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A RALF-brassinosteroid signaling circuit regulates Arabidopsis hypocotyl cell shape
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Abstract
Plant cells survey and modulate their cell walls to control their shape and anisotropic growth. Signaling mediated by the plant steroid hormones brassinosteroids (BR) plays a central role in coordinating cell wall status and cell growth, and alterations in the cell wall-BR feedback loop leads to life-threatening defects in tissue and cellular integrity. How the status of the cell wall is relayed to BR signaling remains largely unclear. Increasing evidence shows that RAPID ALKALANIZATION FACTORs (RALFs), a class of secreted peptides, play structural and signaling roles at the cell surface. Here, we show that loss of RALF signaling mediated by the plasma membrane-localized RALF receptor complex FERONIA (FER)-LORELEI-LIKE GPI-anchor protein 1 (LLG1) leads to defects in cell morphology, organization, and composition of the cell wall-including pectin methylation status-and to an increase in BR signaling. We observed that increase in BR signaling mitigates the cellular defects associated with the loss of FER-mediated RALF signaling. We show that perception of RALF23 promotes the formation and signaling activity of the main BR receptor complex formed by BRASSINOSTEROID INSENSITIVE 1 (BRI1) and BRI1-ASSOCIATED KINASE 1 (BAK1) and that its bioactivity relies on pectin status. Our observations suggest a model in which RALF peptides operate at the nexus between cell wall status and BR signaling, capable of inducing changes in the cell wall as well as functioning as a cell-wall-informed signaling cues initiating a feedback loop that solicits BR signaling and coordinates cell morphogenesis.
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Research works printed but not linked: 115
- Anderson, 2020, Dynamic Construction, Perception, and Remodeling of Plant Cell Walls, Annu. Rev. Plant Biol., 71, 39, 10.1146/annurev-arplant-081519-035846 · DOI
- Vaahtera, 2019, Cell wall integrity maintenance during plant development and interaction with the environment, Nat. Plants, 5, 924, 10.1038/s41477-019-0502-0 · DOI
- Hématy, 2007, A Receptor-like Kinase Mediates the Response of Arabidopsis Cells to the Inhibition of Cellulose Synthesis, Curr. Biol., 17, 922, 10.1016/j.cub.2007.05.018 · DOI
- Mecchia, 2017, RALF4/19 peptides interact with LRX proteins to control pollen tube growth in Arabidopsis, Science, 358, 1600, 10.1126/science.aao5467 · DOI
- Van der Does, 2017, The Arabidopsis leucine-rich repeat receptor kinase MIK2/LRR-KISS connects cell wall integrity sensing, root growth and response to abiotic and biotic stresses, PLOS Genet., 13, 10.1371/journal.pgen.1006832 · DOI
- Herger, 2019, Leucine-Rich Repeat Extensin Proteins and Their Role in Cell Wall Sensing, Curr. Biol., 29, R851, 10.1016/j.cub.2019.07.039 · DOI
- Chaudhary, 2020, The Arabidopsis receptor kinase STRUBBELIG regulates the response to cellulose deficiency, PLOS Genet., 16, 10.1371/journal.pgen.1008433 · DOI
- Wolf, 2022, Cell Wall Signaling in Plant Development and Defense, Annu. Rev. Plant Biol., 73, 323, 10.1146/annurev-arplant-102820-095312 · DOI
