages = {3187--3203},
}







Wounding triggers complex and multi-faceted responses in plants. Among these, calcium (Ca2+) waves serve as an immediate and localized response to strong stimuli, such as nematode infection or laser ablation. Here, we investigate the propagation patterns of Ca2+ waves induced by laser ablation and observe that glutamate-receptor-like channels (GLR3.3/GLR3.6), the stretch-activated anion channel MSL10, and the mechanosensitive Ca2+-permeable channels MCA1/MCA2 influence this process. These channels contribute to ethylene-associated signaling pathways, potentially through the WRKY33-ACS6 regulatory network. Furthermore, our findings show that ACC/ethylene signaling modulates Ca2+ wave propagation following laser ablation. Ethylene perception and synthesis at the site of damage regulate the local jasmonate response, which displays tissue-specific patterns upon laser ablation. Overall, our data provide new insights into the molecular and cellular processes underlying plant responses to localized damage, highlighting the roles of specific ion channels and hormone signaling pathways in shaping these responses in Arabidopsis roots.
Cellular damage triggers mechano-chemical control of cell wall dynamics and patterned cell divisions in plant healing. Di Fino, L. M., Anjam, M. S., Besten, M., Mentzelopoulou, A., Papadakis, V., Zahid, N., Baez, L. A., Trozzi, N., Majda, M., Ma, X., Hamann, T., Sprakel, J., Moschou, P. N., Smith, R. S., & Marhavý, P. Developmental Cell, 60(10): 1411–1422.e6. May 2025.
Cellular damage triggers mechano-chemical control of cell wall dynamics and patterned cell divisions in plant healing [link]Paper   doi   link   bibtex   abstract  
@article{di_fino_cellular_2025,
	title = {Cellular damage triggers mechano-chemical control of cell wall dynamics and patterned cell divisions in plant healing},
	volume = {60},
	issn = {1534-5807},
	url = {https://www.sciencedirect.com/science/article/pii/S1534580724007718},
	doi = {10.1016/j.devcel.2024.12.032},
	abstract = {Reactivation of cell division is crucial for the regeneration of damaged tissues, which is a fundamental process across all multicellular organisms. However, the mechanisms underlying the activation of cell division in plants during regeneration remain poorly understood. Here, we show that single-cell endodermal ablation generates a transient change in the local mechanical pressure on neighboring pericycle cells to activate patterned cell division that is crucial for tissue regeneration in Arabidopsis roots. Moreover, we provide strong evidence that this process relies on the phytohormone ethylene. Thus, our results highlight a previously unrecognized role of mechano-chemical control in patterned cell division during regeneration in plants.},
	number = {10},
	urldate = {2025-05-23},
	journal = {Developmental Cell},
	author = {Di Fino, Luciano Martín and Anjam, Muhammad Shahzad and Besten, Maarten and Mentzelopoulou, Andriani and Papadakis, Vassilis and Zahid, Nageena and Baez, Luis Alonso and Trozzi, Nicola and Majda, Mateusz and Ma, Xuemin and Hamann, Thorsten and Sprakel, Joris and Moschou, Panagiotis N. and Smith, Richard S. and Marhavý, Peter},
	month = may,
	year = {2025},
	keywords = {cell division, cell wall, ethylene, mechanobiology, pectin, regeneration, single-cell laser ablation, xylem-pole-pericycle},
	pages = {1411--1422.e6},
}















Reactivation of cell division is crucial for the regeneration of damaged tissues, which is a fundamental process across all multicellular organisms. However, the mechanisms underlying the activation of cell division in plants during regeneration remain poorly understood. Here, we show that single-cell endodermal ablation generates a transient change in the local mechanical pressure on neighboring pericycle cells to activate patterned cell division that is crucial for tissue regeneration in Arabidopsis roots. Moreover, we provide strong evidence that this process relies on the phytohormone ethylene. Thus, our results highlight a previously unrecognized role of mechano-chemical control in patterned cell division during regeneration in plants.
Damage activates EXG1 and RLP44 to suppress vascular differentiation during regeneration in Arabidopsis. Mazumdar, S., Augstein, F., Zhang, A., Musseau, C., Anjam, M. S., Marhavy, P., & Melnyk, C. W. Plant Communications, 6(4): 101256. April 2025.
Damage activates <i>EXG1</i> and <i>RLP44</i> to suppress vascular differentiation during regeneration in <i>Arabidopsis</i> [link]Paper   doi   link   bibtex   abstract  
@article{mazumdar_damage_2025,
	title = {Damage activates \textit{{EXG1}} and \textit{{RLP44}} to suppress vascular differentiation during regeneration in \textit{{Arabidopsis}}},
	volume = {6},
	issn = {2590-3462},
	url = {https://www.sciencedirect.com/science/article/pii/S2590346225000185},
	doi = {10.1016/j.xplc.2025.101256},
	abstract = {Plants possess remarkable regenerative abilities to form de novo vasculature after damage and in response to pathogens that invade and withdraw nutrients. To identify common factors that affect vascular formation upon stress, we searched for Arabidopsis thaliana genes differentially expressed upon Agrobacterium infection, nematode infection, and plant grafting. One such gene is cell wall-related and highly induced by all three stresses, which we named ENHANCED XYLEM AND GRAFTING1 (EXG1), since its mutations promote ectopic xylem formation in a vascular cell induction system and enhance graft formation. Further observations revealed that exg1 mutants show inhibited cambium development and callus formation but enhanced tissue attachment, syncytium size, phloem reconnection, and xylem formation. Given that brassinosteroids also promote xylem differentiation, we analyzed brassinosteroid-related genes and found that mutations in RLP44 encoding a receptor-like protein cause similar regeneration-related phenotypes as mutations in EXG1. Like EXG1, RLP44 expression is also induced by grafting and wounding. Mutations in EXG1 and RLP44 affect the expression of many genes in common, including those related to cell walls and genes important for vascular regeneration. Our results suggest that EXG1 integrates information from wounding or pathogen stress and functions with RLP44 to suppress vascular differentiation during regeneration and healing.},
	number = {4},
	urldate = {2025-04-22},
	journal = {Plant Communications},
	author = {Mazumdar, Shamik and Augstein, Frauke and Zhang, Ai and Musseau, Constance and Anjam, Muhammad Shahzad and Marhavy, Peter and Melnyk, Charles W.},
	month = apr,
	year = {2025},
	keywords = {Cell wall, Grafting, Regeneration, Stress, Wounding, Xylem, cell wall, grafting, regeneration, stress, wounding, xylem},
	pages = {101256},
}







Plants possess remarkable regenerative abilities to form de novo vasculature after damage and in response to pathogens that invade and withdraw nutrients. To identify common factors that affect vascular formation upon stress, we searched for Arabidopsis thaliana genes differentially expressed upon Agrobacterium infection, nematode infection, and plant grafting. One such gene is cell wall-related and highly induced by all three stresses, which we named ENHANCED XYLEM AND GRAFTING1 (EXG1), since its mutations promote ectopic xylem formation in a vascular cell induction system and enhance graft formation. Further observations revealed that exg1 mutants show inhibited cambium development and callus formation but enhanced tissue attachment, syncytium size, phloem reconnection, and xylem formation. Given that brassinosteroids also promote xylem differentiation, we analyzed brassinosteroid-related genes and found that mutations in RLP44 encoding a receptor-like protein cause similar regeneration-related phenotypes as mutations in EXG1. Like EXG1, RLP44 expression is also induced by grafting and wounding. Mutations in EXG1 and RLP44 affect the expression of many genes in common, including those related to cell walls and genes important for vascular regeneration. Our results suggest that EXG1 integrates information from wounding or pathogen stress and functions with RLP44 to suppress vascular differentiation during regeneration and healing.
TYPHON proteins are RAB-dependent mediators of the trans-Golgi network secretory pathway. Baral, A., Gendre, D., Aryal, B., Fougère, L., Di Fino, L. M., Ohori, C., Sztojka, B., Uemura, T., Ueda, T., Marhavý, P., Boutté, Y., & Bhalerao, R. P The Plant Cell, 37(1): koae280. January 2025.
TYPHON proteins are RAB-dependent mediators of the trans-Golgi network secretory pathway [link]Paper   doi   link   bibtex   abstract  
@article{baral_typhon_2025,
	title = {{TYPHON} proteins are {RAB}-dependent mediators of the trans-{Golgi} network secretory pathway},
	volume = {37},
	issn = {1040-4651},
	url = {https://doi.org/10.1093/plcell/koae280},
	doi = {10.1093/plcell/koae280},
	abstract = {The trans-Golgi network (TGN), a key compartment in endomembrane trafficking, participates in both secretion to and endocytosis from the plasma membrane. Consequently, the TGN plays a key role in plant growth and development. Understanding how proteins are sorted for secretion or endocytic recycling at the TGN is critical for elucidating mechanisms of plant development. We previously showed that the protein ECHIDNA is essential for phytohormonal control of hypocotyl bending because it mediates secretion of cell wall components and the auxin influx carrier AUXIN RESISTANT 1 (AUX1) from the TGN. Despite the critical role of ECHIDNA in TGN-mediated trafficking, its mode of action remains unknown in Arabidopsis (Arabidopsis thaliana). We therefore performed a suppressor screen on the ech mutant. Here, we report the identification of TGN-localized TYPHON 1 (TPN1) and TPN2 proteins. A single amino acid change in either TPN protein causes dominant suppression of the ech mutant's defects in growth and AUX1 secretion, while also restoring wild-type (WT)-like ethylene-responsive hypocotyl bending. Importantly, genetic and cell biological evidence shows that TPN1 acts through RAS-ASSOCIATED BINDING H1b (RABH1b), a TGN-localized RAB-GTPase. These results provide insights into ECHIDNA-mediated secretory trafficking of cell wall and auxin carriers at the TGN, as well as its role in controlling plant growth.},
	number = {1},
	urldate = {2025-01-20},
	journal = {The Plant Cell},
	author = {Baral, Anirban and Gendre, Delphine and Aryal, Bibek and Fougère, Louise and Di Fino, Luciano Martin and Ohori, Chihiro and Sztojka, Bernadette and Uemura, Tomohiro and Ueda, Takashi and Marhavý, Peter and Boutté, Yohann and Bhalerao, Rishikesh P},
	month = jan,
	year = {2025},
	pages = {koae280},
}







The trans-Golgi network (TGN), a key compartment in endomembrane trafficking, participates in both secretion to and endocytosis from the plasma membrane. Consequently, the TGN plays a key role in plant growth and development. Understanding how proteins are sorted for secretion or endocytic recycling at the TGN is critical for elucidating mechanisms of plant development. We previously showed that the protein ECHIDNA is essential for phytohormonal control of hypocotyl bending because it mediates secretion of cell wall components and the auxin influx carrier AUXIN RESISTANT 1 (AUX1) from the TGN. Despite the critical role of ECHIDNA in TGN-mediated trafficking, its mode of action remains unknown in Arabidopsis (Arabidopsis thaliana). We therefore performed a suppressor screen on the ech mutant. Here, we report the identification of TGN-localized TYPHON 1 (TPN1) and TPN2 proteins. A single amino acid change in either TPN protein causes dominant suppression of the ech mutant's defects in growth and AUX1 secretion, while also restoring wild-type (WT)-like ethylene-responsive hypocotyl bending. Importantly, genetic and cell biological evidence shows that TPN1 acts through RAS-ASSOCIATED BINDING H1b (RABH1b), a TGN-localized RAB-GTPase. These results provide insights into ECHIDNA-mediated secretory trafficking of cell wall and auxin carriers at the TGN, as well as its role in controlling plant growth.
  2024 (2)
A proxitome-RNA-capture approach reveals that processing bodies repress coregulated hub genes. Liu, C., Mentzelopoulou, A., Hatzianestis, I. H, Tzagkarakis, E., Skaltsogiannis, V., Ma, X., Michalopoulou, V. A, Romero-Campero, F. J, Romero-Losada, A. B, Sarris, P. F, Marhavy, P., Bölter, B., Kanterakis, A., Gutierrez-Beltran, E., & Moschou, P. N The Plant Cell, 36(3): 559–584. March 2024.
A proxitome-RNA-capture approach reveals that processing bodies repress coregulated hub genes [link]Paper   doi   link   bibtex   abstract  
@article{liu_proxitome-rna-capture_2024,
	title = {A proxitome-{RNA}-capture approach reveals that processing bodies repress coregulated hub genes},
	volume = {36},
	issn = {1040-4651},
	url = {https://doi.org/10.1093/plcell/koad288},
	doi = {10.1093/plcell/koad288},
	abstract = {Cellular condensates are usually ribonucleoprotein assemblies with liquid- or solid-like properties. Because these subcellular structures lack a delineating membrane, determining their compositions is difficult. Here we describe a proximity-biotinylation approach for capturing the RNAs of the condensates known as processing bodies (PBs) in Arabidopsis (Arabidopsis thaliana). By combining this approach with RNA detection, in silico, and high-resolution imaging approaches, we studied PBs under normal conditions and heat stress. PBs showed a much more dynamic RNA composition than the total transcriptome. RNAs involved in cell wall development and regeneration, plant hormonal signaling, secondary metabolism/defense, and RNA metabolism were enriched in PBs. RNA-binding proteins and the liquidity of PBs modulated RNA recruitment, while RNAs were frequently recruited together with their encoded proteins. In PBs, RNAs follow distinct fates: in small liquid-like PBs, RNAs get degraded while in more solid-like larger ones, they are stored. PB properties can be regulated by the actin-polymerizing SCAR (suppressor of the cyclic AMP)-WAVE (WASP family verprolin homologous) complex. SCAR/WAVE modulates the shuttling of RNAs between PBs and the translational machinery, thereby adjusting ethylene signaling. In summary, we provide an approach to identify RNAs in condensates that allowed us to reveal a mechanism for regulating RNA fate.},
	number = {3},
	urldate = {2024-03-01},
	journal = {The Plant Cell},
	author = {Liu, Chen and Mentzelopoulou, Andriani and Hatzianestis, Ioannis H and Tzagkarakis, Epameinondas and Skaltsogiannis, Vasileios and Ma, Xuemin and Michalopoulou, Vassiliki A and Romero-Campero, Francisco J and Romero-Losada, Ana B and Sarris, Panagiotis F and Marhavy, Peter and Bölter, Bettina and Kanterakis, Alexandros and Gutierrez-Beltran, Emilio and Moschou, Panagiotis N},
	month = mar,
	year = {2024},
	pages = {559--584},
}



