Cargando…

ER-mediated control for abundance, quality, and signaling of transmembrane immune receptors in plants

Plants recognize a wide range of microbes with cell-surface and intracellular immune receptors. Transmembrane pattern recognition receptors (PRRs) initiate immune responses upon recognition of cognate ligands characteristic of microbes or aberrant cellular states, designated microbe-associated molec...

Descripción completa

Detalles Bibliográficos
Autores principales: Tintor, Nico, Saijo, Yusuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3933923/
https://www.ncbi.nlm.nih.gov/pubmed/24616730
http://dx.doi.org/10.3389/fpls.2014.00065
_version_ 1782305011209863168
author Tintor, Nico
Saijo, Yusuke
author_facet Tintor, Nico
Saijo, Yusuke
author_sort Tintor, Nico
collection PubMed
description Plants recognize a wide range of microbes with cell-surface and intracellular immune receptors. Transmembrane pattern recognition receptors (PRRs) initiate immune responses upon recognition of cognate ligands characteristic of microbes or aberrant cellular states, designated microbe-associated molecular patterns or danger-associated molecular patterns (DAMPs), respectively.Pattern-triggered immunity provides a first line of defense that restricts the invasion and propagation of both adapted and non-adapted pathogens. Receptor kinases (RKs) and receptor-like proteins (RLPs) with an extracellular leucine-rich repeat or lysine-motif (LysM) domain are extensively used as PRRs. The correct folding of the extracellular domain of these receptors is under quality control (QC) in the endoplasmic reticulum (ER), which thus provides a critical step in plant immunity. Genetic and structural insight suggests that ERQC regulates not only the abundance and quality of transmembrane receptors but also affects signal sorting between multi-branched pathways downstream of the receptor. However, ERQC dysfunction can also positively stimulate plant immunity, possibly through cell death and DAMP signaling pathways.
format Online
Article
Text
id pubmed-3933923
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-39339232014-03-10 ER-mediated control for abundance, quality, and signaling of transmembrane immune receptors in plants Tintor, Nico Saijo, Yusuke Front Plant Sci Plant Science Plants recognize a wide range of microbes with cell-surface and intracellular immune receptors. Transmembrane pattern recognition receptors (PRRs) initiate immune responses upon recognition of cognate ligands characteristic of microbes or aberrant cellular states, designated microbe-associated molecular patterns or danger-associated molecular patterns (DAMPs), respectively.Pattern-triggered immunity provides a first line of defense that restricts the invasion and propagation of both adapted and non-adapted pathogens. Receptor kinases (RKs) and receptor-like proteins (RLPs) with an extracellular leucine-rich repeat or lysine-motif (LysM) domain are extensively used as PRRs. The correct folding of the extracellular domain of these receptors is under quality control (QC) in the endoplasmic reticulum (ER), which thus provides a critical step in plant immunity. Genetic and structural insight suggests that ERQC regulates not only the abundance and quality of transmembrane receptors but also affects signal sorting between multi-branched pathways downstream of the receptor. However, ERQC dysfunction can also positively stimulate plant immunity, possibly through cell death and DAMP signaling pathways. Frontiers Media S.A. 2014-02-25 /pmc/articles/PMC3933923/ /pubmed/24616730 http://dx.doi.org/10.3389/fpls.2014.00065 Text en Copyright © 2014 Tintor and Saijo. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Tintor, Nico
Saijo, Yusuke
ER-mediated control for abundance, quality, and signaling of transmembrane immune receptors in plants
title ER-mediated control for abundance, quality, and signaling of transmembrane immune receptors in plants
title_full ER-mediated control for abundance, quality, and signaling of transmembrane immune receptors in plants
title_fullStr ER-mediated control for abundance, quality, and signaling of transmembrane immune receptors in plants
title_full_unstemmed ER-mediated control for abundance, quality, and signaling of transmembrane immune receptors in plants
title_short ER-mediated control for abundance, quality, and signaling of transmembrane immune receptors in plants
title_sort er-mediated control for abundance, quality, and signaling of transmembrane immune receptors in plants
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3933923/
https://www.ncbi.nlm.nih.gov/pubmed/24616730
http://dx.doi.org/10.3389/fpls.2014.00065
work_keys_str_mv AT tintornico ermediatedcontrolforabundancequalityandsignalingoftransmembraneimmunereceptorsinplants
AT saijoyusuke ermediatedcontrolforabundancequalityandsignalingoftransmembraneimmunereceptorsinplants