Cargando…

Physiological and Proteomic Changes in the Apoplast Accompany Leaf Senescence in Arabidopsis

The apoplast, i.e. the cellular compartment external to the plasma membrane, undergoes important changes during senescence. Apoplastic fluid volume increases quite significantly in senescing leaves, thereby diluting its contents. Its pH elevates by about 0.8 units, similar to the apoplast alkalizati...

Descripción completa

Detalles Bibliográficos
Autores principales: Borniego, Maria L., Molina, Maria C., Guiamét, Juan J., Martinez, Dana E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6960232/
https://www.ncbi.nlm.nih.gov/pubmed/31969890
http://dx.doi.org/10.3389/fpls.2019.01635
_version_ 1783487748946001920
author Borniego, Maria L.
Molina, Maria C.
Guiamét, Juan J.
Martinez, Dana E.
author_facet Borniego, Maria L.
Molina, Maria C.
Guiamét, Juan J.
Martinez, Dana E.
author_sort Borniego, Maria L.
collection PubMed
description The apoplast, i.e. the cellular compartment external to the plasma membrane, undergoes important changes during senescence. Apoplastic fluid volume increases quite significantly in senescing leaves, thereby diluting its contents. Its pH elevates by about 0.8 units, similar to the apoplast alkalization in response to abiotic stresses. The levels of 159 proteins decrease, whereas 24 proteins increase in relative abundance in the apoplast of senescing leaves. Around half of the apoplastic proteins of non-senescent leaves contain a N-terminal signal peptide for secretion, while all the identified senescence-associated apoplastic proteins contain the signal peptide. Several of the apoplastic proteins that accumulate during senescence also accumulate in stress responses, suggesting that the apoplast may constitute a compartment where developmental and stress-related programs overlap. Other senescence-related apoplastic proteins are involved in cell wall modifications, proteolysis, carbohydrate, ROS and amino acid metabolism, signaling, lipid transport, etc. The most abundant senescence-associated apoplastic proteins, PR2 and PR5 (e.g. pathogenesis related proteins PR2 and PR5) are related to leaf aging rather than to the chloroplast degradation program, as their levels increase only in leaves undergoing developmental senescence, but not in dark-induced senescent leaves. Changes in the apoplastic space may be relevant for signaling and molecular trafficking underlying senescence.
format Online
Article
Text
id pubmed-6960232
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-69602322020-01-22 Physiological and Proteomic Changes in the Apoplast Accompany Leaf Senescence in Arabidopsis Borniego, Maria L. Molina, Maria C. Guiamét, Juan J. Martinez, Dana E. Front Plant Sci Plant Science The apoplast, i.e. the cellular compartment external to the plasma membrane, undergoes important changes during senescence. Apoplastic fluid volume increases quite significantly in senescing leaves, thereby diluting its contents. Its pH elevates by about 0.8 units, similar to the apoplast alkalization in response to abiotic stresses. The levels of 159 proteins decrease, whereas 24 proteins increase in relative abundance in the apoplast of senescing leaves. Around half of the apoplastic proteins of non-senescent leaves contain a N-terminal signal peptide for secretion, while all the identified senescence-associated apoplastic proteins contain the signal peptide. Several of the apoplastic proteins that accumulate during senescence also accumulate in stress responses, suggesting that the apoplast may constitute a compartment where developmental and stress-related programs overlap. Other senescence-related apoplastic proteins are involved in cell wall modifications, proteolysis, carbohydrate, ROS and amino acid metabolism, signaling, lipid transport, etc. The most abundant senescence-associated apoplastic proteins, PR2 and PR5 (e.g. pathogenesis related proteins PR2 and PR5) are related to leaf aging rather than to the chloroplast degradation program, as their levels increase only in leaves undergoing developmental senescence, but not in dark-induced senescent leaves. Changes in the apoplastic space may be relevant for signaling and molecular trafficking underlying senescence. Frontiers Media S.A. 2020-01-08 /pmc/articles/PMC6960232/ /pubmed/31969890 http://dx.doi.org/10.3389/fpls.2019.01635 Text en Copyright © 2020 Borniego, Molina, Guiamét and Martinez http://creativecommons.org/licenses/by/4.0/ 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) and the copyright owner(s) 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
Borniego, Maria L.
Molina, Maria C.
Guiamét, Juan J.
Martinez, Dana E.
Physiological and Proteomic Changes in the Apoplast Accompany Leaf Senescence in Arabidopsis
title Physiological and Proteomic Changes in the Apoplast Accompany Leaf Senescence in Arabidopsis
title_full Physiological and Proteomic Changes in the Apoplast Accompany Leaf Senescence in Arabidopsis
title_fullStr Physiological and Proteomic Changes in the Apoplast Accompany Leaf Senescence in Arabidopsis
title_full_unstemmed Physiological and Proteomic Changes in the Apoplast Accompany Leaf Senescence in Arabidopsis
title_short Physiological and Proteomic Changes in the Apoplast Accompany Leaf Senescence in Arabidopsis
title_sort physiological and proteomic changes in the apoplast accompany leaf senescence in arabidopsis
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6960232/
https://www.ncbi.nlm.nih.gov/pubmed/31969890
http://dx.doi.org/10.3389/fpls.2019.01635
work_keys_str_mv AT borniegomarial physiologicalandproteomicchangesintheapoplastaccompanyleafsenescenceinarabidopsis
AT molinamariac physiologicalandproteomicchangesintheapoplastaccompanyleafsenescenceinarabidopsis
AT guiametjuanj physiologicalandproteomicchangesintheapoplastaccompanyleafsenescenceinarabidopsis
AT martinezdanae physiologicalandproteomicchangesintheapoplastaccompanyleafsenescenceinarabidopsis