Cellular condensates are usually ribonucleoprotein assemblies with liquid- or solid-like properties. Because these subcellular structures lack a delineating membrane, determining their compositions is difficult. Here we describe a proximity-biotinylation approach for capturing the RNAs of the condensates known as processing bodies (PBs) in Arabidopsis (Arabidopsis thaliana). By combining this approach with RNA detection, in silico, and high-resolution imaging approaches, we studied PBs under normal conditions and heat stress. PBs showed a much more dynamic RNA composition than the total transcriptome. RNAs involved in cell wall development and regeneration, plant hormonal signaling, secondary metabolism/defense, and RNA metabolism were enriched in PBs. RNA-binding proteins and the liquidity of PBs modulated RNA recruitment, while RNAs were frequently recruited together with their encoded proteins. In PBs, RNAs follow distinct fates: in small liquid-like PBs, RNAs get degraded while in more solid-like larger ones, they are stored. PB properties can be regulated by the actin-polymerizing SCAR (suppressor of the cyclic AMP)-WAVE (WASP family verprolin homologous) complex. SCAR/WAVE modulates the shuttling of RNAs between PBs and the translational machinery, thereby adjusting ethylene signaling. In summary, we provide an approach to identify RNAs in condensates that allowed us to reveal a mechanism for regulating RNA fate.
Redox signalling in plant–nematode interactions: Insights into molecular crosstalk and defense mechanisms. Hasan, M. S., Lin, C., Marhavy, P., Kyndt, T., & Siddique, S. Plant, Cell & Environment, 47(8): 2811–2820. 2024. _eprint: https://onlinelibrary.wiley.com/doi/pdf/10.1111/pce.14925
Redox signalling in plant–nematode interactions: Insights into molecular crosstalk and defense mechanisms [link]Paper   doi   link   bibtex   abstract  
@article{hasan_redox_2024,
	title = {Redox signalling in plant–nematode interactions: {Insights} into molecular crosstalk and defense mechanisms},
	volume = {47},
	copyright = {© 2024 John Wiley \& Sons Ltd.},
	issn = {1365-3040},
	shorttitle = {Redox signalling in plant–nematode interactions},
	url = {https://onlinelibrary.wiley.com/doi/abs/10.1111/pce.14925},
	doi = {10.1111/pce.14925},
	abstract = {Plant–parasitic nematodes, specifically cyst nematodes (CNs) and root-knot nematodes (RKNs), pose significant threats to global agriculture, leading to substantial crop losses. Both CNs and RKNs induce permanent feeding sites in the root of their host plants, which then serve as their only source of nutrients throughout their lifecycle. Plants deploy reactive oxygen species (ROS) as a primary defense mechanism against nematode invasion. Notably, both CNs and RKNs have evolved sophisticated strategies to manipulate the host's redox environment to their advantage, with each employing distinct tactics to combat ROS. In this review, we have focused on the role of ROS and its scavenging network in interactions between host plants and CNs and RKNs. Overall, this review emphasizes the complex interplay between plant defense mechanism, redox signalling and nematode survival tactics, suggesting potential avenues for developing innovative nematode management strategies in agriculture.},
	language = {en},
	number = {8},
	urldate = {2024-07-19},
	journal = {Plant, Cell \& Environment},
	author = {Hasan, M. Shamim and Lin, Ching-Jung and Marhavy, Peter and Kyndt, Tina and Siddique, Shahid},
	year = {2024},
	note = {\_eprint: https://onlinelibrary.wiley.com/doi/pdf/10.1111/pce.14925},
	keywords = {ROS, antioxidants, cyst nematodes, effectors, root-knot nematodes},
	pages = {2811--2820},
}



Plant–parasitic nematodes, specifically cyst nematodes (CNs) and root-knot nematodes (RKNs), pose significant threats to global agriculture, leading to substantial crop losses. Both CNs and RKNs induce permanent feeding sites in the root of their host plants, which then serve as their only source of nutrients throughout their lifecycle. Plants deploy reactive oxygen species (ROS) as a primary defense mechanism against nematode invasion. Notably, both CNs and RKNs have evolved sophisticated strategies to manipulate the host's redox environment to their advantage, with each employing distinct tactics to combat ROS. In this review, we have focused on the role of ROS and its scavenging network in interactions between host plants and CNs and RKNs. Overall, this review emphasizes the complex interplay between plant defense mechanism, redox signalling and nematode survival tactics, suggesting potential avenues for developing innovative nematode management strategies in agriculture.
  2023 (1)
Unveiling the intricate mechanisms of plant defense. Guerreiro, J., & Marhavý, P. Frontiers in Plant Physiology, 1. 2023.
Unveiling the intricate mechanisms of plant defense [link]Paper   doi   link   bibtex   abstract  
@article{guerreiro_unveiling_2023,
	title = {Unveiling the intricate mechanisms of plant defense},
	volume = {1},
	issn = {2813-821X},
	url = {https://www.frontiersin.org/articles/10.3389/fphgy.2023.1285373},
	doi = {10.3389/fphgy.2023.1285373},
	abstract = {Plants may lack mobility, but they are not defenseless against the constant threats posed by pathogens and pests. Pattern Recognition Receptors (PRRs), which are located on the plasma membrane, enable plants to effectively recognize intruders. These receptors function by sensing elicitors or fragments of the cell wall that arise from damage. Recent studies underscore the significance of maintaining cell wall integrity in the coordination of defense mechanisms following the detection of parasitism. Pathogen invasion often triggers alterations in cell wall structure, which leads to the release of molecules like β-glucans and oligogalacturonides. These small molecules are then recognized by PRRs, which stimulate downstream signaling pathways that involve both receptor-like kinases and calcium-dependent signaling. Here, we present the latest insights into plant signaling that play a vital role in immunity: the maintenance of cell wall integrity; the intricate interplay between receptor-like kinases; and the involvement of calcium ions. The goal of the review is to provide readers with a deeper understanding of the intricate mechanisms underlying plant defense strategies.},
	urldate = {2024-02-08},
	journal = {Frontiers in Plant Physiology},
	author = {Guerreiro, Julie and Marhavý, Peter},
	year = {2023},
}



Plants may lack mobility, but they are not defenseless against the constant threats posed by pathogens and pests. Pattern Recognition Receptors (PRRs), which are located on the plasma membrane, enable plants to effectively recognize intruders. These receptors function by sensing elicitors or fragments of the cell wall that arise from damage. Recent studies underscore the significance of maintaining cell wall integrity in the coordination of defense mechanisms following the detection of parasitism. Pathogen invasion often triggers alterations in cell wall structure, which leads to the release of molecules like β-glucans and oligogalacturonides. These small molecules are then recognized by PRRs, which stimulate downstream signaling pathways that involve both receptor-like kinases and calcium-dependent signaling. Here, we present the latest insights into plant signaling that play a vital role in immunity: the maintenance of cell wall integrity; the intricate interplay between receptor-like kinases; and the involvement of calcium ions. The goal of the review is to provide readers with a deeper understanding of the intricate mechanisms underlying plant defense strategies.
  2022 (3)
CASP microdomain formation requires cross cell wall stabilization of domains and non-cell autonomous action of LOTR1. Kolbeck, A., Marhavý, P., De Bellis, D., Li, B., Kamiya, T., Fujiwara, T., Kalmbach, L., & Geldner, N. eLife, 11: e69602. January 2022.
CASP microdomain formation requires cross cell wall stabilization of domains and non-cell autonomous action of LOTR1 [link]Paper   doi   link   bibtex   abstract  
@article{kolbeck_casp_2022,
	title = {{CASP} microdomain formation requires cross cell wall stabilization of domains and non-cell autonomous action of {LOTR1}},
	volume = {11},
	issn = {2050-084X},
	url = {https://doi.org/10.7554/eLife.69602},
	doi = {10/gpjfdm},
	abstract = {Efficient uptake of nutrients in both animal and plant cells requires tissue-spanning diffusion barriers separating inner tissues from the outer lumen/soil. However, we poorly understand how such contiguous three-dimensional superstructures are formed in plants. Here, we show that correct establishment of the plant Casparian Strip (CS) network relies on local neighbor communication. We show that positioning of Casparian Strip membrane domains (CSDs) is tightly coordinated between neighbors in wild-type and that restriction of domain formation involves the putative extracellular protease LOTR1. Impaired domain restriction in lotr1 leads to fully functional CSDs at ectopic positions, forming ‘half strips’. LOTR1 action in the endodermis requires its expression in the stele. LOTR1 endodermal expression cannot complement, while cortex expression causes a dominant-negative phenotype. Our findings establish LOTR1 as a crucial player in CSD positioning acting in a directional, non-cell-autonomous manner to restrict and coordinate CS positioning.},
	urldate = {2022-02-17},
	journal = {eLife},
	author = {Kolbeck, Andreas and Marhavý, Peter and De Bellis, Damien and Li, Baohai and Kamiya, Takehiro and Fujiwara, Toru and Kalmbach, Lothar and Geldner, Niko},
	editor = {Benitez-Alfonso, Yoselin and Kleine-Vehn, Jürgen and Jallais, Yvon and Somssich, Marc},
	month = jan,
	year = {2022},
	keywords = {arabidopsis, casparian strip, endodermis, microdomains, neprosin, network},
	pages = {e69602},
}



Efficient uptake of nutrients in both animal and plant cells requires tissue-spanning diffusion barriers separating inner tissues from the outer lumen/soil. However, we poorly understand how such contiguous three-dimensional superstructures are formed in plants. Here, we show that correct establishment of the plant Casparian Strip (CS) network relies on local neighbor communication. We show that positioning of Casparian Strip membrane domains (CSDs) is tightly coordinated between neighbors in wild-type and that restriction of domain formation involves the putative extracellular protease LOTR1. Impaired domain restriction in lotr1 leads to fully functional CSDs at ectopic positions, forming ‘half strips’. LOTR1 action in the endodermis requires its expression in the stele. LOTR1 endodermal expression cannot complement, while cortex expression causes a dominant-negative phenotype. Our findings establish LOTR1 as a crucial player in CSD positioning acting in a directional, non-cell-autonomous manner to restrict and coordinate CS positioning.
Extracellular vesiculo-tubular structures associated with suberin deposition in plant cell walls. De Bellis, D., Kalmbach, L., Marhavý, P., Daraspe, J., Geldner, N., & Barberon, M. Nature Communications, 13(1): 1489. March 2022. Number: 1 Publisher: Nature Publishing Group
Extracellular vesiculo-tubular structures associated with suberin deposition in plant cell walls [link]Paper   doi   link   bibtex   abstract  
@article{de_bellis_extracellular_2022,
	title = {Extracellular vesiculo-tubular structures associated with suberin deposition in plant cell walls},
	volume = {13},
	copyright = {2022 The Author(s)},
	issn = {2041-1723},
	url = {https://www.nature.com/articles/s41467-022-29110-0},
	doi = {10.1038/s41467-022-29110-0},
	abstract = {Suberin is a fundamental plant biopolymer, found in protective tissues, such as seed coats, exodermis and endodermis of roots. Suberin is deposited in most suberizing cells in the form of lamellae just outside of the plasma membrane, below the primary cell wall. How monomeric suberin precursors, thought to be synthesized at the endoplasmic reticulum, are transported outside of the cell, for polymerization into suberin lamellae has remained obscure. Using electron-microscopy, we observed large numbers of extracellular vesiculo-tubular structures (EVs) to accumulate specifically in suberizing cells, in both chemically and cryo-fixed samples. EV presence correlates perfectly with root suberization and we could block suberin deposition and vesicle accumulation by affecting early, as well as late steps in the secretory pathway. Whereas many previous reports have described EVs in the context of biotic interactions, our results suggest a developmental role for extracellular vesicles in the formation of a major cell wall polymer.},
	language = {en},
	number = {1},
	urldate = {2024-02-08},
	journal = {Nature Communications},
	author = {De Bellis, Damien and Kalmbach, Lothar and Marhavý, Peter and Daraspe, Jean and Geldner, Niko and Barberon, Marie},
	month = mar,
	year = {2022},
	note = {Number: 1
Publisher: Nature Publishing Group},
	keywords = {Plant cell biology, Plant development},
	pages = {1489},
}



Suberin is a fundamental plant biopolymer, found in protective tissues, such as seed coats, exodermis and endodermis of roots. Suberin is deposited in most suberizing cells in the form of lamellae just outside of the plasma membrane, below the primary cell wall. How monomeric suberin precursors, thought to be synthesized at the endoplasmic reticulum, are transported outside of the cell, for polymerization into suberin lamellae has remained obscure. Using electron-microscopy, we observed large numbers of extracellular vesiculo-tubular structures (EVs) to accumulate specifically in suberizing cells, in both chemically and cryo-fixed samples. EV presence correlates perfectly with root suberization and we could block suberin deposition and vesicle accumulation by affecting early, as well as late steps in the secretory pathway. Whereas many previous reports have described EVs in the context of biotic interactions, our results suggest a developmental role for extracellular vesicles in the formation of a major cell wall polymer.
RNA Isolation from Nematode-Induced Feeding Sites in Arabidopsis RootsRoots Using Laser Capture Microdissection. Anjam, M. S., Siddique, S., & Marhavý, P. In Duque, P., & Szakonyi, D., editor(s), Environmental Responses in Plants: Methods and Protocols, of Methods in Molecular Biology, pages 313–324. Springer US, New York, NY, 2022.
RNA Isolation from Nematode-Induced Feeding Sites in Arabidopsis RootsRoots Using Laser Capture Microdissection [link]Paper   link   bibtex   abstract  
@incollection{anjam_rna_2022,
	address = {New York, NY},
	series = {Methods in {Molecular} {Biology}},
	title = {{RNA} {Isolation} from {Nematode}-{Induced} {Feeding} {Sites} in {Arabidopsis} {RootsRoots} {Using} {Laser} {Capture} {Microdissection}},
	isbn = {978-1-07-162297-1},
	url = {https://doi.org/10.1007/978-1-0716-2297-1_22},
	abstract = {Nematodes are diverse multicellular organisms that are most abundantly found in the soil. Most nematodes are free-living and feed on a range of organisms. Based on their feeding habits, soil nematodes can be classified into four groups: bacterial, omnivorous, fungal, and plant-feeding. Plant-parasitic nematodes (PPNs) are a serious threat to global food security, causing substantial losses to the agricultural sector. Root-knot and cyst nematodes are the most important of PPNs, significantly limiting the yield of commercial crops such as sugar beet, mustard, and cauliflower. The life cycle of these nematodes consists of four molting stages (J1–J4) that precede adulthood. Nonetheless, only second-stage juveniles (J2), which hatch from eggs, are infective worms that can parasitize the host’s roots. The freshly hatched juveniles (J2) of beet cyst nematode, Heterodera schachtii, establish a permanent feeding site inside the roots of the host plant. A cocktail of proteinaceous secretions is injected into a selected cell which later develops into a syncytium via local cell wall dissolution of several hundred neighboring cells. The formation of syncytium is accompanied by massive transcriptional, metabolic, and proteomic changes inside the host tissues. It creates a metabolic sink in which solutes are translocated to feed the nematodes throughout their life cycle. Deciphering the molecular signaling cascades during syncytium establishment is thus essential in studying the plant-nematode interactions and ensuring sustainability in agricultural practices. However, isolating RNA, protein, and metabolites from syncytial cells remains challenging. Extensive use of laser capture microdissection (LCM) in animal and human tissues has shown this approach to be a powerful technique for isolating a single cell from complex tissues. Here, we describe a simplified protocol for Arabidopsis-Heterodera schachtii infection assays, which is routinely applied in several plant-nematode laboratories. Next, we provide a detailed protocol for isolating high-quality RNA from syncytial cells induced by Heterodera schachtii in the roots of Arabidopsis thaliana plants.},
	language = {en},
	urldate = {2022-04-29},
	booktitle = {Environmental {Responses} in {Plants}: {Methods} and {Protocols}},
	publisher = {Springer US},
	author = {Anjam, Muhammad Shahzad and Siddique, Shahid and Marhavý, Peter},
	editor = {Duque, Paula and Szakonyi, Dóra},
	year = {2022},
	keywords = {Arabidopsis root dissection, Laser capture dissection, Plant-nematode infection, RNA extraction, Syncytial cell isolation},
	pages = {313--324},
}