- Liu, 2023, FERONIA and wall-associated kinases coordinate defense induced by lignin modification in plant cell walls, Sci. Adv., 9
- Zhai, 2024, A peptide-receptor module links cell wall integrity sensing to pattern-triggered immunity, Nat. Plants, 10, 2027, 10.1038/s41477-024-01840-7 · DOI
- Srivastava, 2013, Quantitative Proteomics Reveals that Plasma Membrane Microdomains From Poplar Cell Suspension Cultures Are Enriched in Markers of Signal Transduction, Molecular Transport, and Callose Biosynthesis, Mol. Cell. Proteomics, 12, 3874, 10.1074/mcp.M113.029033 · DOI
- Gonneau, 2018, Receptor Kinase THESEUS1 Is a Rapid Alkalinization Factor 34 Receptor in Arabidopsis, Curr. Biol., 28, 2452, 10.1016/j.cub.2018.05.075 · DOI
- Dünser, 2019, Extracellular matrix sensing by FERONIA and Leucine-Rich Repeat Extensins controls vacuolar expansion during cellular elongation in Arabidopsis thaliana, EMBO J., 38, 10.15252/embj.2018100353 · DOI
- Li, 2018, EBP1 nuclear accumulation negatively feeds back on FERONIA-mediated RALF1 signaling, PLOS Biol., 16, 10.1371/journal.pbio.2006340 · DOI
- Gupta, 2024, Growth-inhibiting effects of the unconventional plant APYRASE 7 of Arabidopsis thaliana influences the LRX/RALF/FER growth regulatory module, PLOS Genet., 20, 10.1371/journal.pgen.1011087 · DOI
- Ge, 2017, Arabidopsis pollen tube integrity and sperm release are regulated by RALF-mediated signaling, Science, 358, 1596, 10.1126/science.aao3642 · DOI
- Zhong, 2022, RALF peptide signaling controls the polytubey block in Arabidopsis, Science, 375, 290, 10.1126/science.abl4683 · DOI
- Lan, 2023, Antagonistic RALF peptides control an intergeneric hybridization barrier on Brassicaceae stigmas, Cell, 186, 4773, 10.1016/j.cell.2023.09.003 · DOI
- Zhou, 2024, The RALF signaling pathway regulates cell wall integrity during pollen tube growth in maize, Plant Cell, 36, 1673, 10.1093/plcell/koad324 · DOI
- Feng, 2018, The FERONIA Receptor Kinase Maintains Cell-Wall Integrity during Salt Stress through Ca2+ Signaling, Curr. Biol., 28, 666, 10.1016/j.cub.2018.01.023 · DOI
- Zhao, 2018, Leucine-rich repeat extensin proteins regulate plant salt tolerance in Arabidopsis, Proc. Natl. Acad. Sci. USA, 115, 13123, 10.1073/pnas.1816991115 · DOI
- Zhao, 2021, The LRXs-RALFs-FER module controls plant growth and salt stress responses by modulating multiple plant hormones, Natl. Sci. Rev., 8, 10.1093/nsr/nwaa149 · DOI
- Stegmann, 2017, The receptor kinase FER is a RALF-regulated scaffold controlling plant immune signaling, Science, 355, 287, 10.1126/science.aal2541 · DOI
- Guo, 2018, FERONIA Receptor Kinase Contributes to Plant Immunity by Suppressing Jasmonic Acid Signaling in Arabidopsis thaliana, Curr. Biol., 28, 3316, 10.1016/j.cub.2018.07.078 · DOI
- Gronnier, 2022, Regulation of immune receptor kinase plasma membrane nanoscale organization by a plant peptide hormone and its receptors, eLife, 11, 10.7554/eLife.74162 · DOI
- Song, 2021, FERONIA restricts Pseudomonas in the rhizosphere microbiome via regulation of reactive oxygen species, Nat. Plants, 7, 644, 10.1038/s41477-021-00914-0 · DOI
- Tang, 2022, Plant immunity suppression via PHR1-RALF-FERONIA shapes the root microbiome to alleviate phosphate starvation, EMBO J., 41, 10.15252/embj.2021109102 · DOI
