Cargando…

Plant immune and growth receptors share common signalling components but localise to distinct plasma membrane nanodomains

Cell surface receptors govern a multitude of signalling pathways in multicellular organisms. In plants, prominent examples are the receptor kinases FLS2 and BRI1, which activate immunity and steroid-mediated growth, respectively. Intriguingly, despite inducing distinct signalling outputs, both recep...

Descripción completa

Detalles Bibliográficos
Autores principales: Bücherl, Christoph A, Jarsch, Iris K, Schudoma, Christian, Segonzac, Cécile, Mbengue, Malick, Robatzek, Silke, MacLean, Daniel, Ott, Thomas, Zipfel, Cyril
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5383397/
https://www.ncbi.nlm.nih.gov/pubmed/28262094
http://dx.doi.org/10.7554/eLife.25114
_version_ 1782520274373050368
author Bücherl, Christoph A
Jarsch, Iris K
Schudoma, Christian
Segonzac, Cécile
Mbengue, Malick
Robatzek, Silke
MacLean, Daniel
Ott, Thomas
Zipfel, Cyril
author_facet Bücherl, Christoph A
Jarsch, Iris K
Schudoma, Christian
Segonzac, Cécile
Mbengue, Malick
Robatzek, Silke
MacLean, Daniel
Ott, Thomas
Zipfel, Cyril
author_sort Bücherl, Christoph A
collection PubMed
description Cell surface receptors govern a multitude of signalling pathways in multicellular organisms. In plants, prominent examples are the receptor kinases FLS2 and BRI1, which activate immunity and steroid-mediated growth, respectively. Intriguingly, despite inducing distinct signalling outputs, both receptors employ common downstream signalling components, which exist in plasma membrane (PM)-localised protein complexes. An important question is thus how these receptor complexes maintain signalling specificity. Live-cell imaging revealed that FLS2 and BRI1 form PM nanoclusters. Using single-particle tracking we could discriminate both cluster populations and we observed spatiotemporal separation between immune and growth signalling platforms. This finding was confirmed by visualising FLS2 and BRI1 within distinct PM nanodomains marked by specific remorin proteins and differential co-localisation with the cytoskeleton. Our results thus suggest that signalling specificity between these pathways may be explained by the spatial separation of FLS2 and BRI1 with their associated signalling components within dedicated PM nanodomains. DOI: http://dx.doi.org/10.7554/eLife.25114.001
format Online
Article
Text
id pubmed-5383397
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-53833972017-04-10 Plant immune and growth receptors share common signalling components but localise to distinct plasma membrane nanodomains Bücherl, Christoph A Jarsch, Iris K Schudoma, Christian Segonzac, Cécile Mbengue, Malick Robatzek, Silke MacLean, Daniel Ott, Thomas Zipfel, Cyril eLife Cell Biology Cell surface receptors govern a multitude of signalling pathways in multicellular organisms. In plants, prominent examples are the receptor kinases FLS2 and BRI1, which activate immunity and steroid-mediated growth, respectively. Intriguingly, despite inducing distinct signalling outputs, both receptors employ common downstream signalling components, which exist in plasma membrane (PM)-localised protein complexes. An important question is thus how these receptor complexes maintain signalling specificity. Live-cell imaging revealed that FLS2 and BRI1 form PM nanoclusters. Using single-particle tracking we could discriminate both cluster populations and we observed spatiotemporal separation between immune and growth signalling platforms. This finding was confirmed by visualising FLS2 and BRI1 within distinct PM nanodomains marked by specific remorin proteins and differential co-localisation with the cytoskeleton. Our results thus suggest that signalling specificity between these pathways may be explained by the spatial separation of FLS2 and BRI1 with their associated signalling components within dedicated PM nanodomains. DOI: http://dx.doi.org/10.7554/eLife.25114.001 eLife Sciences Publications, Ltd 2017-03-06 /pmc/articles/PMC5383397/ /pubmed/28262094 http://dx.doi.org/10.7554/eLife.25114 Text en © 2017, Bücherl et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Bücherl, Christoph A
Jarsch, Iris K
Schudoma, Christian
Segonzac, Cécile
Mbengue, Malick
Robatzek, Silke
MacLean, Daniel
Ott, Thomas
Zipfel, Cyril
Plant immune and growth receptors share common signalling components but localise to distinct plasma membrane nanodomains
title Plant immune and growth receptors share common signalling components but localise to distinct plasma membrane nanodomains
title_full Plant immune and growth receptors share common signalling components but localise to distinct plasma membrane nanodomains
title_fullStr Plant immune and growth receptors share common signalling components but localise to distinct plasma membrane nanodomains
title_full_unstemmed Plant immune and growth receptors share common signalling components but localise to distinct plasma membrane nanodomains
title_short Plant immune and growth receptors share common signalling components but localise to distinct plasma membrane nanodomains
title_sort plant immune and growth receptors share common signalling components but localise to distinct plasma membrane nanodomains
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5383397/
https://www.ncbi.nlm.nih.gov/pubmed/28262094
http://dx.doi.org/10.7554/eLife.25114
work_keys_str_mv AT bucherlchristopha plantimmuneandgrowthreceptorssharecommonsignallingcomponentsbutlocalisetodistinctplasmamembranenanodomains
AT jarschirisk plantimmuneandgrowthreceptorssharecommonsignallingcomponentsbutlocalisetodistinctplasmamembranenanodomains
AT schudomachristian plantimmuneandgrowthreceptorssharecommonsignallingcomponentsbutlocalisetodistinctplasmamembranenanodomains
AT segonzaccecile plantimmuneandgrowthreceptorssharecommonsignallingcomponentsbutlocalisetodistinctplasmamembranenanodomains
AT mbenguemalick plantimmuneandgrowthreceptorssharecommonsignallingcomponentsbutlocalisetodistinctplasmamembranenanodomains
AT robatzeksilke plantimmuneandgrowthreceptorssharecommonsignallingcomponentsbutlocalisetodistinctplasmamembranenanodomains
AT macleandaniel plantimmuneandgrowthreceptorssharecommonsignallingcomponentsbutlocalisetodistinctplasmamembranenanodomains
AT ottthomas plantimmuneandgrowthreceptorssharecommonsignallingcomponentsbutlocalisetodistinctplasmamembranenanodomains
AT zipfelcyril plantimmuneandgrowthreceptorssharecommonsignallingcomponentsbutlocalisetodistinctplasmamembranenanodomains