Nematodes are diverse multicellular organisms that are most abundantly found in the soil. Most nematodes are free-living and feed on a range of organisms. Based on their feeding habits, soil nematodes can be classified into four groups: bacterial, omnivorous, fungal, and plant-feeding. Plant-parasitic nematodes (PPNs) are a serious threat to global food security, causing substantial losses to the agricultural sector. Root-knot and cyst nematodes are the most important of PPNs, significantly limiting the yield of commercial crops such as sugar beet, mustard, and cauliflower. The life cycle of these nematodes consists of four molting stages (J1–J4) that precede adulthood. Nonetheless, only second-stage juveniles (J2), which hatch from eggs, are infective worms that can parasitize the host’s roots. The freshly hatched juveniles (J2) of beet cyst nematode, Heterodera schachtii, establish a permanent feeding site inside the roots of the host plant. A cocktail of proteinaceous secretions is injected into a selected cell which later develops into a syncytium via local cell wall dissolution of several hundred neighboring cells. The formation of syncytium is accompanied by massive transcriptional, metabolic, and proteomic changes inside the host tissues. It creates a metabolic sink in which solutes are translocated to feed the nematodes throughout their life cycle. Deciphering the molecular signaling cascades during syncytium establishment is thus essential in studying the plant-nematode interactions and ensuring sustainability in agricultural practices. However, isolating RNA, protein, and metabolites from syncytial cells remains challenging. Extensive use of laser capture microdissection (LCM) in animal and human tissues has shown this approach to be a powerful technique for isolating a single cell from complex tissues. Here, we describe a simplified protocol for Arabidopsis-Heterodera schachtii infection assays, which is routinely applied in several plant-nematode laboratories. Next, we provide a detailed protocol for isolating high-quality RNA from syncytial cells induced by Heterodera schachtii in the roots of Arabidopsis thaliana plants.
  2021 (1)
Pickle Recruits Retinoblastoma Related 1 to Control Lateral Root Formation in Arabidopsis. Ötvös, K., Miskolczi, P., Marhavý, P., Cruz-Ramírez, A., Benková, E., Robert, S., & Bakó, L. International Journal of Molecular Sciences, 22(8): 3862. January 2021.
Pickle Recruits Retinoblastoma Related 1 to Control Lateral Root Formation in Arabidopsis [link]Paper   doi   link   bibtex   abstract   8 downloads  
@article{otvos_pickle_2021,
	title = {Pickle {Recruits} {Retinoblastoma} {Related} 1 to {Control} {Lateral} {Root} {Formation} in {Arabidopsis}},
	volume = {22},
	copyright = {http://creativecommons.org/licenses/by/3.0/},
	url = {https://www.mdpi.com/1422-0067/22/8/3862},
	doi = {10.3390/ijms22083862},
	abstract = {Lateral root (LR) formation is an example of a plant post-embryonic organogenesis event. LRs are issued from non-dividing cells entering consecutive steps of formative divisions, proliferation and elongation. The chromatin remodeling protein PICKLE (PKL) negatively regulates auxin-mediated LR formation through a mechanism that is not yet known. Here we show that PKL interacts with RETINOBLASTOMA-RELATED 1 (RBR1) to repress the LATERAL ORGAN BOUNDARIES-DOMAIN 16 (LBD16) promoter activity. Since LBD16 function is required for the formative division of LR founder cells, repression mediated by the PKL–RBR1 complex negatively regulates formative division and LR formation. Inhibition of LR formation by PKL–RBR1 is counteracted by auxin, indicating that, in addition to auxin-mediated transcriptional responses, the fine-tuned process of LR formation is also controlled at the chromatin level in an auxin-signaling dependent manner.},
	language = {en},
	number = {8},
	urldate = {2021-07-01},
	journal = {International Journal of Molecular Sciences},
	author = {Ötvös, Krisztina and Miskolczi, Pál and Marhavý, Peter and Cruz-Ramírez, Alfredo and Benková, Eva and Robert, Stéphanie and Bakó, László},
	month = jan,
	year = {2021},
	keywords = {\textit{de novo} organogenesis, auxin signaling, chromatin remodeling},
	pages = {3862},
}



Lateral root (LR) formation is an example of a plant post-embryonic organogenesis event. LRs are issued from non-dividing cells entering consecutive steps of formative divisions, proliferation and elongation. The chromatin remodeling protein PICKLE (PKL) negatively regulates auxin-mediated LR formation through a mechanism that is not yet known. Here we show that PKL interacts with RETINOBLASTOMA-RELATED 1 (RBR1) to repress the LATERAL ORGAN BOUNDARIES-DOMAIN 16 (LBD16) promoter activity. Since LBD16 function is required for the formative division of LR founder cells, repression mediated by the PKL–RBR1 complex negatively regulates formative division and LR formation. Inhibition of LR formation by PKL–RBR1 is counteracted by auxin, indicating that, in addition to auxin-mediated transcriptional responses, the fine-tuned process of LR formation is also controlled at the chromatin level in an auxin-signaling dependent manner.
  2020 (3)
Co-incidence of Damage and Microbial Patterns Controls Localized Immune Responses in Roots. Zhou, F., Emonet, A., Dénervaud Tendon, V., Marhavý, P., Wu, D., Lahaye, T., & Geldner, N. Cell, 180(3): 440–453.e18. February 2020.
Co-incidence of Damage and Microbial Patterns Controls Localized Immune Responses in Roots [link]Paper   doi   link   bibtex  
@article{zhou_co-incidence_2020,
	title = {Co-incidence of {Damage} and {Microbial} {Patterns} {Controls} {Localized} {Immune} {Responses} in {Roots}},
	volume = {180},
	issn = {00928674},
	url = {https://linkinghub.elsevier.com/retrieve/pii/S009286742030060X},
	doi = {10.1016/j.cell.2020.01.013},
	language = {en},
	number = {3},
	urldate = {2021-06-07},
	journal = {Cell},
	author = {Zhou, Feng and Emonet, Aurélia and Dénervaud Tendon, Valérie and Marhavý, Peter and Wu, Dousheng and Lahaye, Thomas and Geldner, Niko},
	month = feb,
	year = {2020},
	pages = {440--453.e18},
}



Cytokinin fluoroprobe reveals multiple sites of cytokinin perception at plasma membrane and endoplasmic reticulum. Kubiasová, K., Montesinos, J. C., Šamajová, O., Nisler, J., Mik, V., Semerádová, H., Plíhalová, L., Novák, O., Marhavý, P., Cavallari, N., Zalabák, D., Berka, K., Doležal, K., Galuszka, P., Šamaj, J., Strnad, M., Benková, E., Plíhal, O., & Spíchal, L. Nature Communications, 11(1): 4285. December 2020.
Cytokinin fluoroprobe reveals multiple sites of cytokinin perception at plasma membrane and endoplasmic reticulum [link]Paper   doi   link   bibtex   3 downloads  
@article{kubiasova_cytokinin_2020,
	title = {Cytokinin fluoroprobe reveals multiple sites of cytokinin perception at plasma membrane and endoplasmic reticulum},
	volume = {11},
	issn = {2041-1723},
	url = {http://www.nature.com/articles/s41467-020-17949-0},
	doi = {10.1038/s41467-020-17949-0},
	language = {en},
	number = {1},
	urldate = {2021-06-07},
	journal = {Nature Communications},
	author = {Kubiasová, Karolina and Montesinos, Juan Carlos and Šamajová, Olga and Nisler, Jaroslav and Mik, Václav and Semerádová, Hana and Plíhalová, Lucie and Novák, Ondřej and Marhavý, Peter and Cavallari, Nicola and Zalabák, David and Berka, Karel and Doležal, Karel and Galuszka, Petr and Šamaj, Jozef and Strnad, Miroslav and Benková, Eva and Plíhal, Ondřej and Spíchal, Lukáš},
	month = dec,
	year = {2020},
	pages = {4285},
}



SCHENGEN receptor module drives localized ROS production and lignification in plant roots. Fujita, S., De Bellis, D., Edel, K. H, Köster, P., Andersen, T. G., Schmid-Siegert, E., Dénervaud Tendon, V., Pfister, A., Marhavý, P., Ursache, R., Doblas, V. G, Barberon, M., Daraspe, J., Creff, A., Ingram, G., Kudla, J., & Geldner, N. The EMBO Journal, 39(9): e103894. May 2020. Publisher: John Wiley & Sons, Ltd
SCHENGEN receptor module drives localized ROS production and lignification in plant roots [link]Paper   doi   link   bibtex   abstract   2 downloads  
@article{fujita_schengen_2020,
	title = {{SCHENGEN} receptor module drives localized {ROS} production and lignification in plant roots},
	volume = {39},
	issn = {0261-4189},
	url = {https://www.embopress.org/doi/full/10.15252/embj.2019103894},
	doi = {10/gjct3x},
	abstract = {Abstract Production of reactive oxygen species (ROS) by NADPH oxidases (NOXs) impacts many processes in animals and plants, and many plant receptor pathways involve rapid, NOX-dependent increases of ROS. Yet, their general reactivity has made it challenging to pinpoint the precise role and immediate molecular action of ROS. A well-understood ROS action in plants is to provide the co-substrate for lignin peroxidases in the cell wall. Lignin can be deposited with exquisite spatial control, but the underlying mechanisms have remained elusive. Here, we establish a kinase signaling relay that exerts direct, spatial control over ROS production and lignification within the cell wall. We show that polar localization of a single kinase component is crucial for pathway function. Our data indicate that an intersection of more broadly localized components allows for micrometer-scale precision of lignification and that this system is triggered through initiation of ROS production as a critical peroxidase co-substrate.},
	number = {9},
	urldate = {2021-06-21},
	journal = {The EMBO Journal},
	author = {Fujita, Satoshi and De Bellis, Damien and Edel, Kai H and Köster, Philipp and Andersen, Tonni Grube and Schmid-Siegert, Emanuel and Dénervaud Tendon, Valérie and Pfister, Alexandre and Marhavý, Peter and Ursache, Robertas and Doblas, Verónica G and Barberon, Marie and Daraspe, Jean and Creff, Audrey and Ingram, Gwyneth and Kudla, Jörg and Geldner, Niko},
	month = may,
	year = {2020},
	note = {Publisher: John Wiley \& Sons, Ltd},
	keywords = {Casparian strips, extracellular diffusion barriers, lignin, localized ROS production, polarized signaling},
	pages = {e103894},
}



Abstract Production of reactive oxygen species (ROS) by NADPH oxidases (NOXs) impacts many processes in animals and plants, and many plant receptor pathways involve rapid, NOX-dependent increases of ROS. Yet, their general reactivity has made it challenging to pinpoint the precise role and immediate molecular action of ROS. A well-understood ROS action in plants is to provide the co-substrate for lignin peroxidases in the cell wall. Lignin can be deposited with exquisite spatial control, but the underlying mechanisms have remained elusive. Here, we establish a kinase signaling relay that exerts direct, spatial control over ROS production and lignification within the cell wall. We show that polar localization of a single kinase component is crucial for pathway function. Our data indicate that an intersection of more broadly localized components allows for micrometer-scale precision of lignification and that this system is triggered through initiation of ROS production as a critical peroxidase co-substrate.
  2019 (4)
A SOSEKI-based coordinate system interprets global polarity cues in Arabidopsis. Yoshida, S., van der Schuren, A., van Dop, M., van Galen, L., Saiga, S., Adibi, M., Möller, B., ten Hove, C. A., Marhavý, P., Smith, R., Friml, J., & Weijers, D. Nature Plants, 5(2): 160–166. February 2019.
A SOSEKI-based coordinate system interprets global polarity cues in Arabidopsis [link]Paper   doi   link   bibtex  
@article{yoshida_soseki-based_2019,
	title = {A {SOSEKI}-based coordinate system interprets global polarity cues in {Arabidopsis}},
	volume = {5},
	issn = {2055-0278},
	url = {http://www.nature.com/articles/s41477-019-0363-6},
	doi = {10/gfvgd3},
	language = {en},
	number = {2},
	urldate = {2021-06-07},
	journal = {Nature Plants},
	author = {Yoshida, Saiko and van der Schuren, Alja and van Dop, Maritza and van Galen, Luc and Saiga, Shunsuke and Adibi, Milad and Möller, Barbara and ten Hove, Colette A. and Marhavý, Peter and Smith, Richard and Friml, Jiri and Weijers, Dolf},
	month = feb,
	year = {2019},
	pages = {160--166},
}



Re-activation of Stem Cell Pathways for Pattern Restoration in Plant Wound Healing. Marhava, P., Hoermayer, L., Yoshida, S., Marhavý, P., Benková, E., & Friml, J. Cell, 177(4): 957–969.e13. May 2019.
Re-activation of Stem Cell Pathways for Pattern Restoration in Plant Wound Healing [link]Paper   doi   link   bibtex   4 downloads  
@article{marhava_re-activation_2019,
	title = {Re-activation of {Stem} {Cell} {Pathways} for {Pattern} {Restoration} in {Plant} {Wound} {Healing}},
	volume = {177},
	issn = {00928674},
	url = {https://linkinghub.elsevier.com/retrieve/pii/S0092867419304015},
	doi = {10/gfz9tc},
	language = {en},
	number = {4},
	urldate = {2021-06-07},
	journal = {Cell},
	author = {Marhava, Petra and Hoermayer, Lukas and Yoshida, Saiko and Marhavý, Peter and Benková, Eva and Friml, Jiří},
	month = may,
	year = {2019},
	pages = {957--969.e13},
}



Root endodermal barrier system contributes to defence against plant‐parasitic cyst and root‐knot nematodes. Holbein, J., Franke, R. B., Marhavý, P., Fujita, S., Górecka, M., Sobczak, M., Geldner, N., Schreiber, L., Grundler, F. M. W., & Siddique, S. The Plant Journal, 100(2): 221–236. October 2019.
Root endodermal barrier system contributes to defence against plant‐parasitic cyst and root‐knot nematodes [link]Paper   doi   link   bibtex   4 downloads  
@article{holbein_root_2019,
	title = {Root endodermal barrier system contributes to defence against plant‐parasitic cyst and root‐knot nematodes},
	volume = {100},
	issn = {0960-7412, 1365-313X},
	url = {https://onlinelibrary.wiley.com/doi/abs/10.1111/tpj.14459},
	doi = {10.1111/tpj.14459},
	language = {en},
	number = {2},
	urldate = {2021-06-07},
	journal = {The Plant Journal},
	author = {Holbein, Julia and Franke, Rochus B. and Marhavý, Peter and Fujita, Satoshi and Górecka, Mirosława and Sobczak, Mirosław and Geldner, Niko and Schreiber, Lukas and Grundler, Florian M. W. and Siddique, Shahid},
	month = oct,
	year = {2019},
	pages = {221--236},
}











Single‐cell damage elicits regional, nematode‐restricting ethylene responses in roots. Marhavý, P., Kurenda, A., Siddique, S., Dénervaud Tendon, V., Zhou, F., Holbein, J., Hasan, M S., Grundler, F. M., Farmer, E. E, & Geldner, N. The EMBO Journal, 38(10). May 2019.
Single‐cell damage elicits regional, nematode‐restricting ethylene responses in roots [link]Paper   doi   link   bibtex   7 downloads  
@article{marhavy_singlecell_2019,
	title = {Single‐cell damage elicits regional, nematode‐restricting ethylene responses in roots},
	volume = {38},
	issn = {0261-4189, 1460-2075},
	url = {https://onlinelibrary.wiley.com/doi/10.15252/embj.2018100972},
	doi = {10/gf2hvf},
	language = {en},
	number = {10},
	urldate = {2021-06-07},
	journal = {The EMBO Journal},
	author = {Marhavý, Peter and Kurenda, Andrzej and Siddique, Shahid and Dénervaud Tendon, Valerie and Zhou, Feng and Holbein, Julia and Hasan, M Shamim and Grundler, Florian MW and Farmer, Edward E and Geldner, Niko},
	month = may,
	year = {2019},
}



  2018 (2)
A protocol for combining fluorescent proteins with histological stains for diverse cell wall components. Ursache, R., Andersen, T. G., Marhavý, P., & Geldner, N. The Plant Journal, 93(2): 399–412. January 2018.
A protocol for combining fluorescent proteins with histological stains for diverse cell wall components [link]Paper   doi   link   bibtex  
@article{ursache_protocol_2018,
	title = {A protocol for combining fluorescent proteins with histological stains for diverse cell wall components},
	volume = {93},
	issn = {0960-7412, 1365-313X},
	url = {https://onlinelibrary.wiley.com/doi/abs/10.1111/tpj.13784},
	doi = {10/gkf56d},
	language = {en},
	number = {2},
	urldate = {2021-06-07},
	journal = {The Plant Journal},
	author = {Ursache, Robertas and Andersen, Tonni Grube and Marhavý, Peter and Geldner, Niko},
	month = jan,
	year = {2018},
	pages = {399--412},
}



Minimum requirements for changing and maintaining endodermis cell identity in the Arabidopsis root. Drapek, C., Sparks, E. E., Marhavý, P., Taylor, I., Andersen, T. G., Hennacy, J. H., Geldner, N., & Benfey, P. N. Nature Plants, 4(8): 586–595. August 2018.
Minimum requirements for changing and maintaining endodermis cell identity in the Arabidopsis root [link]Paper   doi   link   bibtex  
@article{drapek_minimum_2018,
	title = {Minimum requirements for changing and maintaining endodermis cell identity in the {Arabidopsis} root},
	volume = {4},
	issn = {2055-0278},
	url = {http://www.nature.com/articles/s41477-018-0213-y},
	doi = {10/gd9kpt},
	language = {en},
	number = {8},
	urldate = {2021-06-07},
	journal = {Nature Plants},
	author = {Drapek, Colleen and Sparks, Erin E. and Marhavý, Peter and Taylor, Isaiah and Andersen, Tonni G. and Hennacy, Jessica H. and Geldner, Niko and Benfey, Philip N.},
	month = aug,
	year = {2018},
	pages = {586--595},
}