- Schoenaers, 2024, Rapid alkalinization factor 22 has a structural and signalling role in root hair cell wall assembly, Nat. Plants, 10, 494, 10.1038/s41477-024-01637-8 · DOI
- Moussu, 2023, Plant cell wall patterning and expansion mediated by protein-peptide-polysaccharide interaction, Science, 382, 719, 10.1126/science.adi4720 · DOI
- Moussu, 2020, Structural basis for recognition of RALF peptides by LRX proteins during pollen tube growth, Proc. Natl. Acad. Sci. USA, 117, 7494, 10.1073/pnas.2000100117 · DOI
- Liu, 2024, Extracellular pectin-RALF phase separation mediates FERONIA global signaling function, Cell, 187, 312, 10.1016/j.cell.2023.11.038 · DOI
- Rößling, 2024, Pectin methylesterase activity is required for RALF1 peptide signalling output, eLife, 13, 10.7554/eLife.96943 · DOI
- Herger, 2020, Overlapping functions and protein-protein interactions of LRR-extensins in Arabidopsis, PLOS Genet., 16, 10.1371/journal.pgen.1008847 · DOI
- Hedman, 2007, The source of Saturn’s G ring, Science, 317, 653, 10.1126/science.1143964 · DOI
- Haruta, 2014, A Peptide Hormone and Its Receptor Protein Kinase Regulate Plant Cell Expansion, Science, 343, 408, 10.1126/science.1244454 · DOI
- Capron, 2008, Maternal Control of Male-Gamete Delivery in Arabidopsis Involves a Putative GPI-Anchored Protein Encoded by the LORELEI Gene, Plant Cell, 20, 3038, 10.1105/tpc.108.061713 · DOI
- Li, 2015, Glycosylphosphatidylinositol-anchored proteins as chaperones and co-receptors for FERONIA receptor kinase signaling in Arabidopsis, eLife, 4, 10.7554/eLife.06587 · DOI
- Ge, 2019, LLG2/3 Are Co-receptors in BUPS/ANX-RALF Signaling to Regulate Arabidopsis Pollen Tube Integrity, Curr. Biol., 29, 3256, 10.1016/j.cub.2019.08.032 · DOI
- Xiao, 2019, Mechanisms of RALF peptide perception by a heterotypic receptor complex, Nature, 572, 270, 10.1038/s41586-019-1409-7 · DOI
- Pearce, 2001, RALF, a 5-kDa ubiquitous polypeptide in plants, arrests root growth and development, Proc. Natl. Acad. Sci. USA, 98, 12843, 10.1073/pnas.201416998 · DOI
- Morato do Canto, 2014, Biological activity of nine recombinant AtRALF peptides: Implications for their perception and function in Arabidopsis, Plant Physiol. Biochem., 75, 45, 10.1016/j.plaphy.2013.12.005 · DOI
- Li, 2022, RALF1 peptide triggers biphasic root growth inhibition upstream of auxin biosynthesis, Proc. Natl. Acad. Sci. USA, 119
- Abarca, 2021, Family-wide evaluation of RAPID ALKALINIZATION FACTOR peptides, Plant Physiol., 187, 996, 10.1093/plphys/kiab308 · DOI
- Gjetting, 2020, Evidence for multiple receptors mediating RALF-triggered Ca2+ signaling and proton pump inhibition, Plant J., 104, 433, 10.1111/tpj.14935 · DOI
- Gao, 2023, RALF signaling pathway activates MLO calcium channels to maintain pollen tube integrity, Cell Res., 33, 71, 10.1038/s41422-022-00754-3 · DOI
- Escobar-Restrepo, 2007, The FERONIA Receptor-like Kinase Mediates Male-Female Interactions During Pollen Tube Reception, Science, 317, 656, 10.1126/science.1143562 · DOI
- Yu, 2020, The RALF1-FERONIA interaction modulates endocytosis to mediate control of root growth in Arabidopsis, Development, 147
- Chen, 2023, CAR modulates plasma membrane nano-organization and immune signaling downstream of RALF1-FERONIA signaling pathway, New Phytol., 237, 2148, 10.1111/nph.18687 · DOI
