Cargando…
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...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6490923/ https://www.ncbi.nlm.nih.gov/pubmed/30998684 http://dx.doi.org/10.1371/journal.pgen.1007847 |
_version_ | 1783414903743184896 |
---|---|
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_facet | 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 | Creff, Audrey |
collection | PubMed |
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. |
format | Online Article Text |
id | pubmed-6490923 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-64909232019-05-17 A stress-response-related inter-compartmental signalling pathway regulates embryonic cuticle integrity in Arabidopsis 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 PLoS Genet Research Article 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. Public Library of Science 2019-04-18 /pmc/articles/PMC6490923/ /pubmed/30998684 http://dx.doi.org/10.1371/journal.pgen.1007847 Text en © 2019 Creff et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article 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 A stress-response-related inter-compartmental signalling pathway regulates embryonic cuticle integrity in Arabidopsis |
title | A stress-response-related inter-compartmental signalling pathway regulates embryonic cuticle integrity in Arabidopsis |
title_full | A stress-response-related inter-compartmental signalling pathway regulates embryonic cuticle integrity in Arabidopsis |
title_fullStr | A stress-response-related inter-compartmental signalling pathway regulates embryonic cuticle integrity in Arabidopsis |
title_full_unstemmed | A stress-response-related inter-compartmental signalling pathway regulates embryonic cuticle integrity in Arabidopsis |
title_short | A stress-response-related inter-compartmental signalling pathway regulates embryonic cuticle integrity in Arabidopsis |
title_sort | stress-response-related inter-compartmental signalling pathway regulates embryonic cuticle integrity in arabidopsis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6490923/ https://www.ncbi.nlm.nih.gov/pubmed/30998684 http://dx.doi.org/10.1371/journal.pgen.1007847 |
work_keys_str_mv | AT creffaudrey astressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT brocardlysiane astressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT joubesjerome astressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT taconnatludivine astressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT dollnicolasm astressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT marsollierannecharlotte astressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT pascalstephanie astressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT gallettiroberta astressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT boeufsophy astressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT moussusteven astressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT widiezthomas astressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT domerguefrederic astressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT ingramgwyneth astressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT creffaudrey stressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT brocardlysiane stressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT joubesjerome stressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT taconnatludivine stressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT dollnicolasm stressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT marsollierannecharlotte stressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT pascalstephanie stressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT gallettiroberta stressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT boeufsophy stressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT moussusteven stressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT widiezthomas stressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT domerguefrederic stressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis AT ingramgwyneth stressresponserelatedintercompartmentalsignallingpathwayregulatesembryoniccuticleintegrityinarabidopsis |