  2016 (1)
Targeted cell elimination reveals an auxin-guided biphasic mode of lateral root initiation. Marhavý, P., Montesinos, J. C., Abuzeineh, A., Van Damme, D., Vermeer, J. E., Duclercq, J., Rakusová, H., Nováková, P., Friml, J., Geldner, N., & Benková, E. Genes & Development, 30(4): 471–483. February 2016.
Targeted cell elimination reveals an auxin-guided biphasic mode of lateral root initiation [link]Paper   doi   link   bibtex   7 downloads  
@article{marhavy_targeted_2016,
	title = {Targeted cell elimination reveals an auxin-guided biphasic mode of lateral root initiation},
	volume = {30},
	issn = {0890-9369, 1549-5477},
	url = {http://genesdev.cshlp.org/lookup/doi/10.1101/gad.276964.115},
	doi = {10.1101/gad.276964.115},
	language = {en},
	number = {4},
	urldate = {2021-06-07},
	journal = {Genes \& Development},
	author = {Marhavý, Peter and Montesinos, Juan Carlos and Abuzeineh, Anas and Van Damme, Daniel and Vermeer, Joop E.M. and Duclercq, Jerôme and Rakusová, Hana and Nováková, Petra and Friml, Jiři and Geldner, Niko and Benková, Eva},
	month = feb,
	year = {2016},
	keywords = {auxin, lateral root organogenesis, mechanical forces, meristem proliferation activity},
	pages = {471--483},
}







  2015 (3)
A coherent transcriptional feed-forward motif model for mediating auxin-sensitive PIN3 expression during lateral root development. Chen, Q., Liu, Y., Maere, S., Lee, E., Van Isterdael, G., Xie, Z., Xuan, W., Lucas, J., Vassileva, V., Kitakura, S., Marhavý, P., Wabnik, K., Geldner, N., Benkova, E., Le, J., Fukaki, H., Grotewold, E., Li, C., Friml, J., Sack, F., Beeckman, T., & Vanneste, S. Nat Commun, 6(1): 8821. November 2015.
A coherent transcriptional feed-forward motif model for mediating auxin-sensitive PIN3 expression during lateral root development [link]Paper   doi   link   bibtex   abstract  
@article{chen_coherent_2015,
	title = {A coherent transcriptional feed-forward motif model for mediating auxin-sensitive {PIN3} expression during lateral root development},
	volume = {6},
	issn = {2041-1723 (Electronic) 2041-1723 (Linking)},
	url = {https://www.ncbi.nlm.nih.gov/pubmed/26578065},
	doi = {10.1038/ncomms9821},
	abstract = {Multiple plant developmental processes, such as lateral root development, depend on auxin distribution patterns that are in part generated by the PIN-formed family of auxin-efflux transporters. Here we propose that AUXIN RESPONSE FACTOR7 (ARF7) and the ARF7-regulated FOUR LIPS/MYB124 (FLP) transcription factors jointly form a coherent feed-forward motif that mediates the auxin-responsive PIN3 transcription in planta to steer the early steps of lateral root formation. This regulatory mechanism might endow the PIN3 circuitry with a temporal 'memory' of auxin stimuli, potentially maintaining and enhancing the robustness of the auxin flux directionality during lateral root development. The cooperative action between canonical auxin signalling and other transcription factors might constitute a general mechanism by which transcriptional auxin-sensitivity can be regulated at a tissue-specific level.},
	language = {en},
	number = {1},
	urldate = {2021-06-07},
	journal = {Nat Commun},
	author = {Chen, Q. and Liu, Y. and Maere, S. and Lee, E. and Van Isterdael, G. and Xie, Z. and Xuan, W. and Lucas, J. and Vassileva, V. and Kitakura, S. and Marhavý, P. and Wabnik, K. and Geldner, N. and Benkova, E. and Le, J. and Fukaki, H. and Grotewold, E. and Li, C. and Friml, J. and Sack, F. and Beeckman, T. and Vanneste, S.},
	month = nov,
	year = {2015},
	keywords = {*Gene Expression Regulation, Plant, Arabidopsis Proteins/*genetics/metabolism, Arabidopsis/*genetics/growth \& development, Chromatin Immunoprecipitation, Feedback, Physiological, Glucuronidase/metabolism, Organisms, Genetically Modified, Plant Roots/*growth \& development/metabolism, RNA, Messenger/*metabolism, Reverse Transcriptase Polymerase Chain Reaction, Signal Transduction, Transcription Factors/*genetics/metabolism, Transcription, Genetic},
	pages = {8821},
}



Multiple plant developmental processes, such as lateral root development, depend on auxin distribution patterns that are in part generated by the PIN-formed family of auxin-efflux transporters. Here we propose that AUXIN RESPONSE FACTOR7 (ARF7) and the ARF7-regulated FOUR LIPS/MYB124 (FLP) transcription factors jointly form a coherent feed-forward motif that mediates the auxin-responsive PIN3 transcription in planta to steer the early steps of lateral root formation. This regulatory mechanism might endow the PIN3 circuitry with a temporal 'memory' of auxin stimuli, potentially maintaining and enhancing the robustness of the auxin flux directionality during lateral root development. The cooperative action between canonical auxin signalling and other transcription factors might constitute a general mechanism by which transcriptional auxin-sensitivity can be regulated at a tissue-specific level.
Cytokinin response factors regulate PIN-FORMED auxin transporters. Simaskova, M., O'Brien, J. A., Khan, M., Van Noorden, G., Otvos, K., Vieten, A., De Clercq, I., Van Haperen, J. M. A., Cuesta, C., Hoyerova, K., Vanneste, S., Marhavý, P., Wabnik, K., Van Breusegem, F., Nowack, M., Murphy, A., Friml, J., Weijers, D., Beeckman, T., & Benkova, E. Nat Commun, 6(1): 8717. November 2015. Edition: 2015/11/07
Cytokinin response factors regulate PIN-FORMED auxin transporters [link]Paper   doi   link   bibtex   abstract  
@article{simaskova_cytokinin_2015,
	title = {Cytokinin response factors regulate {PIN}-{FORMED} auxin transporters},
	volume = {6},
	issn = {2041-1723 (Electronic) 2041-1723 (Linking)},
	url = {https://www.ncbi.nlm.nih.gov/pubmed/26541513},
	doi = {10.1038/ncomms9717},
	abstract = {Auxin and cytokinin are key endogenous regulators of plant development. Although cytokinin-mediated modulation of auxin distribution is a developmentally crucial hormonal interaction, its molecular basis is largely unknown. Here we show a direct regulatory link between cytokinin signalling and the auxin transport machinery uncovering a mechanistic framework for cytokinin-auxin cross-talk. We show that the CYTOKININ RESPONSE FACTORS (CRFs), transcription factors downstream of cytokinin perception, transcriptionally control genes encoding PIN-FORMED (PIN) auxin transporters at a specific PIN CYTOKININ RESPONSE ELEMENT (PCRE) domain. Removal of this cis-regulatory element effectively uncouples PIN transcription from the CRF-mediated cytokinin regulation and attenuates plant cytokinin sensitivity. We propose that CRFs represent a missing cross-talk component that fine-tunes auxin transport capacity downstream of cytokinin signalling to control plant development.},
	language = {en},
	number = {1},
	urldate = {2021-06-07},
	journal = {Nat Commun},
	author = {Simaskova, M. and O'Brien, J. A. and Khan, M. and Van Noorden, G. and Otvos, K. and Vieten, A. and De Clercq, I. and Van Haperen, J. M. A. and Cuesta, C. and Hoyerova, K. and Vanneste, S. and Marhavý, P. and Wabnik, K. and Van Breusegem, F. and Nowack, M. and Murphy, A. and Friml, J. and Weijers, D. and Beeckman, T. and Benkova, E.},
	month = nov,
	year = {2015},
	note = {Edition: 2015/11/07},
	keywords = {Arabidopsis, Arabidopsis Proteins/*genetics/metabolism, Chromatin Immunoprecipitation, Cytokinins/*metabolism, Gene Expression Regulation, Plant, Green Fluorescent Proteins, Indoleacetic Acids/*metabolism, Membrane Transport Proteins/*genetics/metabolism, Microscopy, Confocal, Plant Roots/metabolism, Plants, Genetically Modified, Real-Time Polymerase Chain Reaction, Response Elements, Signal Transduction, Transcription Factors/*genetics/metabolism},
	pages = {8717},
}



Auxin and cytokinin are key endogenous regulators of plant development. Although cytokinin-mediated modulation of auxin distribution is a developmentally crucial hormonal interaction, its molecular basis is largely unknown. Here we show a direct regulatory link between cytokinin signalling and the auxin transport machinery uncovering a mechanistic framework for cytokinin-auxin cross-talk. We show that the CYTOKININ RESPONSE FACTORS (CRFs), transcription factors downstream of cytokinin perception, transcriptionally control genes encoding PIN-FORMED (PIN) auxin transporters at a specific PIN CYTOKININ RESPONSE ELEMENT (PCRE) domain. Removal of this cis-regulatory element effectively uncouples PIN transcription from the CRF-mediated cytokinin regulation and attenuates plant cytokinin sensitivity. We propose that CRFs represent a missing cross-talk component that fine-tunes auxin transport capacity downstream of cytokinin signalling to control plant development.
Real-time Analysis of Lateral Root Organogenesis in Arabidopsis. Marhavý, P., & Benkova, E. BIO-PROTOCOL, 5(8). 2015.
Real-time Analysis of Lateral Root Organogenesis in Arabidopsis [link]Paper   doi   link   bibtex  
@article{marhavy_real-time_2015,
	title = {Real-time {Analysis} of {Lateral} {Root} {Organogenesis} in {Arabidopsis}},
	volume = {5},
	issn = {2331-8325},
	url = {http://www.bio-protocol.org/e1446},
	doi = {10/ggsz3x},
	language = {en},
	number = {8},
	urldate = {2021-06-07},
	journal = {BIO-PROTOCOL},
	author = {Marhavý, Peter and Benkova, Eva},
	year = {2015},
}



  2014 (1)
Cytokinin Controls Polarity of PIN1-Dependent Auxin Transport during Lateral Root Organogenesis. Marhavý, P., Duclercq, J., Weller, B., Feraru, E., Bielach, A., Offringa, R., Friml, J., Schwechheimer, C., Murphy, A., & Benková, E. Current Biology, 24(9): 1031–1037. May 2014.
Cytokinin Controls Polarity of PIN1-Dependent Auxin Transport during Lateral Root Organogenesis [link]Paper   doi   link   bibtex   1 download  
@article{marhavy_cytokinin_2014,
	title = {Cytokinin {Controls} {Polarity} of {PIN1}-{Dependent} {Auxin} {Transport} during {Lateral} {Root} {Organogenesis}},
	volume = {24},
	issn = {09609822},
	url = {https://linkinghub.elsevier.com/retrieve/pii/S0960982214004023},
	doi = {10/f52zbg},
	language = {en},
	number = {9},
	urldate = {2021-06-08},
	journal = {Current Biology},
	author = {Marhavý, Peter and Duclercq, Jérôme and Weller, Benjamin and Feraru, Elena and Bielach, Agnieszka and Offringa, Remko and Friml, Jiří and Schwechheimer, Claus and Murphy, Angus and Benková, Eva},
	month = may,
	year = {2014},
	pages = {1031--1037},
}



  2013 (2)
An Auxin Transport Mechanism Restricts Positive Orthogravitropism in Lateral Roots. Rosquete, M., von Wangenheim , D., Marhavý, P., Barbez, E., Stelzer, E., Benková, E., Maizel, A., & Kleine-Vehn, J. Current Biology, 23(9): 817–822. May 2013.
An Auxin Transport Mechanism Restricts Positive Orthogravitropism in Lateral Roots [link]Paper   doi   link   bibtex   1 download  
@article{rosquete_auxin_2013,
	title = {An {Auxin} {Transport} {Mechanism} {Restricts} {Positive} {Orthogravitropism} in {Lateral} {Roots}},
	volume = {23},
	issn = {09609822},
	url = {https://linkinghub.elsevier.com/retrieve/pii/S0960982213003667},
	doi = {10/f4w5br},
	language = {en},
	number = {9},
	urldate = {2021-06-08},
	journal = {Current Biology},
	author = {Rosquete, Michel Ruiz and von Wangenheim, Daniel and Marhavý, Peter and Barbez, Elke and Stelzer, Ernst H.K. and Benková, Eva and Maizel, Alexis and Kleine-Vehn, Jürgen},
	month = may,
	year = {2013},
	pages = {817--822},
}



The protein quality control system manages plant defence compound synthesis. Pollier, J., Moses, T., González-Guzmán, M., De Geyter, N., Lippens, S., Vanden Bossche, R., Marhavý, P., Kremer, A., Morreel, K., Guérin, C. J., Tava, A., Oleszek, W., Thevelein, J. M., Campos, N., Goormachtig, S., & Goossens, A. Nature, 504(7478): 148–152. December 2013.
doi   link   bibtex   abstract  
@article{pollier_protein_2013,
	title = {The protein quality control system manages plant defence compound synthesis},
	volume = {504},
	issn = {1476-4687},
	doi = {10/f5jcsn},
	abstract = {Jasmonates are ubiquitous oxylipin-derived phytohormones that are essential in the regulation of many development, growth and defence processes. Across the plant kingdom, jasmonates act as elicitors of the production of bioactive secondary metabolites that serve in defence against attackers. Knowledge of the conserved jasmonate perception and early signalling machineries is increasing, but the downstream mechanisms that regulate defence metabolism remain largely unknown. Here we show that, in the legume Medicago truncatula, jasmonate recruits the endoplasmic-reticulum-associated degradation (ERAD) quality control system to manage the production of triterpene saponins, widespread bioactive compounds that share a biogenic origin with sterols. An ERAD-type RING membrane-anchor E3 ubiquitin ligase is co-expressed with saponin synthesis enzymes to control the activity of 3-hydroxy-3-methylglutaryl-CoA reductase (HMGR), the rate-limiting enzyme in the supply of the ubiquitous terpene precursor isopentenyl diphosphate. Thus, unrestrained bioactive saponin accumulation is prevented and plant development and integrity secured. This control apparatus is equivalent to the ERAD system that regulates sterol synthesis in yeasts and mammals but that uses distinct E3 ubiquitin ligases, of the HMGR degradation 1 (HRD1) type, to direct destruction of HMGR. Hence, the general principles for the management of sterol and triterpene saponin biosynthesis are conserved across eukaryotes but can be controlled by divergent regulatory cues.},
	language = {eng},
	number = {7478},
	journal = {Nature},
	author = {Pollier, Jacob and Moses, Tessa and González-Guzmán, Miguel and De Geyter, Nathan and Lippens, Saskia and Vanden Bossche, Robin and Marhavý, Peter and Kremer, Anna and Morreel, Kris and Guérin, Christopher J. and Tava, Aldo and Oleszek, Wieslaw and Thevelein, Johan M. and Campos, Narciso and Goormachtig, Sofie and Goossens, Alain},
	month = dec,
	year = {2013},
	pmid = {24213631},
	keywords = {Cells, Cultured, Endoplasmic Reticulum-Associated Degradation, Gene Expression Profiling, Gene Expression Regulation, Plant, Gene Silencing, Genetic Complementation Test, Medicago truncatula, Microscopy, Electron, Scanning, Molecular Sequence Data, Mutation, Plant Growth Regulators, Plant Roots, Saccharomyces cerevisiae, Saponins, Signal Transduction, Ubiquitin-Protein Ligases},
	pages = {148--152},
}