- Smokvarska, 2023, The receptor kinase FERONIA regulates phosphatidylserine localization at the cell surface to modulate ROP signaling, Science Advances, 9, 10.1126/sciadv.add4791 · DOI
- Guo, 2018, FERONIA Receptor Kinase Contributes to Plant Immunity by Suppressing Jasmonic Acid Signaling in Arabidopsis thaliana, Curr. Biol., 28, 3316, 10.1016/j.cub.2018.07.078 · DOI
- Chen, 2024, Regulated cleavage and translocation of FERONIA control immunity in Arabidopsis roots, Nat. Plants, 10, 1761, 10.1038/s41477-024-01823-8 · DOI
- Li, 2002, BAK1, an Arabidopsis LRR Receptor-like Protein Kinase, Interacts with BRI1 and Modulates Brassinosteroid Signaling, Cell, 110, 213, 10.1016/S0092-8674(02)00812-7 · DOI
- Nam, 2002, BRI1/BAK1, a Receptor Kinase Pair Mediating Brassinosteroid Signaling, Cell, 110, 203, 10.1016/S0092-8674(02)00814-0 · DOI · Paper page
- Santiago, 2013, Molecular mechanism for plant steroid receptor activation by somatic embryogenesis co-receptor kinases, Science, 341, 889, 10.1126/science.1242468 · DOI · Paper page
- Ma, 2016, SERKing Coreceptors for Receptors, Trends Plant Sci., 21, 1017, 10.1016/j.tplants.2016.08.014 · DOI
- Wang, 2002, Nuclear-Localized BZR1 Mediates Brassinosteroid-Induced Growth and Feedback Suppression of Brassinosteroid Biosynthesis, Dev. Cell, 2, 505, 10.1016/S1534-5807(02)00153-3 · DOI
- Yin, 2002, BES1 Accumulates in the Nucleus in Response to Brassinosteroids to Regulate Gene Expression and Promote Stem Elongation, Cell, 109, 181, 10.1016/S0092-8674(02)00721-3 · DOI
- Kim, 2010, Brassinosteroid Signal Transduction from Receptor Kinases to Transcription Factors, Annu. Rev. Plant Biol., 61, 681, 10.1146/annurev.arplant.043008.092057 · DOI
- Belkhadir, 2015, The molecular circuitry of brassinosteroid signaling, New Phytol., 206, 522, 10.1111/nph.13269 · DOI
- Planas-Riverola, 2019, Brassinosteroid signaling in plant development and adaptation to stress, Development, 146, 10.1242/dev.151894 · DOI
- Nolan, 2023, Brassinosteroid gene regulatory networks at cellular resolution in the Arabidopsis root, Science, 379, 10.1126/science.adf4721 · DOI
- Wolf, 2012, Plant Cell Wall Homeostasis Is Mediated by Brassinosteroid Feedback Signaling, Curr. Biol., 22, 1732, 10.1016/j.cub.2012.07.036 · DOI
- Wolf, 2014, A receptor-like protein mediates the response to pectin modification by activating brassinosteroid signaling, Proc. Natl. Acad. Sci. USA, 111, 15261, 10.1073/pnas.1322979111 · DOI
- Sun, 2010, Integration of Brassinosteroid Signal Transduction with the Transcription Network for Plant Growth Regulation in Arabidopsis, Dev. Cell, 19, 765, 10.1016/j.devcel.2010.10.010 · DOI
- Yu, 2011, A brassinosteroid transcriptional network revealed by genome-wide identification of BESI target genes in Arabidopsis thaliana, Plant J., 65, 634, 10.1111/j.1365-313X.2010.04449.x · DOI
- Qu, 2011, Brassinosteroids regulate pectin methylesterase activity and AtPME41 expression in Arabidopsis under chilling stress, Cryobiology, 63, 111, 10.1016/j.cryobiol.2011.07.003 · DOI
- Xie, 2011, Brassinosteroids can regulate cellulose biosynthesis by controlling the expression of CESA genes in Arabidopsis, J. Exp. Bot., 62, 4495, 10.1093/jxb/err164 · DOI
