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A stress-response-related inter-compartmental signalling pathway regulates embryonic cuticle integrity in Arabidopsis
The embryonic cuticle is necessary for normal seed development and seedling establishment in Arabidopsis. Although mutants with defective embryonic cuticles have been identified, neither the deposition of cuticle material, nor its regulation, has been described during embryogenesis. Here we use elec...
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Published in: | PLoS genetics 2019-04, Vol.15 (4), p.e1007847-e1007847 |
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creator | Creff, Audrey Brocard, Lysiane Joubès, Jérôme Taconnat, Ludivine Doll, Nicolas M Marsollier, Anne-Charlotte Pascal, Stéphanie Galletti, Roberta Boeuf, Sophy Moussu, Steven Widiez, Thomas Domergue, Frédéric Ingram, Gwyneth |
description | The embryonic cuticle is necessary for normal seed development and seedling establishment in Arabidopsis. Although mutants with defective embryonic cuticles have been identified, neither the deposition of cuticle material, nor its regulation, has been described during embryogenesis. Here we use electron microscopy, cuticle staining and permeability assays to show that cuticle deposition initiates de novo in patches on globular embryos. By combining these techniques with genetics and gene expression analysis, we show that successful patch coalescence to form a continuous cuticle requires a signalling involving the endosperm-specific subtilisin protease ALE1 and the receptor kinases GSO1 and GSO2, which are expressed in the developing embryonic epidermis. Transcriptome analysis shows that this pathway regulates stress-related gene expression in seeds. Consistent with these findings we show genetically, and through activity analysis, that the stress-associated MPK6 protein acts downstream of GSO1 and GSO2 in the developing embryo. We propose that a stress-related signalling pathway has been hijacked in some angiosperm seeds through the recruitment of endosperm-specific components. Our work reveals the presence of an inter-compartmental dialogue between the endosperm and embryo that ensures the formation of an intact and functional cuticle around the developing embryo through an "auto-immune" type interaction. |
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Although mutants with defective embryonic cuticles have been identified, neither the deposition of cuticle material, nor its regulation, has been described during embryogenesis. Here we use electron microscopy, cuticle staining and permeability assays to show that cuticle deposition initiates de novo in patches on globular embryos. By combining these techniques with genetics and gene expression analysis, we show that successful patch coalescence to form a continuous cuticle requires a signalling involving the endosperm-specific subtilisin protease ALE1 and the receptor kinases GSO1 and GSO2, which are expressed in the developing embryonic epidermis. Transcriptome analysis shows that this pathway regulates stress-related gene expression in seeds. Consistent with these findings we show genetically, and through activity analysis, that the stress-associated MPK6 protein acts downstream of GSO1 and GSO2 in the developing embryo. We propose that a stress-related signalling pathway has been hijacked in some angiosperm seeds through the recruitment of endosperm-specific components. Our work reveals the presence of an inter-compartmental dialogue between the endosperm and embryo that ensures the formation of an intact and functional cuticle around the developing embryo through an "auto-immune" type interaction.</description><identifier>ISSN: 1553-7404</identifier><identifier>ISSN: 1553-7390</identifier><identifier>EISSN: 1553-7404</identifier><identifier>DOI: 10.1371/journal.pgen.1007847</identifier><identifier>PMID: 30998684</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Analysis ; Arabidopsis ; Arabidopsis - embryology ; Arabidopsis - physiology ; Arabidopsis Proteins - genetics ; Arabidopsis Proteins - metabolism ; Arabidopsis thaliana ; Biochemistry ; Cellular Biology ; Development Biology ; Electron microscopy ; Embryo ; Embryogenesis ; Embryonic development ; Embryonic Development - genetics ; Endosperm ; Endosperm - embryology ; Endosperm - genetics ; Epidermis ; Gene expression ; Gene Expression Regulation, Developmental ; Genetic aspects ; Humans ; Kinases ; Life Sciences ; Microscopy ; Mitogen-Activated Protein Kinases - genetics ; Mitogen-Activated Protein Kinases - metabolism ; Peptides ; Permeability ; Phenotype ; Physiological aspects ; Plant cuticle ; Plant Development - genetics ; Plants, Genetically Modified ; Proteases ; Seedlings ; Seeds ; Seeds - genetics ; Signal Transduction ; Signaling peptides and proteins ; Stress, Physiological - genetics ; Subtilisin ; Supervision ; Transgenes</subject><ispartof>PLoS genetics, 2019-04, Vol.15 (4), p.e1007847-e1007847</ispartof><rights>COPYRIGHT 2019 Public Library of Science</rights><rights>2019 Creff et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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Although mutants with defective embryonic cuticles have been identified, neither the deposition of cuticle material, nor its regulation, has been described during embryogenesis. Here we use electron microscopy, cuticle staining and permeability assays to show that cuticle deposition initiates de novo in patches on globular embryos. By combining these techniques with genetics and gene expression analysis, we show that successful patch coalescence to form a continuous cuticle requires a signalling involving the endosperm-specific subtilisin protease ALE1 and the receptor kinases GSO1 and GSO2, which are expressed in the developing embryonic epidermis. Transcriptome analysis shows that this pathway regulates stress-related gene expression in seeds. Consistent with these findings we show genetically, and through activity analysis, that the stress-associated MPK6 protein acts downstream of GSO1 and GSO2 in the developing embryo. We propose that a stress-related signalling pathway has been hijacked in some angiosperm seeds through the recruitment of endosperm-specific components. Our work reveals the presence of an inter-compartmental dialogue between the endosperm and embryo that ensures the formation of an intact and functional cuticle around the developing embryo through an "auto-immune" type interaction.</description><subject>Analysis</subject><subject>Arabidopsis</subject><subject>Arabidopsis - embryology</subject><subject>Arabidopsis - physiology</subject><subject>Arabidopsis Proteins - genetics</subject><subject>Arabidopsis Proteins - metabolism</subject><subject>Arabidopsis thaliana</subject><subject>Biochemistry</subject><subject>Cellular Biology</subject><subject>Development Biology</subject><subject>Electron microscopy</subject><subject>Embryo</subject><subject>Embryogenesis</subject><subject>Embryonic development</subject><subject>Embryonic Development - genetics</subject><subject>Endosperm</subject><subject>Endosperm - embryology</subject><subject>Endosperm - genetics</subject><subject>Epidermis</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Genetic aspects</subject><subject>Humans</subject><subject>Kinases</subject><subject>Life Sciences</subject><subject>Microscopy</subject><subject>Mitogen-Activated Protein Kinases - genetics</subject><subject>Mitogen-Activated Protein Kinases - metabolism</subject><subject>Peptides</subject><subject>Permeability</subject><subject>Phenotype</subject><subject>Physiological aspects</subject><subject>Plant cuticle</subject><subject>Plant Development - genetics</subject><subject>Plants, Genetically Modified</subject><subject>Proteases</subject><subject>Seedlings</subject><subject>Seeds</subject><subject>Seeds - genetics</subject><subject>Signal Transduction</subject><subject>Signaling peptides and proteins</subject><subject>Stress, Physiological - genetics</subject><subject>Subtilisin</subject><subject>Supervision</subject><subject>Transgenes</subject><issn>1553-7404</issn><issn>1553-7390</issn><issn>1553-7404</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqVk22L1DAQx4so3nn6DUQLgii4a9I8tW-E5VBvYfHAp7chTdJulrapSXq63970tndsj3uhFNIh-c1_MjOZJHkOwRIiBt_v7OA60Sz7WndLCADLMXuQnEJC0IJhgB8e2SfJE-93ACCSF-xxcoJAUeQ0x6fJsEp9cNr7RVx623kdjUYErVLTBe0W0ra9cKHVXRBN6k0dYzamq9NehO1vsU-drofRwae6Ld3edkamcghGNvpaonYm7KOVrpwojbK9N_5p8qgSjdfPpv9Z8uPTx-_nF4vN5ef1-WqzkIyisBBEV2WJWMaohHlZ6AxSgiDLUUloLnKFhAKoKrK8xJUSOc2EUpRWijApMdXoLHl50O0b6_lUMc-zjECAKaUoEusDoazY8d6ZVrg9t8Lw6w3rah6zH5PhRCgtUVUhJkpcwqokjFYMCQk1Uhkso9aHKdpQtlrJWDInmpno_KQzW17bK05xAYpsvMy7g8D2jtvFasNN7I1rOchiVzNErmDE30zxnP01aB94a7zUTSM6bYcxTQgLTCAelV_dQe8vxkTVIuZrusrGa8pRlK9IjrMii2uklvdQ8VO6NdJ2ujJxf-bwduYQmaD_hFoM3vP1t6__wX75d_by55x9fcRutWjC1tsmvtP45ucgPoDSWe-drm4bAQEfB--mcnwcPD4NXnR7cdz7W6ebSUN_AQDwKqw</recordid><startdate>20190418</startdate><enddate>20190418</enddate><creator>Creff, Audrey</creator><creator>Brocard, Lysiane</creator><creator>Joubès, Jérôme</creator><creator>Taconnat, Ludivine</creator><creator>Doll, Nicolas