Jasmonates are ubiquitous oxylipin-derived phytohormones that are essential in the regulation of many development, growth and defence processes. Across the plant kingdom, jasmonates act as elicitors of the production of bioactive secondary metabolites that serve in defence against attackers. Knowledge of the conserved jasmonate perception and early signalling machineries is increasing, but the downstream mechanisms that regulate defence metabolism remain largely unknown. Here we show that, in the legume Medicago truncatula, jasmonate recruits the endoplasmic-reticulum-associated degradation (ERAD) quality control system to manage the production of triterpene saponins, widespread bioactive compounds that share a biogenic origin with sterols. An ERAD-type RING membrane-anchor E3 ubiquitin ligase is co-expressed with saponin synthesis enzymes to control the activity of 3-hydroxy-3-methylglutaryl-CoA reductase (HMGR), the rate-limiting enzyme in the supply of the ubiquitous terpene precursor isopentenyl diphosphate. Thus, unrestrained bioactive saponin accumulation is prevented and plant development and integrity secured. This control apparatus is equivalent to the ERAD system that regulates sterol synthesis in yeasts and mammals but that uses distinct E3 ubiquitin ligases, of the HMGR degradation 1 (HRD1) type, to direct destruction of HMGR. Hence, the general principles for the management of sterol and triterpene saponin biosynthesis are conserved across eukaryotes but can be controlled by divergent regulatory cues.
  2012 (3)
Auxin reflux between the endodermis and pericycle promotes lateral root initiation. Marhavý, P., Vanstraelen, M., De Rybel, B., Zhaojun, D., Bennett, M. J, Beeckman, T., & Benková, E. The EMBO Journal, 32(1): 149–158. November 2012.
Auxin reflux between the endodermis and pericycle promotes lateral root initiation [link]Paper   doi   link   bibtex  
@article{marhavy_auxin_2012,
	title = {Auxin reflux between the endodermis and pericycle promotes lateral root initiation},
	volume = {32},
	issn = {0261-4189, 1460-2075},
	url = {http://emboj.embopress.org/cgi/doi/10.1038/emboj.2012.303},
	doi = {10/gkgdj3},
	number = {1},
	urldate = {2021-06-08},
	journal = {The EMBO Journal},
	author = {Marhavý, Peter and Vanstraelen, Marleen and De Rybel, Bert and Zhaojun, Ding and Bennett, Malcolm J and Beeckman, Tom and Benková, Eva},
	month = nov,
	year = {2012},
	pages = {149--158},
}



Genetic approach towards the identification of auxin–cytokinin crosstalk components involved in root development. Bielach, A., Duclercq, J., Marhavý, P., & Benková, E. Philosophical Transactions of the Royal Society B: Biological Sciences, 367(1595): 1469–1478. June 2012. Publisher: Royal Society
Genetic approach towards the identification of auxin–cytokinin crosstalk components involved in root development [link]Paper   doi   link   bibtex   abstract   1 download  
@article{bielach_genetic_2012,
	title = {Genetic approach towards the identification of auxin–cytokinin crosstalk components involved in root development},
	volume = {367},
	url = {https://royalsocietypublishing.org/doi/10.1098/rstb.2011.0233},
	doi = {10/f32frv},
	abstract = {Phytohormones are important plant growth regulators that control many developmental processes, such as cell division, cell differentiation, organogenesis and morphogenesis. They regulate a multitude of apparently unrelated physiological processes, often with overlapping roles, and they mutually modulate their effects. These features imply important synergistic and antagonistic interactions between the various plant hormones. Auxin and cytokinin are central hormones involved in the regulation of plant growth and development, including processes determining root architecture, such as root pole establishment during early embryogenesis, root meristem maintenance and lateral root organogenesis. Thus, to control root development both pathways put special demands on the mechanisms that balance their activities and mediate their interactions. Here, we summarize recent knowledge on the role of auxin and cytokinin in the regulation of root architecture with special focus on lateral root organogenesis, discuss the latest findings on the molecular mechanisms of their interactions, and present forward genetic screen as a tool to identify novel molecular components of the auxin and cytokinin crosstalk.},
	number = {1595},
	urldate = {2021-06-08},
	journal = {Philosophical Transactions of the Royal Society B: Biological Sciences},
	author = {Bielach, Agnieszka and Duclercq, Jérôme and Marhavý, Peter and Benková, Eva},
	month = jun,
	year = {2012},
	note = {Publisher: Royal Society},
	pages = {1469--1478},
}







Phytohormones are important plant growth regulators that control many developmental processes, such as cell division, cell differentiation, organogenesis and morphogenesis. They regulate a multitude of apparently unrelated physiological processes, often with overlapping roles, and they mutually modulate their effects. These features imply important synergistic and antagonistic interactions between the various plant hormones. Auxin and cytokinin are central hormones involved in the regulation of plant growth and development, including processes determining root architecture, such as root pole establishment during early embryogenesis, root meristem maintenance and lateral root organogenesis. Thus, to control root development both pathways put special demands on the mechanisms that balance their activities and mediate their interactions. Here, we summarize recent knowledge on the role of auxin and cytokinin in the regulation of root architecture with special focus on lateral root organogenesis, discuss the latest findings on the molecular mechanisms of their interactions, and present forward genetic screen as a tool to identify novel molecular components of the auxin and cytokinin crosstalk.
Spatiotemporal Regulation of Lateral Root Organogenesis in Arabidopsis by Cytokinin. Bielach, A., Podlešáková, K., Marhavý, P., Duclercq, J., Cuesta, C., Müller, B., Grunewald, W., Tarkowski, P., & Benková, E. The Plant Cell, 24(10): 3967–3981. October 2012.
Spatiotemporal Regulation of Lateral Root Organogenesis in <i>Arabidopsis</i> by Cytokinin [link]Paper   doi   link   bibtex   1 download  
@article{bielach_spatiotemporal_2012,
	title = {Spatiotemporal {Regulation} of {Lateral} {Root} {Organogenesis} in \textit{{Arabidopsis}} by {Cytokinin}},
	volume = {24},
	issn = {1040-4651, 1532-298X},
	url = {https://academic.oup.com/plcell/article/24/10/3967-3981/6101532},
	doi = {10/f4ffx8},
	language = {en},
	number = {10},
	urldate = {2021-06-08},
	journal = {The Plant Cell},
	author = {Bielach, Agnieszka and Podlešáková, Kateřina and Marhavý, Peter and Duclercq, Jérôme and Cuesta, Candela and Müller, Bruno and Grunewald, Wim and Tarkowski, Petr and Benková, Eva},
	month = oct,
	year = {2012},
	pages = {3967--3981},
}



  2011 (1)
Cytokinin Modulates Endocytic Trafficking of PIN1 Auxin Efflux Carrier to Control Plant Organogenesis. Marhavý, P., Bielach, A., Abas, L., Abuzeineh, A., Duclercq, J., Tanaka, H., Pařezová, M., Petrášek, J., Friml, J., Kleine-Vehn, J., & Benková, E. Developmental Cell, 21(4): 796–804. October 2011.
Cytokinin Modulates Endocytic Trafficking of PIN1 Auxin Efflux Carrier to Control Plant Organogenesis [link]Paper   doi   link   bibtex  
@article{marhavy_cytokinin_2011,
	title = {Cytokinin {Modulates} {Endocytic} {Trafficking} of {PIN1} {Auxin} {Efflux} {Carrier} to {Control} {Plant} {Organogenesis}},
	volume = {21},
	issn = {15345807},
	url = {https://linkinghub.elsevier.com/retrieve/pii/S1534580711003522},
	doi = {10/bz65s4},
	language = {en},
	number = {4},
	urldate = {2021-06-08},
	journal = {Developmental Cell},
	author = {Marhavý, Peter and Bielach, Agnieszka and Abas, Lindy and Abuzeineh, Anas and Duclercq, Jerome and Tanaka, Hirokazu and Pařezová, Markéta and Petrášek, Jan and Friml, Jiří and Kleine-Vehn, Jürgen and Benková, Eva},
	month = oct,
	year = {2011},
	pages = {796--804},
}







  2010 (1)
Role of PIN-mediated auxin efflux in apical hook development of Arabidopsis thaliana. Žádníková, P., Petrášek, J., Marhavý, P., Raz, V., Vandenbussche, F., Ding, Z., Schwarzerová, K., Morita, M. T., Tasaka, M., Hejátko, J., Van Der Straeten, D., Friml, J., & Benková, E. Development, 137(4): 607–617. February 2010.
Role of PIN-mediated auxin efflux in apical hook development of <i>Arabidopsis thaliana</i> [link]Paper   doi   link   bibtex   abstract   2 downloads  
@article{zadnikova_role_2010,
	title = {Role of {PIN}-mediated auxin efflux in apical hook development of \textit{{Arabidopsis} thaliana}},
	volume = {137},
	issn = {1477-9129, 0950-1991},
	url = {https://journals.biologists.com/dev/article/137/4/607/44209/Role-of-PIN-mediated-auxin-efflux-in-apical-hook},
	doi = {10/cs9rb3},
	abstract = {The apical hook of dark-grown Arabidopsis seedlings is a simple structure that develops soon after germination to protect the meristem tissues during emergence through the soil and that opens upon exposure to light. Differential growth at the apical hook proceeds in three sequential steps that are regulated by multiple hormones, principally auxin and ethylene. We show that the progress of the apical hook through these developmental phases depends on the dynamic, asymmetric distribution of auxin, which is regulated by auxin efflux carriers of the PIN family. Several PIN proteins exhibited specific, partially overlapping spatial and temporal expression patterns, and their subcellular localization suggested auxin fluxes during hook development. Genetic manipulation of individual PIN activities interfered with different stages of hook development, implying that specific combinations of PIN genes are required for progress of the apical hook through the developmental phases. Furthermore, ethylene might modulate apical hook development by prolonging the formation phase and strongly suppressing the maintenance phase. This ethylene effect is in part mediated by regulation of PIN-dependent auxin efflux and auxin signaling.},
	language = {en},
	number = {4},
	urldate = {2021-06-08},
	journal = {Development},
	author = {Žádníková, Petra and Petrášek, Jan and Marhavý, Peter and Raz, Vered and Vandenbussche, Filip and Ding, Zhaojun and Schwarzerová, Kateřina and Morita, Miyo T. and Tasaka, Masao and Hejátko, Jan and Van Der Straeten, Dominique and Friml, Jiří and Benková, Eva},
	month = feb,
	year = {2010},
	pages = {607--617},
}



The apical hook of dark-grown Arabidopsis seedlings is a simple structure that develops soon after germination to protect the meristem tissues during emergence through the soil and that opens upon exposure to light. Differential growth at the apical hook proceeds in three sequential steps that are regulated by multiple hormones, principally auxin and ethylene. We show that the progress of the apical hook through these developmental phases depends on the dynamic, asymmetric distribution of auxin, which is regulated by auxin efflux carriers of the PIN family. Several PIN proteins exhibited specific, partially overlapping spatial and temporal expression patterns, and their subcellular localization suggested auxin fluxes during hook development. Genetic manipulation of individual PIN activities interfered with different stages of hook development, implying that specific combinations of PIN genes are required for progress of the apical hook through the developmental phases. Furthermore, ethylene might modulate apical hook development by prolonging the formation phase and strongly suppressing the maintenance phase. This ethylene effect is in part mediated by regulation of PIN-dependent auxin efflux and auxin signaling.
Portrait photo of Petra Marhava standing in an in vitro growth room fetching a square plate with green Arabidopsis seedlings

Marhava, Petra - Plant acclimation to heat and cold stress

Research

Portrait photo of Petra Marhava standing in an in vitro growth room fetching a square plate with green Arabidopsis seedlingsPhoto: Andreas Palmén

Temperatures below or above the physiological optimum for plant growth induce temperature stress, which can cause detrimental and irreversible damage to plant growth and development. While most of the studies to date have focused on big-picture elements of plant responses to climate change, our research will provide insights into the molecular and cellular responses, to improve our mechanistic understanding of plant acclimation to heat and cold stress.

Even though studies on the underlying mechanisms of plant acclimation to high/low temperature are making steady progress, many questions remain unanswered. In particular, the role of the plant root system during acclimation to temperature stress has received little attention, though temperature stress at the root level can strongly affect the function of the whole plant and decrease crop productivity. In addition, despite knowing that plants show organ-specific transcriptome responses to temperature stress, we still tend to generalize findings based on shoot tissues. In my group, we combine state-of-the-art techniques for exploring root tissue to understand how roots sense and modulate their growth in response to fluctuating temperatures.

Group Members

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    Anjam, Muhammad Shahzad
    PostDoc
    E-mail
    Room: B5-48-45
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    Basheer, Jasim
    PostDoc
    E-mail
    Room: C4-29-40
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    Cheng, Ling
    PostDoc
    E-mail
    Room: B5-52-45
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    Khakurel, Dhruba
    PostDoc
    E-mail
    Room: KB5C8
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    Sharma, Manvi
    PostDoc
    E-mail
    Room: B5-18-45
  • Personnel Image
    Zahid, Nageena
    PostDoc
    E-mail
    Room: C4-29-40

CV P. Marhava

  • 2022 – to date: Independent Researcher
Umeå Plant Science Center (UPSC), Department of Forest Genetics and Plant Physiology, Swedish University of Agricultural Sciences (SLU), Umeå, Sweden
  • 2020 – 2022: Researcher
Umeå Plant Science Center (UPSC), Department of Forest Genetics and Plant Physiology, Swedish University of Agricultural Sciences (SLU), Umeå, Sweden
  • 2015 – 2020: Postdoctoral researcher
University of Lausanne, Department of Molecular Biology of Plants (DBMV), Lausanne, Switzerland
Supervisor: Prof. Christian S. Hardtke
  • 2011 – 2015: Doctor of Philosophy (Ph.D.)
Institute of Science and Technology in Austria (IST Austria), Austria
VIB Department of Plant Systems Biology, Ghent University, Belgium
Supervisor: Prof. Jiří Friml

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  2024 (2)
Ectopic assembly of an auxin efflux control machinery shifts developmental trajectories. Aliaga Fandino, A. C., Jelínková, A., Marhava, P., Petrášek, J., & Hardtke, C. S The Plant Cell, 36(5): 1791–1805. May 2024.
Ectopic assembly of an auxin efflux control machinery shifts developmental trajectories [link]Paper   doi   link   bibtex   abstract  
@article{aliaga_fandino_ectopic_2024,
	title = {Ectopic assembly of an auxin efflux control machinery shifts developmental trajectories},
	volume = {36},
	issn = {1040-4651},
	url = {https://doi.org/10.1093/plcell/koae023},
	doi = {10.1093/plcell/koae023},
	abstract = {Polar auxin transport in the Arabidopsis (Arabidopsis thaliana) root tip maintains high auxin levels around the stem cell niche that gradually decrease in dividing cells but increase again once they transition toward differentiation. Protophloem differentiates earlier than other proximal tissues and employs a unique auxin “canalization” machinery that is thought to balance auxin efflux with retention. It consists of a proposed activator of PIN-FORMED (PIN) auxin efflux carriers, the cAMP-, cGMP- and Calcium-dependent (AGC) kinase PROTEIN KINASE ASSOCIATED WITH BRX (PAX); its inhibitor, BREVIS RADIX (BRX); and PHOSPHATIDYLINOSITOL-4-PHOSPHATE-5-KINASE (PIP5K) enzymes, which promote polar PAX and BRX localization. Because of a dynamic PAX–BRX–PIP5K interplay, the net cellular output of this machinery remains unclear. In this study, we deciphered the dosage-sensitive regulatory interactions among PAX, BRX, and PIP5K by their ectopic expression in developing xylem vessels. The data suggest that the dominant collective output of the PAX–BRX–PIP5K module is a localized reduction in PIN abundance. This requires PAX-stimulated clathrin-mediated PIN endocytosis upon site-specific phosphorylation, which distinguishes PAX from other AGC kinases. An ectopic assembly of the PAX–BRX–PIP5K module is sufficient to cause cellular auxin retention and affects root growth vigor by accelerating the trajectory of xylem vessel development. Our data thus provide direct evidence that local manipulation of auxin efflux alters the timing of cellular differentiation in the root.},
	number = {5},
	urldate = {2024-10-02},
	journal = {The Plant Cell},
	author = {Aliaga Fandino, Ana Cecilia and Jelínková, Adriana and Marhava, Petra and Petrášek, Jan and Hardtke, Christian S},
	month = may,
	year = {2024},
	pages = {1791--1805},
}