- Sánchez-Rodríguez, 2017, BRASSINOSTEROID INSENSITIVE2 negatively regulates cellulose synthesis in Arabidopsis by phosphorylating cellulose synthase 1, Proc. Natl. Acad. Sci. USA, 114, 3533, 10.1073/pnas.1615005114 · DOI
- Kelly-Bellow, 2023, Brassinosteroid coordinates cell layer interactions in plants via cell wall and tissue mechanics, Science, 380, 1275, 10.1126/science.adf0752 · DOI
- Huerta, 2023, The WAK-like protein RFO1 acts as a sensor of the pectin methylation status in Arabidopsis cell walls to modulate root growth and defense, Mol. Plant, 16, 865, 10.1016/j.molp.2023.03.015 · DOI
- Yue, 2022, The receptor kinase OsWAK11 monitors cell wall pectin changes to fine-tune brassinosteroid signaling and regulate cell elongation in rice, Curr. Biol., 32, 2454, 10.1016/j.cub.2022.04.028 · DOI
- Deslauriers, 2010, FERONIA is a key modulator of brassinosteroid and ethylene responsiveness in arabidopsis hypocotyls, Mol. Plant, 3, 626, 10.1093/mp/ssq015 · DOI
- Duan, 2010, FERONIA receptor-like kinase regulates RHO GTPase signaling of root hair development, Proc. Natl. Acad. Sci. USA, 107, 17821, 10.1073/pnas.1005366107 · DOI
- Albrecht, 2012, Brassinosteroids inhibit pathogen-associated molecular pattern–triggered immune signaling independent of the receptor kinase BAK1, Proc. Natl. Acad. Sci. USA, 109, 303, 10.1073/pnas.1109921108 · DOI
- Shih, 2014, The receptor-like kinase FERONIA is required for mechanical signal transduction in Arabidopsis seedlings, Curr. Biol., 24, 1887, 10.1016/j.cub.2014.06.064 · DOI
- Malivert, 2021, FERONIA and microtubules independently contribute to mechanical integrity in the Arabidopsis shoot, PLOS Biol., 19, 10.1371/journal.pbio.3001454 · DOI
- Lin, 2022, Arabidopsis pavement cell morphogenesis requires FERONIA binding to pectin for activation of ROP GTPase signaling, Curr. Biol., 32, 497, 10.1016/j.cub.2021.11.030 · DOI
- Barbier de Reuille, 2015, MorphoGraphX: A platform for quantifying morphogenesis in 4D, eLife, 4, 10.7554/eLife.05864 · DOI
- Bidhendi, 2019, Mechanical Stress Initiates and Sustains the Morphogenesis of Wavy Leaf Epidermal Cells, Cell Rep., 28, 1237, 10.1016/j.celrep.2019.07.006 · DOI
- Majda, 2019, Mechanical Asymmetry of the Cell Wall Predicts Changes in Pavement Cell Geometry, Dev. Cell, 50, 9, 10.1016/j.devcel.2019.06.002 · DOI
- Cosgrove, 2020, Plant Cell Growth: Do Pectins Drive Lobe Formation in Arabidopsis Pavement Cells?, Curr. Biol., 30, R660, 10.1016/j.cub.2020.04.007 · DOI
- Haas, 2020, Pectin homogalacturonan nanofilament expansion drives morphogenesis in plant epidermal cells, Science, 367, 1003, 10.1126/science.aaz5103 · DOI
- Peaucelle, 2011, Pectin-Induced Changes in Cell Wall Mechanics Underlie Organ Initiation in Arabidopsis, Curr. Biol., 21, 1720, 10.1016/j.cub.2011.08.057 · DOI
- Peaucelle, 2015, The Control of Growth Symmetry Breaking in the Arabidopsis Hypocotyl, Curr. Biol., 25, 1746, 10.1016/j.cub.2015.05.022 · DOI
- Jonsson, 2021, Mechanochemical feedback mediates tissue bending required for seedling emergence, Curr. Biol., 31, 1154, 10.1016/j.cub.2020.12.016 · DOI
- Bou Daher, 2018, Anisotropic growth is achieved through the additive mechanical effect of material anisotropy and elastic asymmetry, eLife, 7, 10.7554/eLife.38161 · DOI