M</creator><creator>Marsollier, Anne-Charlotte</creator><creator>Pascal, Stéphanie</creator><creator>Galletti, Roberta</creator><creator>Boeuf, Sophy</creator><creator>Moussu, Steven</creator><creator>Widiez, Thomas</creator><creator>Domergue, Frédéric</creator><creator>Ingram, Gwyneth</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISN</scope><scope>ISR</scope><scope>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7SS</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-1425-9545</orcidid><orcidid>https://orcid.org/0000-0001-5385-450X</orcidid><orcidid>https://orcid.org/0000-0001-6002-2306</orcidid><orcidid>https://orcid.org/0000-0001-8299-7649</orcidid><orcidid>https://orcid.org/0000-0003-3277-4118</orcidid><orcidid>https://orcid.org/0000-0002-0183-7000</orcidid><orcidid>https://orcid.org/0000-0001-6710-3125</orcidid><orcidid>https://orcid.org/0000-0002-9956-6113</orcidid><orcidid>https://orcid.org/0000-0001-7912-7220</orcidid><orcidid>https://orcid.org/0000-0002-9397-1660</orcidid><orcidid>https://orcid.org/0000-0001-5429-8920</orcidid><orcidid>https://orcid.org/0000-0002-9600-8239</orcidid></search><sort><creationdate>20190418</creationdate><title>A stress-response-related inter-compartmental signalling pathway regulates embryonic cuticle integrity in Arabidopsis</title><author>Creff, Audrey ; Brocard, Lysiane ; Joubès, Jérôme ; Taconnat, Ludivine ; Doll, Nicolas M ; Marsollier, Anne-Charlotte ; Pascal, Stéphanie ; Galletti, Roberta ; Boeuf, Sophy ; Moussu, Steven ; Widiez, Thomas ; Domergue, Frédéric ; Ingram, Gwyneth</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c763t-a5efbb37276c18b9e216531783b568a8d3ad03f928b4fda862add66fd57cc46e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Analysis</topic><topic>Arabidopsis</topic><topic>Arabidopsis - 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Although mutants with defective embryonic cuticles have been identified, neither the deposition of cuticle material, nor its regulation, has been described during embryogenesis. Here we use electron microscopy, cuticle staining and permeability assays to show that cuticle deposition initiates de novo in patches on globular embryos. By combining these techniques with genetics and gene expression analysis, we show that successful patch coalescence to form a continuous cuticle requires a signalling involving the endosperm-specific subtilisin protease ALE1 and the receptor kinases GSO1 and GSO2, which are expressed in the developing embryonic epidermis. Transcriptome analysis shows that this pathway regulates stress-related gene expression in seeds. Consistent with these findings we show genetically, and through activity analysis, that the stress-associated MPK6 protein acts downstream of GSO1 and GSO2 in the developing embryo. We propose that a stress-related signalling pathway has been hijacked in some angiosperm seeds through the recruitment of endosperm-specific components. 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identifier | ISSN: 1553-7404 |
ispartof | PLoS genetics, 2019-04, Vol.15 (4), p.e1007847-e1007847 |
issn | 1553-7404 1553-7390 1553-7404 |
language | eng |
recordid | cdi_plos_journals_2251046663 |
source | Publicly Available Content Database (Proquest) (PQ_SDU_P3); PubMed Central Free |
subjects | Analysis Arabidopsis Arabidopsis - embryology Arabidopsis - physiology Arabidopsis Proteins - genetics Arabidopsis Proteins - metabolism Arabidopsis thaliana Biochemistry Cellular Biology Development Biology Electron microscopy Embryo Embryogenesis Embryonic development Embryonic Development - genetics Endosperm Endosperm - embryology Endosperm - genetics Epidermis Gene expression Gene Expression Regulation, Developmental Genetic aspects Humans Kinases Life Sciences Microscopy Mitogen-Activated Protein Kinases - genetics Mitogen-Activated Protein Kinases - metabolism Peptides Permeability Phenotype Physiological aspects Plant cuticle Plant Development - genetics Plants, Genetically Modified Proteases Seedlings Seeds Seeds - genetics Signal Transduction Signaling peptides and proteins Stress, Physiological - genetics Subtilisin Supervision Transgenes |
title | A stress-response-related inter-compartmental signalling pathway regulates embryonic cuticle integrity in Arabidopsis |
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