Polar auxin transport in the Arabidopsis (Arabidopsis thaliana) root tip maintains high auxin levels around the stem cell niche that gradually decrease in dividing cells but increase again once they transition toward differentiation. Protophloem differentiates earlier than other proximal tissues and employs a unique auxin “canalization” machinery that is thought to balance auxin efflux with retention. It consists of a proposed activator of PIN-FORMED (PIN) auxin efflux carriers, the cAMP-, cGMP- and Calcium-dependent (AGC) kinase PROTEIN KINASE ASSOCIATED WITH BRX (PAX); its inhibitor, BREVIS RADIX (BRX); and PHOSPHATIDYLINOSITOL-4-PHOSPHATE-5-KINASE (PIP5K) enzymes, which promote polar PAX and BRX localization. Because of a dynamic PAX–BRX–PIP5K interplay, the net cellular output of this machinery remains unclear. In this study, we deciphered the dosage-sensitive regulatory interactions among PAX, BRX, and PIP5K by their ectopic expression in developing xylem vessels. The data suggest that the dominant collective output of the PAX–BRX–PIP5K module is a localized reduction in PIN abundance. This requires PAX-stimulated clathrin-mediated PIN endocytosis upon site-specific phosphorylation, which distinguishes PAX from other AGC kinases. An ectopic assembly of the PAX–BRX–PIP5K module is sufficient to cause cellular auxin retention and affects root growth vigor by accelerating the trajectory of xylem vessel development. Our data thus provide direct evidence that local manipulation of auxin efflux alters the timing of cellular differentiation in the root.
Mechanical forces in plant tissue matrix orient cell divisions via microtubule stabilization. Hoermayer, L., Montesinos, J. C., Trozzi, N., Spona, L., Yoshida, S., Marhava, P., Caballero-Mancebo, S., Benková, E., Heisenberg, C., Dagdas, Y., Majda, M., & Friml, J. Developmental Cell, 59(10): 1333–1344.e4. May 2024.
Mechanical forces in plant tissue matrix orient cell divisions via microtubule stabilization [link]Paper   doi   link   bibtex   abstract  
@article{hoermayer_mechanical_2024,
	title = {Mechanical forces in plant tissue matrix orient cell divisions via microtubule stabilization},
	volume = {59},
	issn = {1534-5807},
	url = {https://www.sciencedirect.com/science/article/pii/S1534580724001771},
	doi = {10.1016/j.devcel.2024.03.009},
	abstract = {Plant morphogenesis relies exclusively on oriented cell expansion and division. Nonetheless, the mechanism(s) determining division plane orientation remain elusive. Here, we studied tissue healing after laser-assisted wounding in roots of Arabidopsis thaliana and uncovered how mechanical forces stabilize and reorient the microtubule cytoskeleton for the orientation of cell division. We identified that root tissue functions as an interconnected cell matrix, with a radial gradient of tissue extendibility causing predictable tissue deformation after wounding. This deformation causes instant redirection of expansion in the surrounding cells and reorientation of microtubule arrays, ultimately predicting cell division orientation. Microtubules are destabilized under low tension, whereas stretching of cells, either through wounding or external aspiration, immediately induces their polymerization. The higher microtubule abundance in the stretched cell parts leads to the reorientation of microtubule arrays and, ultimately, informs cell division planes. This provides a long-sought mechanism for flexible re-arrangement of cell divisions by mechanical forces for tissue reconstruction and plant architecture.},
	number = {10},
	urldate = {2024-05-24},
	journal = {Developmental Cell},
	author = {Hoermayer, Lukas and Montesinos, Juan Carlos and Trozzi, Nicola and Spona, Leonhard and Yoshida, Saiko and Marhava, Petra and Caballero-Mancebo, Silvia and Benková, Eva and Heisenberg, Carl-Philip and Dagdas, Yasin and Majda, Mateusz and Friml, Jiří},
	month = may,
	year = {2024},
	keywords = {ablation, cell division, cell division plane, cell expansion, mechanical forces, microscopy, microtubules, plant development},
	pages = {1333--1344.e4},
}



Plant morphogenesis relies exclusively on oriented cell expansion and division. Nonetheless, the mechanism(s) determining division plane orientation remain elusive. Here, we studied tissue healing after laser-assisted wounding in roots of Arabidopsis thaliana and uncovered how mechanical forces stabilize and reorient the microtubule cytoskeleton for the orientation of cell division. We identified that root tissue functions as an interconnected cell matrix, with a radial gradient of tissue extendibility causing predictable tissue deformation after wounding. This deformation causes instant redirection of expansion in the surrounding cells and reorientation of microtubule arrays, ultimately predicting cell division orientation. Microtubules are destabilized under low tension, whereas stretching of cells, either through wounding or external aspiration, immediately induces their polymerization. The higher microtubule abundance in the stretched cell parts leads to the reorientation of microtubule arrays and, ultimately, informs cell division planes. This provides a long-sought mechanism for flexible re-arrangement of cell divisions by mechanical forces for tissue reconstruction and plant architecture.
  2023 (1)
Regulation of PIN polarity in response to abiotic stress. Sharma, M., & Marhava, P. Current Opinion in Plant Biology, 76: 102445. December 2023.
Regulation of PIN polarity in response to abiotic stress [link]Paper   doi   link   bibtex   abstract  
@article{sharma_regulation_2023,
	title = {Regulation of {PIN} polarity in response to abiotic stress},
	volume = {76},
	issn = {1369-5266},
	url = {https://www.sciencedirect.com/science/article/pii/S1369526623001103},
	doi = {10.1016/j.pbi.2023.102445},
	abstract = {Plants have evolved robust adaptive mechanisms to withstand the ever-changing environment. Tightly regulated distribution of the hormone auxin throughout the plant body controls an impressive variety of developmental processes that tailor plant growth and morphology to environmental conditions. The proper flow and directionality of auxin between cells is mainly governed by asymmetrically localized efflux carriers – PINs – ensuring proper coordination of developmental processes in plants. Discerning the molecular players and cellular dynamics involved in the establishment and maintenance of PINs in specific membrane domains, as well as their ability to readjust in response to abiotic stressors is essential for understanding how plants balance adaptability and stability. While much is known about how PINs get polarized, there is still limited knowledge about how abiotic stresses alter PIN polarity by acting on these systems. In this review, we focus on the current understanding of mechanisms involved in (re)establishing and maintaining PIN polarity under abiotic stresses.},
	urldate = {2023-12-22},
	journal = {Current Opinion in Plant Biology},
	author = {Sharma, Manvi and Marhava, Petra},
	month = dec,
	year = {2023},
	pages = {102445},
}



Plants have evolved robust adaptive mechanisms to withstand the ever-changing environment. Tightly regulated distribution of the hormone auxin throughout the plant body controls an impressive variety of developmental processes that tailor plant growth and morphology to environmental conditions. The proper flow and directionality of auxin between cells is mainly governed by asymmetrically localized efflux carriers – PINs – ensuring proper coordination of developmental processes in plants. Discerning the molecular players and cellular dynamics involved in the establishment and maintenance of PINs in specific membrane domains, as well as their ability to readjust in response to abiotic stressors is essential for understanding how plants balance adaptability and stability. While much is known about how PINs get polarized, there is still limited knowledge about how abiotic stresses alter PIN polarity by acting on these systems. In this review, we focus on the current understanding of mechanisms involved in (re)establishing and maintaining PIN polarity under abiotic stresses.
  2022 (1)
Recent developments in the understanding of PIN polarity. Marhava, P. New Phytologist, 233(2): 624–630. January 2022.
Recent developments in the understanding of PIN polarity [link]Paper   doi   link   bibtex   abstract   60 downloads  
@article{marhava_recent_2022,
	title = {Recent developments in the understanding of {PIN} polarity},
	volume = {233},
	issn = {1469-8137},
	url = {https://onlinelibrary.wiley.com/doi/abs/10.1111/nph.17867},
	doi = {10/gnr3sd},
	abstract = {Polar localization of PIN-FORMED proteins (PINs) at the plasma membrane is essential for plant development as they direct the transport of phytohormone auxin between cells. PIN polar localization to certain sides of a given cell is dynamic, strictly regulated and provides directionality to auxin flow. Signals that act upstream to control subcellular PIN localization modulate auxin distribution, thereby regulating diverse aspects of plant development. Here I summarize the current understanding of mechanisms by which PIN polarity is established, maintained and rearranged to provide a glimpse into the complexity of PIN polarity.},
	language = {en},
	number = {2},
	urldate = {2021-12-14},
	journal = {New Phytologist},
	author = {Marhava, Petra},
	month = jan,
	year = {2022},
	keywords = {PIN clustering, PIN polarity establishment, PIN polarity maintenance, auxin transport, self-reinforcing polarity},
	pages = {624--630},
}



Polar localization of PIN-FORMED proteins (PINs) at the plasma membrane is essential for plant development as they direct the transport of phytohormone auxin between cells. PIN polar localization to certain sides of a given cell is dynamic, strictly regulated and provides directionality to auxin flow. Signals that act upstream to control subcellular PIN localization modulate auxin distribution, thereby regulating diverse aspects of plant development. Here I summarize the current understanding of mechanisms by which PIN polarity is established, maintained and rearranged to provide a glimpse into the complexity of PIN polarity.
  2021 (1)
Mapping and engineering of auxin-induced plasma membrane dissociation in BRX family proteins. Koh, S. W H, Marhava, P., Rana, S., Graf, A., Moret, B., Bassukas, A. E L, Zourelidou, M., Kolb, M., Hammes, U. Z, Schwechheimer, C., & Hardtke, C. S The Plant Cell, 33(6): 1945–1960. June 2021.
Mapping and engineering of auxin-induced plasma membrane dissociation in BRX family proteins [link]Paper   doi   link   bibtex   abstract  
@article{koh_mapping_2021,
	title = {Mapping and engineering of auxin-induced plasma membrane dissociation in {BRX} family proteins},
	volume = {33},
	issn = {1040-4651},
	url = {https://doi.org/10.1093/plcell/koab076},
	doi = {10.1093/plcell/koab076},
	abstract = {Angiosperms have evolved the phloem for the long-distance transport of metabolites. The complex process of phloem development involves genes that only occur in vascular plant lineages. For example, in Arabidopsis thaliana, the BREVIS RADIX (BRX) gene is required for continuous root protophloem differentiation, together with PROTEIN KINASE ASSOCIATED WITH BRX (PAX). BRX and its BRX-LIKE (BRXL) homologs are composed of four highly conserved domains including the signature tandem BRX domains that are separated by variable spacers. Nevertheless, BRX family proteins have functionally diverged. For instance, BRXL2 can only partially replace BRX in the root protophloem. This divergence is reflected in physiologically relevant differences in protein behavior, such as auxin-induced plasma membrane dissociation of BRX, which is not observed for BRXL2. Here we dissected the differential functions of BRX family proteins using a set of amino acid substitutions and domain swaps. Our data suggest that the plasma membrane-associated tandem BRX domains are both necessary and sufficient to convey the biological outputs of BRX function and therefore constitute an important regulatory entity. Moreover, PAX target phosphosites in the linker between the two BRX domains mediate the auxin-induced plasma membrane dissociation. Engineering these sites into BRXL2 renders this modified protein auxin-responsive and thereby increases its biological activity in the root protophloem context.},
	number = {6},
	urldate = {2022-05-02},
	journal = {The Plant Cell},
	author = {Koh, Samuel W H and Marhava, Petra and Rana, Surbhi and Graf, Alina and Moret, Bernard and Bassukas, Alkistis E L and Zourelidou, Melina and Kolb, Martina and Hammes, Ulrich Z and Schwechheimer, Claus and Hardtke, Christian S},
	month = jun,
	year = {2021},
	pages = {1945--1960},
}



Angiosperms have evolved the phloem for the long-distance transport of metabolites. The complex process of phloem development involves genes that only occur in vascular plant lineages. For example, in Arabidopsis thaliana, the BREVIS RADIX (BRX) gene is required for continuous root protophloem differentiation, together with PROTEIN KINASE ASSOCIATED WITH BRX (PAX). BRX and its BRX-LIKE (BRXL) homologs are composed of four highly conserved domains including the signature tandem BRX domains that are separated by variable spacers. Nevertheless, BRX family proteins have functionally diverged. For instance, BRXL2 can only partially replace BRX in the root protophloem. This divergence is reflected in physiologically relevant differences in protein behavior, such as auxin-induced plasma membrane dissociation of BRX, which is not observed for BRXL2. Here we dissected the differential functions of BRX family proteins using a set of amino acid substitutions and domain swaps. Our data suggest that the plasma membrane-associated tandem BRX domains are both necessary and sufficient to convey the biological outputs of BRX function and therefore constitute an important regulatory entity. Moreover, PAX target phosphosites in the linker between the two BRX domains mediate the auxin-induced plasma membrane dissociation. Engineering these sites into BRXL2 renders this modified protein auxin-responsive and thereby increases its biological activity in the root protophloem context.
  2020 (5)
Arabidopsis Flippases Cooperate with ARF GTPase Exchange Factors to Regulate the Trafficking and Polarity of PIN Auxin Transporters[OPEN]. Zhang, X., Adamowski, M., Marhava, P., Tan, S., Zhang, Y., Rodriguez, L., Zwiewka, M., Pukyšová, V., Sánchez, A. S., Raxwal, V. K., Hardtke, C. S., Nodzyński, T., & Friml, J. The Plant Cell, 32(5): 1644–1664. May 2020.
Arabidopsis Flippases Cooperate with ARF GTPase Exchange Factors to Regulate the Trafficking and Polarity of PIN Auxin Transporters[OPEN] [link]Paper   doi   link   bibtex   abstract  
@article{zhang_arabidopsis_2020,
	title = {Arabidopsis {Flippases} {Cooperate} with {ARF} {GTPase} {Exchange} {Factors} to {Regulate} the {Trafficking} and {Polarity} of {PIN} {Auxin} {Transporters}[{OPEN}]},
	volume = {32},
	issn = {1040-4651},
	url = {https://doi.org/10.1105/tpc.19.00869},
	doi = {10.1105/tpc.19.00869},
	abstract = {Cell polarity is a fundamental feature of all multicellular organisms. PIN auxin transporters are important cell polarity markers that play crucial roles in a plethora of developmental processes in plants. Here, to identify components involved in cell polarity establishment and maintenance in plants, we performed a forward genetic screening of PIN2:PIN1-HA;pin2 Arabidopsis (Arabidopsis thaliana) plants, which ectopically express predominantly basally localized PIN1 in root epidermal cells, leading to agravitropic root growth. We identified the regulator of PIN polarity 12 (repp12) mutation, which restored gravitropic root growth and caused a switch in PIN1-HA polarity from the basal to apical side of root epidermal cells. Next Generation Sequencing and complementation experiments established the causative mutation of repp12 as a single amino acid exchange in Aminophospholipid ATPase3 (ALA3), a phospholipid flippase predicted to function in vesicle formation. repp12 and ala3 T-DNA mutants show defects in many auxin-regulated processes, asymmetric auxin distribution, and PIN trafficking. Analysis of quintuple and sextuple mutants confirmed the crucial roles of ALA proteins in regulating plant development as well as PIN trafficking and polarity. Genetic and physical interaction studies revealed that ALA3 functions together with the ADP ribosylation factor GTPase exchange factors GNOM and BIG3 in regulating PIN polarity, trafficking, and auxin-mediated development.},
	number = {5},
	urldate = {2022-05-02},
	journal = {The Plant Cell},
	author = {Zhang, Xixi and Adamowski, Maciek and Marhava, Petra and Tan, Shutang and Zhang, Yuzhou and Rodriguez, Lesia and Zwiewka, Marta and Pukyšová, Vendula and Sánchez, Adrià Sans and Raxwal, Vivek Kumar and Hardtke, Christian S. and Nodzyński, Tomasz and Friml, Jiří},
	month = may,
	year = {2020},
	pages = {1644--1664},
}