- Duan, 2020, FERONIA controls pectin- and nitric oxide-mediated male–female interaction, Nature, 579, 561, 10.1038/s41586-020-2106-2 · DOI
- Mravec, 2017, An oligogalacturonide-derived molecular probe demonstrates the dynamics of calcium-mediated pectin complexation in cell walls of tip-growing structures, Plant J., 91, 534, 10.1111/tpj.13574 · DOI
- Christiaens, 2011, Anti-homogalacturonan antibodies: A way to explore the effect of processing on pectin in fruits and vegetables?, Food Res. Int., 44, 225, 10.1016/j.foodres.2010.10.031 · DOI
- Pelloux, 2007, New insights into pectin methylesterase structure and function, Trends Plant Sci., 12, 267, 10.1016/j.tplants.2007.04.001 · DOI
- Lewis, 2008, Inhibition of pectin methyl esterase activity by green tea catechins, Phytochemistry, 69, 2586, 10.1016/j.phytochem.2008.08.012 · DOI
- Wang, 2012, Brassinosteroid Signaling Network and Regulation of Photomorphogenesis, Annu. Rev. Genet., 46, 701, 10.1146/annurev-genet-102209-163450 · DOI
- Fridman, 2013, Brassinosteroids in growth control: How, when and where, Plant Sci., 209, 24, 10.1016/j.plantsci.2013.04.002 · DOI
- Chinchilla, 2007, A flagellin-induced complex of the receptor FLS2 and BAK1 initiates plant defence, Nature, 448, 497, 10.1038/nature05999 · DOI
- Xu, 2008, Is kinase activity essential for biological functions of BRI1?, Cell Res., 18, 472, 10.1038/cr.2008.36 · DOI
- Tang, 2021, Mechano-transduction via the pectin-FERONIA complex activates ROP6 GTPase signaling in Arabidopsis pavement cell morphogenesis, Curr Biol, 32, 508, 10.1016/j.cub.2021.11.031 · DOI
- Boisson-Dernier, 2011, The walls have ears: the role of plant CrRLK1Ls in sensing and transducing extracellular signals, J. Exp. Bot., 62, 1581, 10.1093/jxb/erq445 · DOI
- Noble, 2022, Evolutionary analysis of the LORELEI gene family in plants reveals regulatory subfunctionalization, Plant Physiol., 190, 2539, 10.1093/plphys/kiac444 · DOI
- Caño-Delgado, 2004, BRL1 and BRL3 are novel brassinosteroid receptors that function in vascular differentiation in Arabidopsis, Development, 131, 5341, 10.1242/dev.01403 · DOI
- Chaudhary, 2025, FERONIA signaling maintains cell wall integrity during brassinosteroid-induced cell expansion in Arabidopsis, Mol. Plant, 18, 603, 10.1016/j.molp.2025.02.001 · DOI
- Perraki, 2018, Phosphocode-dependent functional dichotomy of a common co-receptor in plant signalling, Nature, 561, 248, 10.1038/s41586-018-0471-x · DOI
- Geldner, 2007, Endosomal signaling of plant steroid receptor kinase BRI1, Genes Dev., 21, 1598, 10.1101/gad.1561307 · DOI
- Schindelin, 2012, Fiji: an open-source platform for biological-image analysis, Nat. Methods, 9, 676, 10.1038/nmeth.2019 · DOI · Paper page
- Meng, 2023, UCSF ChimeraX: Tools for structure building and analysis, Protein Sci., 32, 10.1002/pro.4792 · DOI
- Kadota, 2014, Direct Regulation of the NADPH Oxidase RBOHD by the PRR-Associated Kinase BIK1 during Plant Immunity, Mol. Cell, 54, 43, 10.1016/j.molcel.2014.02.021 · DOI
- Roux, 2011, The Arabidopsis leucine-rich repeat receptor-like kinases BAK1/SERK3 and BKK1/SERK4 are required for innate immunity to hemibiotrophic and biotrophic pathogens, Plant Cell, 23, 2440, 10.1105/tpc.111.084301 · DOI