Cell polarity is a fundamental feature of all multicellular organisms. PIN auxin transporters are important cell polarity markers that play crucial roles in a plethora of developmental processes in plants. Here, to identify components involved in cell polarity establishment and maintenance in plants, we performed a forward genetic screening of PIN2:PIN1-HA;pin2 Arabidopsis (Arabidopsis thaliana) plants, which ectopically express predominantly basally localized PIN1 in root epidermal cells, leading to agravitropic root growth. We identified the regulator of PIN polarity 12 (repp12) mutation, which restored gravitropic root growth and caused a switch in PIN1-HA polarity from the basal to apical side of root epidermal cells. Next Generation Sequencing and complementation experiments established the causative mutation of repp12 as a single amino acid exchange in Aminophospholipid ATPase3 (ALA3), a phospholipid flippase predicted to function in vesicle formation. repp12 and ala3 T-DNA mutants show defects in many auxin-regulated processes, asymmetric auxin distribution, and PIN trafficking. Analysis of quintuple and sextuple mutants confirmed the crucial roles of ALA proteins in regulating plant development as well as PIN trafficking and polarity. Genetic and physical interaction studies revealed that ALA3 functions together with the ADP ribosylation factor GTPase exchange factors GNOM and BIG3 in regulating PIN polarity, trafficking, and auxin-mediated development.
Local and Systemic Effects of Brassinosteroid Perception in Developing Phloem. Graeff, M., Rana, S., Marhava, P., Moret, B., & Hardtke, C. S. Current Biology, 30(9): 1626–1638.e3. May 2020.
Local and Systemic Effects of Brassinosteroid Perception in Developing Phloem [link]Paper   doi   link   bibtex   abstract  
@article{graeff_local_2020,
	title = {Local and {Systemic} {Effects} of {Brassinosteroid} {Perception} in {Developing} {Phloem}},
	volume = {30},
	issn = {0960-9822},
	url = {https://www.sciencedirect.com/science/article/pii/S0960982220302025},
	doi = {10.1016/j.cub.2020.02.029},
	abstract = {The plant vasculature is an essential adaptation to terrestrial growth. Its phloem component permits efficient transfer of photosynthates between source and sink organs but also transports signals that systemically coordinate physiology and development. Here, we provide evidence that developing phloem orchestrates cellular behavior of adjacent tissues in the growth apices of plants, the meristems. Arabidopsis thaliana plants that lack the three receptor kinases BRASSINOSTEROID INSENSITIVE 1 (BRI1), BRI1-LIKE 1 (BRL1), and BRL3 (“bri3” mutants) can no longer sense brassinosteroid phytohormones and display severe dwarfism as well as patterning and differentiation defects, including disturbed phloem development. We found that, despite the ubiquitous expression of brassinosteroid receptors in growing plant tissues, exclusive expression of the BRI1 receptor in developing phloem is sufficient to systemically correct cellular growth and patterning defects that underlie the bri3 phenotype. Although this effect is brassinosteroid-dependent, it cannot be reproduced with dominant versions of known downstream effectors of BRI1 signaling and therefore possibly involves a non-canonical signaling output. Interestingly, the rescue of bri3 by phloem-specific BRI1 expression is associated with antagonism toward phloem-specific CLAVATA3/EMBRYO SURROUNDING REGION-RELATED 45 (CLE45) peptide signaling in roots. Hyperactive CLE45 signaling causes phloem sieve element differentiation defects, and consistently, knockout of CLE45 perception in bri3 background restores proper phloem development. However, bri3 dwarfism is retained in such lines. Our results thus reveal local and systemic effects of brassinosteroid perception in the phloem: whereas it locally antagonizes CLE45 signaling to permit phloem differentiation, it systemically instructs plant organ formation via a phloem-derived, non-cell-autonomous signal.},
	language = {en},
	number = {9},
	urldate = {2022-05-02},
	journal = {Current Biology},
	author = {Graeff, Moritz and Rana, Surbhi and Marhava, Petra and Moret, Bernard and Hardtke, Christian S.},
	month = may,
	year = {2020},
	keywords = {BAM3, BRI1, CLE45, brassinosteroids, organizer, phloem},
	pages = {1626--1638.e3},
}



The plant vasculature is an essential adaptation to terrestrial growth. Its phloem component permits efficient transfer of photosynthates between source and sink organs but also transports signals that systemically coordinate physiology and development. Here, we provide evidence that developing phloem orchestrates cellular behavior of adjacent tissues in the growth apices of plants, the meristems. Arabidopsis thaliana plants that lack the three receptor kinases BRASSINOSTEROID INSENSITIVE 1 (BRI1), BRI1-LIKE 1 (BRL1), and BRL3 (“bri3” mutants) can no longer sense brassinosteroid phytohormones and display severe dwarfism as well as patterning and differentiation defects, including disturbed phloem development. We found that, despite the ubiquitous expression of brassinosteroid receptors in growing plant tissues, exclusive expression of the BRI1 receptor in developing phloem is sufficient to systemically correct cellular growth and patterning defects that underlie the bri3 phenotype. Although this effect is brassinosteroid-dependent, it cannot be reproduced with dominant versions of known downstream effectors of BRI1 signaling and therefore possibly involves a non-canonical signaling output. Interestingly, the rescue of bri3 by phloem-specific BRI1 expression is associated with antagonism toward phloem-specific CLAVATA3/EMBRYO SURROUNDING REGION-RELATED 45 (CLE45) peptide signaling in roots. Hyperactive CLE45 signaling causes phloem sieve element differentiation defects, and consistently, knockout of CLE45 perception in bri3 background restores proper phloem development. However, bri3 dwarfism is retained in such lines. Our results thus reveal local and systemic effects of brassinosteroid perception in the phloem: whereas it locally antagonizes CLE45 signaling to permit phloem differentiation, it systemically instructs plant organ formation via a phloem-derived, non-cell-autonomous signal.
Local auxin competition explains fragmented differentiation patterns. Moret, B., Marhava, P., Aliaga Fandino, A. C., Hardtke, C. S., & ten Tusscher, K. H. W. Nature Communications, 11(1): 2965. June 2020. Number: 1 Publisher: Nature Publishing Group
Local auxin competition explains fragmented differentiation patterns [link]Paper   doi   link   bibtex   abstract  
@article{moret_local_2020,
	title = {Local auxin competition explains fragmented differentiation patterns},
	volume = {11},
	copyright = {2020 The Author(s)},
	issn = {2041-1723},
	url = {https://www.nature.com/articles/s41467-020-16803-7},
	doi = {10.1038/s41467-020-16803-7},
	abstract = {Trajectories of cellular ontogeny are tightly controlled and often involve feedback-regulated molecular antagonism. For example, sieve element differentiation along developing protophloem cell files of Arabidopsis roots requires two antagonistic regulators of auxin efflux. Paradoxically, loss-of-function in either regulator triggers similar, seemingly stochastic differentiation failures of individual sieve element precursors. Here we show that these patterning defects are distinct and non-random. They can be explained by auxin-dependent bistability that emerges from competition for auxin between neighboring cells. This bistability depends on the presence of an auxin influx facilitator, and can be triggered by either flux enhancement or repression. Our results uncover a hitherto overlooked aspect of auxin uptake, and highlight the contributions of local auxin influx, efflux and biosynthesis to protophloem formation. Moreover, the combined experimental-modeling approach suggests that without auxin efflux homeostasis, auxin influx interferes with coordinated differentiation.},
	language = {en},
	number = {1},
	urldate = {2022-05-02},
	journal = {Nature Communications},
	author = {Moret, Bernard and Marhava, Petra and Aliaga Fandino, Ana Cecilia and Hardtke, Christian S. and ten Tusscher, Kirsten H. W.},
	month = jun,
	year = {2020},
	note = {Number: 1
Publisher: Nature Publishing Group},
	keywords = {Auxin, Patterning},
	pages = {2965},
}



Trajectories of cellular ontogeny are tightly controlled and often involve feedback-regulated molecular antagonism. For example, sieve element differentiation along developing protophloem cell files of Arabidopsis roots requires two antagonistic regulators of auxin efflux. Paradoxically, loss-of-function in either regulator triggers similar, seemingly stochastic differentiation failures of individual sieve element precursors. Here we show that these patterning defects are distinct and non-random. They can be explained by auxin-dependent bistability that emerges from competition for auxin between neighboring cells. This bistability depends on the presence of an auxin influx facilitator, and can be triggered by either flux enhancement or repression. Our results uncover a hitherto overlooked aspect of auxin uptake, and highlight the contributions of local auxin influx, efflux and biosynthesis to protophloem formation. Moreover, the combined experimental-modeling approach suggests that without auxin efflux homeostasis, auxin influx interferes with coordinated differentiation.
Plasma Membrane Domain Patterning and Self-Reinforcing Polarity in Arabidopsis. Marhava, P., Aliaga Fandino, A. C., Koh, S. W. H., Jelínková, A., Kolb, M., Janacek, D. P., Breda, A. S., Cattaneo, P., Hammes, U. Z., Petrášek, J., & Hardtke, C. S. Developmental Cell, 52(2): 223–235.e5. January 2020.
Plasma Membrane Domain Patterning and Self-Reinforcing Polarity in Arabidopsis [link]Paper   doi   link   bibtex   abstract  
@article{marhava_plasma_2020,
	title = {Plasma {Membrane} {Domain} {Patterning} and {Self}-{Reinforcing} {Polarity} in {Arabidopsis}},
	volume = {52},
	issn = {1534-5807},
	url = {https://www.sciencedirect.com/science/article/pii/S1534580719309840},
	doi = {10.1016/j.devcel.2019.11.015},
	abstract = {Cell polarity is a key feature in the development of multicellular organisms. For instance, asymmetrically localized plasma-membrane-integral PIN-FORMED (PIN) proteins direct transcellular fluxes of the phytohormone auxin that govern plant development. Fine-tuned auxin flux is important for root protophloem sieve element differentiation and requires the interacting plasma-membrane-associated BREVIS RADIX (BRX) and PROTEIN KINASE ASSOCIATED WITH BRX (PAX) proteins. We observed “donut-like” polar PIN localization in developing sieve elements that depends on complementary, “muffin-like” polar localization of BRX and PAX. Plasma membrane association and polarity of PAX, and indirectly BRX, largely depends on phosphatidylinositol-4,5-bisphosphate. Consistently, mutants in phosphatidylinositol-4-phosphate 5-kinases (PIP5Ks) display protophloem differentiation defects similar to brx mutants. The same PIP5Ks are in complex with BRX and display “muffin-like” polar localization. Our data suggest that the BRX-PAX module recruits PIP5Ks to reinforce PAX polarity and thereby the polarity of all three proteins, which is required to maintain a local PIN minimum.},
	language = {en},
	number = {2},
	urldate = {2022-05-02},
	journal = {Developmental Cell},
	author = {Marhava, Petra and Aliaga Fandino, Ana Cecilia and Koh, Samuel W. H. and Jelínková, Adriana and Kolb, Martina and Janacek, Dorina P. and Breda, Alice S. and Cattaneo, Pietro and Hammes, Ulrich Z. and Petrášek, Jan and Hardtke, Christian S.},
	month = jan,
	year = {2020},
	keywords = {DRP1A, PIP5K1, PIP5K2, endocytosis, phloem, polar auxin transport, polarity, protophloem, root},
	pages = {223--235.e5},
}



Cell polarity is a key feature in the development of multicellular organisms. For instance, asymmetrically localized plasma-membrane-integral PIN-FORMED (PIN) proteins direct transcellular fluxes of the phytohormone auxin that govern plant development. Fine-tuned auxin flux is important for root protophloem sieve element differentiation and requires the interacting plasma-membrane-associated BREVIS RADIX (BRX) and PROTEIN KINASE ASSOCIATED WITH BRX (PAX) proteins. We observed “donut-like” polar PIN localization in developing sieve elements that depends on complementary, “muffin-like” polar localization of BRX and PAX. Plasma membrane association and polarity of PAX, and indirectly BRX, largely depends on phosphatidylinositol-4,5-bisphosphate. Consistently, mutants in phosphatidylinositol-4-phosphate 5-kinases (PIP5Ks) display protophloem differentiation defects similar to brx mutants. The same PIP5Ks are in complex with BRX and display “muffin-like” polar localization. Our data suggest that the BRX-PAX module recruits PIP5Ks to reinforce PAX polarity and thereby the polarity of all three proteins, which is required to maintain a local PIN minimum.
Wounding-induced changes in cellular pressure and localized auxin signalling spatially coordinate restorative divisions in roots. Hoermayer, L., Montesinos, J. C., Marhava, P., Benková, E., Yoshida, S., & Friml, J. Proceedings of the National Academy of Sciences, 117(26): 15322–15331. June 2020. Publisher: Proceedings of the National Academy of Sciences
Wounding-induced changes in cellular pressure and localized auxin signalling spatially coordinate restorative divisions in roots [link]Paper   doi   link   bibtex  
@article{hoermayer_wounding-induced_2020,
	title = {Wounding-induced changes in cellular pressure and localized auxin signalling spatially coordinate restorative divisions in roots},
	volume = {117},
	url = {https://www.pnas.org/doi/full/10.1073/pnas.2003346117},
	doi = {10.1073/pnas.2003346117},
	number = {26},
	urldate = {2022-05-16},
	journal = {Proceedings of the National Academy of Sciences},
	author = {Hoermayer, Lukas and Montesinos, Juan Carlos and Marhava, Petra and Benková, Eva and Yoshida, Saiko and Friml, Jiří},
	month = jun,
	year = {2020},
	note = {Publisher: Proceedings of the National Academy of Sciences},
	pages = {15322--15331},
}



  2019 (2)
Conditional effects of the epigenetic regulator JUMONJI 14 in Arabidopsis root growth. Cattaneo, P., Graeff, M., Marhava, P., & Hardtke, C. S. Development, 146(23): dev183905. December 2019.
Conditional effects of the epigenetic regulator JUMONJI 14 in Arabidopsis root growth [link]Paper   doi   link   bibtex   abstract  
@article{cattaneo_conditional_2019,
	title = {Conditional effects of the epigenetic regulator {JUMONJI} 14 in {Arabidopsis} root growth},
	volume = {146},
	issn = {0950-1991},
	url = {https://doi.org/10.1242/dev.183905},
	doi = {10.1242/dev.183905},
	abstract = {Methylation of lysine 4 in histone 3 (H3K4) is a post-translational modification that promotes gene expression. H3K4 methylation can be reversed by specific demethylases with an enzymatic Jumonji C domain. In Arabidopsis thaliana, H3K4-specific JUMONJI (JMJ) proteins distinguish themselves by the association with an F/Y-rich (FYR) domain. Here, we report that jmj14 mutations partially suppress reduced root meristem size and growth vigor of brevis radix (brx) mutants. Similar to its close homologs, JMJ15, JMJ16 and JMJ18, the JMJ14 promoter confers expression in mature root vasculature. Yet, unlike jmj14, neither jmj16 nor jmj18 mutation markedly suppresses brx phenotypes. Domain-swapping experiments suggest that the specificity of JMJ14 function resides in the FYR domain. Despite JMJ14 promoter activity in the mature vasculature, jmj14 mutation affects root meristem size. However, JMJ14 protein is observed throughout the meristem, suggesting that the JMJ14 transcript region contributes substantially to the spatial aspect of JMJ14 expression. In summary, our data reveal a role for JMJ14 in root growth in sensitized genetic backgrounds that depends on its FYR domain and regulatory input from the JMJ14 cistron.},
	number = {23},
	urldate = {2022-05-02},
	journal = {Development},
	author = {Cattaneo, Pietro and Graeff, Moritz and Marhava, Petra and Hardtke, Christian S.},
	month = dec,
	year = {2019},
	pages = {dev183905},
}



Methylation of lysine 4 in histone 3 (H3K4) is a post-translational modification that promotes gene expression. H3K4 methylation can be reversed by specific demethylases with an enzymatic Jumonji C domain. In Arabidopsis thaliana, H3K4-specific JUMONJI (JMJ) proteins distinguish themselves by the association with an F/Y-rich (FYR) domain. Here, we report that jmj14 mutations partially suppress reduced root meristem size and growth vigor of brevis radix (brx) mutants. Similar to its close homologs, JMJ15, JMJ16 and JMJ18, the JMJ14 promoter confers expression in mature root vasculature. Yet, unlike jmj14, neither jmj16 nor jmj18 mutation markedly suppresses brx phenotypes. Domain-swapping experiments suggest that the specificity of JMJ14 function resides in the FYR domain. Despite JMJ14 promoter activity in the mature vasculature, jmj14 mutation affects root meristem size. However, JMJ14 protein is observed throughout the meristem, suggesting that the JMJ14 transcript region contributes substantially to the spatial aspect of JMJ14 expression. In summary, our data reveal a role for JMJ14 in root growth in sensitized genetic backgrounds that depends on its FYR domain and regulatory input from the JMJ14 cistron.
Re-activation of Stem Cell Pathways for Pattern Restoration in Plant Wound Healing. Marhava, P., Hoermayer, L., Yoshida, S., Marhavý, P., Benková, E., & Friml, J. Cell, 177(4): 957–969.e13. May 2019.
Re-activation of Stem Cell Pathways for Pattern Restoration in Plant Wound Healing [link]Paper   doi   link   bibtex   4 downloads  
@article{marhava_re-activation_2019,
	title = {Re-activation of {Stem} {Cell} {Pathways} for {Pattern} {Restoration} in {Plant} {Wound} {Healing}},
	volume = {177},
	issn = {00928674},
	url = {https://linkinghub.elsevier.com/retrieve/pii/S0092867419304015},
	doi = {10/gfz9tc},
	language = {en},
	number = {4},
	urldate = {2021-06-07},
	journal = {Cell},
	author = {Marhava, Petra and Hoermayer, Lukas and Yoshida, Saiko and Marhavý, Peter and Benková, Eva and Friml, Jiří},
	month = may,
	year = {2019},
	pages = {957--969.e13},
}



  2018 (1)
A molecular rheostat adjusts auxin flux to promote root protophloem differentiation. Marhava, P., Bassukas, A. E. L., Zourelidou, M., Kolb, M., Moret, B., Fastner, A., Schulze, W. X., Cattaneo, P., Hammes, U. Z., Schwechheimer, C., & Hardtke, C. S. Nature, 558(7709): 297–300. June 2018. Number: 7709 Publisher: Nature Publishing Group
A molecular rheostat adjusts auxin flux to promote root protophloem differentiation [link]Paper   doi   link   bibtex   abstract  
@article{marhava_molecular_2018,
	title = {A molecular rheostat adjusts auxin flux to promote root protophloem differentiation},
	volume = {558},
	copyright = {2018 Macmillan Publishers Ltd., part of Springer Nature},
	issn = {1476-4687},
	url = {https://www.nature.com/articles/s41586-018-0186-z},
	doi = {10.1038/s41586-018-0186-z},
	abstract = {Auxin influences plant development through several distinct concentration-dependent effects1. In the Arabidopsis root tip, polar auxin transport by PIN-FORMED (PIN) proteins creates a local auxin accumulation that is required for the maintenance of the stem-cell niche2–4. Proximally, stem-cell daughter cells divide repeatedly before they eventually differentiate. This developmental gradient is accompanied by a gradual decrease in auxin levels as cells divide, and subsequently by a gradual increase as the cells differentiate5,6. However, the timing of differentiation is not uniform across cell files. For instance, developing protophloem sieve elements (PPSEs) differentiate as neighbouring cells still divide. Here we show that PPSE differentiation involves local steepening of the post-meristematic auxin gradient. BREVIS RADIX (BRX) and PROTEIN KINASE ASSOCIATED WITH BRX (PAX) are interacting plasma-membrane-associated, polarly localized proteins that co-localize with PIN proteins at the rootward end of developing PPSEs. Both brx and pax mutants display impaired PPSE differentiation. Similar to other AGC-family kinases, PAX activates PIN-mediated auxin efflux, whereas BRX strongly dampens this stimulation. Efficient BRX plasma-membrane localization depends on PAX, but auxin negatively regulates BRX plasma-membrane association and promotes PAX activity. Thus, our data support a model in which BRX and PAX are elements of a molecular rheostat that modulates auxin flux through developing PPSEs, thereby timing PPSE differentiation.},
	language = {en},
	number = {7709},
	urldate = {2022-05-02},
	journal = {Nature},
	author = {Marhava, P. and Bassukas, A. E. L. and Zourelidou, M. and Kolb, M. and Moret, B. and Fastner, A. and Schulze, W. X. and Cattaneo, P. and Hammes, U. Z. and Schwechheimer, C. and Hardtke, C. S.},
	month = jun,
	year = {2018},
	note = {Number: 7709
Publisher: Nature Publishing Group},
	keywords = {Auxin, Cell fate, Root apical meristem},
	pages = {297--300},
}



Auxin influences plant development through several distinct concentration-dependent effects1. In the Arabidopsis root tip, polar auxin transport by PIN-FORMED (PIN) proteins creates a local auxin accumulation that is required for the maintenance of the stem-cell niche2–4. Proximally, stem-cell daughter cells divide repeatedly before they eventually differentiate. This developmental gradient is accompanied by a gradual decrease in auxin levels as cells divide, and subsequently by a gradual increase as the cells differentiate5,6. However, the timing of differentiation is not uniform across cell files. For instance, developing protophloem sieve elements (PPSEs) differentiate as neighbouring cells still divide. Here we show that PPSE differentiation involves local steepening of the post-meristematic auxin gradient. BREVIS RADIX (BRX) and PROTEIN KINASE ASSOCIATED WITH BRX (PAX) are interacting plasma-membrane-associated, polarly localized proteins that co-localize with PIN proteins at the rootward end of developing PPSEs. Both brx and pax mutants display impaired PPSE differentiation. Similar to other AGC-family kinases, PAX activates PIN-mediated auxin efflux, whereas BRX strongly dampens this stimulation. Efficient BRX plasma-membrane localization depends on PAX, but auxin negatively regulates BRX plasma-membrane association and promotes PAX activity. Thus, our data support a model in which BRX and PAX are elements of a molecular rheostat that modulates auxin flux through developing PPSEs, thereby timing PPSE differentiation.
  2016 (1)
Targeted cell elimination reveals an auxin-guided biphasic mode of lateral root initiation. Marhavý, P., Montesinos, J. C., Abuzeineh, A., Van Damme, D., Vermeer, J. E., Duclercq, J., Rakusová, H., Nováková, P., Friml, J., Geldner, N., & Benková, E. Genes & Development, 30(4): 471–483. February 2016.
Targeted cell elimination reveals an auxin-guided biphasic mode of lateral root initiation [link]Paper   doi   link   bibtex   7 downloads  
@article{marhavy_targeted_2016,
	title = {Targeted cell elimination reveals an auxin-guided biphasic mode of lateral root initiation},
	volume = {30},
	issn = {0890-9369, 1549-5477},
	url = {http://genesdev.cshlp.org/lookup/doi/10.1101/gad.276964.115},
	doi = {10.1101/gad.276964.115},
	language = {en},
	number = {4},
	urldate = {2021-06-07},
	journal = {Genes \& Development},
	author = {Marhavý, Peter and Montesinos, Juan Carlos and Abuzeineh, Anas and Van Damme, Daniel and Vermeer, Joop E.M. and Duclercq, Jerôme and Rakusová, Hana and Nováková, Petra and Friml, Jiři and Geldner, Niko and Benková, Eva},
	month = feb,
	year = {2016},
	keywords = {auxin, lateral root organogenesis, mechanical forces, meristem proliferation activity},
	pages = {471--483},
}







  2015 (1)
Real-time Analysis of Lateral Root Organogenesis in Arabidopsis. Marhava, P., & Benkova, E. BIO-PROTOCOL, 5(8). 2015.
Real-time Analysis of Lateral Root Organogenesis in Arabidopsis [link]Paper   doi   link   bibtex  
@article{marhava_real-time_2015,
	title = {Real-time {Analysis} of {Lateral} {Root} {Organogenesis} in {Arabidopsis}},
	volume = {5},
	issn = {2331-8325},
	url = {http://www.bio-protocol.org/e1446},
	doi = {10/ggsz3x},
	language = {en},
	number = {8},
	urldate = {2021-06-07},
	journal = {BIO-PROTOCOL},
	author = {Marhava, Peter and Benkova, Eva},
	year = {2015},
}

  2014 (1)
SAC phosphoinositide phosphatases at the tonoplast mediate vacuolar function in Arabidopsis. Nováková, P., Hirsch, S., Feraru, E., Tejos, R., van Wijk, R., Viaene, T., Heilmann, M., Lerche, J., De Rycke, R., Feraru, M. I., Grones, P., Van Montagu, M., Heilmann, I., Munnik, T., & Friml, J. Proceedings of the National Academy of Sciences, 111(7): 2818–2823. February 2014. Publisher: Proceedings of the National Academy of Sciences
SAC phosphoinositide phosphatases at the tonoplast mediate vacuolar function in Arabidopsis [link]Paper   doi   link   bibtex   abstract  
@article{novakova_sac_2014,
	title = {{SAC} phosphoinositide phosphatases at the tonoplast mediate vacuolar function in {Arabidopsis}},
	volume = {111},
	url = {https://www.pnas.org/doi/10.1073/pnas.1324264111},
	doi = {10.1073/pnas.1324264111},
	abstract = {Phosphatidylinositol (PtdIns) is a structural phospholipid that can be phosphorylated into various lipid signaling molecules, designated polyphosphoinositides (PPIs). The reversible phosphorylation of PPIs on the 3, 4, or 5 position of inositol is performed by a set of organelle-specific kinases and phosphatases, and the characteristic head groups make these molecules ideal for regulating biological processes in time and space. In yeast and mammals, PtdIns3P and PtdIns(3,5)P2 play crucial roles in trafficking toward the lytic compartments, whereas the role in plants is not yet fully understood. Here we identified the role of a land plant-specific subgroup of PPI phosphatases, the suppressor of actin 2 (SAC2) to SAC5, during vacuolar trafficking and morphogenesis in Arabidopsis thaliana. SAC2–SAC5 localize to the tonoplast along with PtdIns3P, the presumable product of their activity. In SAC gain- and loss-of-function mutants, the levels of PtdIns monophosphates and bisphosphates were changed, with opposite effects on the morphology of storage and lytic vacuoles, and the trafficking toward the vacuoles was defective. Moreover, multiple sac knockout mutants had an increased number of smaller storage and lytic vacuoles, whereas extralarge vacuoles were observed in the overexpression lines, correlating with various growth and developmental defects. The fragmented vacuolar phenotype of sac mutants could be mimicked by treating wild-type seedlings with PtdIns(3,5)P2, corroborating that this PPI is important for vacuole morphology. Taken together, these results provide evidence that PPIs, together with their metabolic enzymes SAC2–SAC5, are crucial for vacuolar trafficking and for vacuolar morphology and function in plants.},
	number = {7},
	urldate = {2024-10-02},
	journal = {Proceedings of the National Academy of Sciences},
	author = {Nováková, Petra and Hirsch, Sibylle and Feraru, Elena and Tejos, Ricardo and van Wijk, Ringo and Viaene, Tom and Heilmann, Mareike and Lerche, Jennifer and De Rycke, Riet and Feraru, Mugurel I. and Grones, Peter and Van Montagu, Marc and Heilmann, Ingo and Munnik, Teun and Friml, Jiří},
	month = feb,
	year = {2014},
	note = {Publisher: Proceedings of the National Academy of Sciences},
	pages = {2818--2823},
}



Phosphatidylinositol (PtdIns) is a structural phospholipid that can be phosphorylated into various lipid signaling molecules, designated polyphosphoinositides (PPIs). The reversible phosphorylation of PPIs on the 3, 4, or 5 position of inositol is performed by a set of organelle-specific kinases and phosphatases, and the characteristic head groups make these molecules ideal for regulating biological processes in time and space. In yeast and mammals, PtdIns3P and PtdIns(3,5)P2 play crucial roles in trafficking toward the lytic compartments, whereas the role in plants is not yet fully understood. Here we identified the role of a land plant-specific subgroup of PPI phosphatases, the suppressor of actin 2 (SAC2) to SAC5, during vacuolar trafficking and morphogenesis in Arabidopsis thaliana. SAC2–SAC5 localize to the tonoplast along with PtdIns3P, the presumable product of their activity. In SAC gain- and loss-of-function mutants, the levels of PtdIns monophosphates and bisphosphates were changed, with opposite effects on the morphology of storage and lytic vacuoles, and the trafficking toward the vacuoles was defective. Moreover, multiple sac knockout mutants had an increased number of smaller storage and lytic vacuoles, whereas extralarge vacuoles were observed in the overexpression lines, correlating with various growth and developmental defects. The fragmented vacuolar phenotype of sac mutants could be mimicked by treating wild-type seedlings with PtdIns(3,5)P2, corroborating that this PPI is important for vacuole morphology. Taken together, these results provide evidence that PPIs, together with their metabolic enzymes SAC2–SAC5, are crucial for vacuolar trafficking and for vacuolar morphology and function in plants.
Torgeir Rhoden Hvidsten, Professor at the Norwegian University of Life Sciences

Hvidsten, Torgeir R. – Evolutionary analysis of gene regulatory networks

Research

Torgeir Rhoden Hvidsten, Professor at the Norwegian University of Life SciencesPhoto: Håkon Sparre/NMBU

In my research group, we use machine learning methods and large-scale genomics datasets to model how genes interact in regulatory networks, how regulatory networks evolve and how they give rise to complex properties characteristic to individuals and species.

Our main project aims to understand the process of wood formation in angiosperm and gymnosperm tree species by modelling the regulatory networks orchestrating the differentiation of stem cells into woody tissues. To this end, we are integrating large-scale multi-omics data to infer regulatory networks for several species and comparing these networks across species to identify regulatory mechanisms explaining the evolution of trees.

Network of different colored dots that are connected with lines Regulatory network of aspen wood formation

In another project, we work to understand how gene regulation evolves after whole genome duplication and to reveal to what degree these events, which play major roles in plant evolution, spark new regulatory innovations. To this end, we are developing phylogenetic methods for comparative analysis of omics data across multiple species.

In collaboration with Nathaniel Street, we are developing a number of online tools for facilitating comparative network analysis in plants. ComPlEx, available through the PlantGenIE portal (http://plantgenie.org), allows Comparative analysis of Plant Expression networks. AspWood (http://aspwood.popgenie.org) and NorWood (http://norwood.congenie.org) offer dedicated tools to analyze high-resolution gene expression data across wood formation in aspen and Norway spruce.

Read more about Torgeir Hvidsten's research here

Contact

Torgeir Rhoden Hvidsten, Professor at the Norwegian University of Life SciencesPhoto: Håkon Sparre/NMBU

Torgeir R. Hvidsten
Professor and BIAS group leader
Norwegian University of Life Sciences

Email: This email address is being protected from spambots. You need JavaScript enabled to view it.
Main homepage: http://www.trhvidsten.org/
Twitter: https://twitter.com/TRHvidsten


CV T. R. Hvidsten

Education

  • 2012: Docent, Umeå University (UmU), Umeå, Sweden
  • 2004: PhD, Linnaeus Centre for Bioinformatics, Uppsala University (UU), Sweden
  • 2000: MSc, Norwegian University of Science and Technology (NTNU), Norway

Positions

  • Since 2012: Professor, Norwegian University of Life Sciences (NMBU), Norway
  • 2012-2018: Guest professor, Umeå Plant Science Centre, Umeå University, Sweden
  • 2008-2012: Assistant professor, Umeå Plant Science Centre, Umeå University, Sweden
  • 2004-2008: Postdoc/Researcher, Linnaeus Centre for Bioinformatics, Uppsala University, Sweden

Publications

Please find a full list with publications from Torgeir Hvidsten here
 

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