- Ursache, 2018, A protocol for combining fluorescent proteins with histological stains for diverse cell wall components, Plant J., 93, 399, 10.1111/tpj.13784 · DOI
- Preibisch, 2009, Globally optimal stitching of tiled 3D microscopic image acquisitions, Bioinformatics, 25, 1463, 10.1093/bioinformatics/btp184 · DOI · Paper page
- Gigli-Bisceglia, 2022, Arabidopsis root responses to salinity depend on pectin modification and cell wall sensing, Development, 149, 10.1242/dev.200363 · DOI
- Dubois, 1956, Colorimetric Method for Determination of Sugars and Related Substances, Anal. Chem., 28, 350, 10.1021/ac60111a017 · DOI · Paper page
- Nielsen, S.S. (2010) Phenol-Sulfuric Acid Method for Total Carbohydrates. 47–53. https://doi.org/10.1007/978-1-4419-1463-7_6. · DOI
- Bethke, 2014, Arabidopsis PECTIN METHYLESTERASEs Contribute to Immunity against Pseudomonas syringae, Plant Physiol., 164, 1093, 10.1104/pp.113.227637 · DOI
- Pettolino, 2012, Determining the polysaccharide composition of plant cell walls, Nat. Protoc., 7, 1590, 10.1038/nprot.2012.081 · DOI
- Yeats, 2016, Rapid Determination of Cellulose, Neutral Sugars, and Uronic Acids from Plant Cell Walls by One-step Two-step Hydrolysis and HPAEC-PAD, Bio Protoc., 6
- Lionetti, 2007, Overexpression of pectin methylesterase inhibitors in Arabidopsis restricts fungal infection by Botrytis cinerea, Plant Physiol., 143, 1871, 10.1104/pp.106.090803 · DOI
Metadata
- Authors
- Biermann, D., von Arx, M., Munzert-Eberlein, K. S., Xhelilaj, K., Séré, D., Stegmann, M., Vert, G., Wolf, S., Engelsdorf, T., Zipfel, C., & Gronnier, J.
- Affiliations
- Technical University of Munich (DE)
- University of Zurich (CH)
- University of Tübingen (DE)
- University of East Anglia (GB)
- Centre National de la Recherche Scientifique (FR)
- Philipps University of Marburg (DE)
- Corresponding author
- Zipfel, Cyril
- Gronnier, Julien
- ORCID
- Venue
- Current Biology
- Publisher
- Elsevier BV
- Published
- 2025-10
- Volume
- 35
- Issue
- 20
- Pages
- 5002-5017.e5
- ISSN
- 0960-9822 (ISSN-L)
- OpenAlex
- W4414573405
- Cited by
- 20
- References
- 3
- Citations by year
- 2026: 12 · 2025: 7
- FWCI
- 10.35
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Current Biology (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- HAL (submittedVersion, cc-by)
- Zurich Open Repository and Archive (University of Zurich) (submittedVersion, cc-by)
- Universitätsbibliothek Tübingen
- Funders
- European Research Council (309858, 773153)
- European Molecular Biology Organization (LTF 438-2018)
- University of Zurich
- German Research Foundation (B01-TRR356, A08-SFB1101, STE 2448/1)
- Gatsby Charitable Foundation
- Technical University of Munich
- Eberhard Karls Universität Tübingen
- Topics
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Polysaccharides and Plant Cell Walls
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Plant Reproductive Biology
- Keywords
- RALF peptides, brassinosteroid signaling, FERONIA, BRI1, BAK1, cell wall, pectin methylation, cell morphogenesis, Arabidopsis thaliana, plasma membrane signaling
- MeSH terms
- Cell Wall, Signal Transduction, Arabidopsis, Gene Expression Regulation, Plant, Hypocotyl, Arabidopsis Proteins, Cell Shape, Brassinosteroids
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