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Integrative analysis of the nuclear proteome in Pinus radiata reveals thermopriming coupled to epigenetic regulation

Despite it being an important issue in the context of climate change, for most plant species it is not currently known how abiotic stresses affect nuclear proteomes and mediate memory effects. This study examines how Pinus radiata nuclei respond, adapt, ‘remember’, and ‘learn’ from heat stress. Seed...

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Autores principales: Lamelas, Laura, Valledor, Luis, Escandón, Mónica, Pinto, Gloria, Cañal, María Jesús, Meijón, Mónica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094079/
https://www.ncbi.nlm.nih.gov/pubmed/31781741
http://dx.doi.org/10.1093/jxb/erz524
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author Lamelas, Laura
Valledor, Luis
Escandón, Mónica
Pinto, Gloria
Cañal, María Jesús
Meijón, Mónica
author_facet Lamelas, Laura
Valledor, Luis
Escandón, Mónica
Pinto, Gloria
Cañal, María Jesús
Meijón, Mónica
author_sort Lamelas, Laura
collection PubMed
description Despite it being an important issue in the context of climate change, for most plant species it is not currently known how abiotic stresses affect nuclear proteomes and mediate memory effects. This study examines how Pinus radiata nuclei respond, adapt, ‘remember’, and ‘learn’ from heat stress. Seedlings were heat-stressed at 45 °C for 10 d and then allowed to recover. Nuclear proteins were isolated and quantified by nLC-MS/MS, the dynamics of tissue DNA methylation were examined, and the potential acquired memory was analysed in recovered plants. In an additional experiment, the expression of key gene genes was also quantified. Specific nuclear heat-responsive proteins were identified, and their biological roles were evaluated using a systems biology approach. In addition to heat-shock proteins, several clusters involved in regulation processes were discovered, such as epigenomic-driven gene regulation, some transcription factors, and a variety of RNA-associated functions. Nuclei exhibited differential proteome profiles across the phases of the experiment, with histone H2A and methyl cycle enzymes in particular being accumulated in the recovery step. A thermopriming effect was possibly linked to H2A abundance and over-accumulation of spliceosome elements in recovered P. radiata plants. The results suggest that epigenetic mechanisms play a key role in heat-stress tolerance and priming mechanisms.
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spelling pubmed-70940792020-03-30 Integrative analysis of the nuclear proteome in Pinus radiata reveals thermopriming coupled to epigenetic regulation Lamelas, Laura Valledor, Luis Escandón, Mónica Pinto, Gloria Cañal, María Jesús Meijón, Mónica J Exp Bot Research Papers Despite it being an important issue in the context of climate change, for most plant species it is not currently known how abiotic stresses affect nuclear proteomes and mediate memory effects. This study examines how Pinus radiata nuclei respond, adapt, ‘remember’, and ‘learn’ from heat stress. Seedlings were heat-stressed at 45 °C for 10 d and then allowed to recover. Nuclear proteins were isolated and quantified by nLC-MS/MS, the dynamics of tissue DNA methylation were examined, and the potential acquired memory was analysed in recovered plants. In an additional experiment, the expression of key gene genes was also quantified. Specific nuclear heat-responsive proteins were identified, and their biological roles were evaluated using a systems biology approach. In addition to heat-shock proteins, several clusters involved in regulation processes were discovered, such as epigenomic-driven gene regulation, some transcription factors, and a variety of RNA-associated functions. Nuclei exhibited differential proteome profiles across the phases of the experiment, with histone H2A and methyl cycle enzymes in particular being accumulated in the recovery step. A thermopriming effect was possibly linked to H2A abundance and over-accumulation of spliceosome elements in recovered P. radiata plants. The results suggest that epigenetic mechanisms play a key role in heat-stress tolerance and priming mechanisms. Oxford University Press 2020-03-25 2019-11-29 /pmc/articles/PMC7094079/ /pubmed/31781741 http://dx.doi.org/10.1093/jxb/erz524 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Experimental Biology. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Papers
Lamelas, Laura
Valledor, Luis
Escandón, Mónica
Pinto, Gloria
Cañal, María Jesús
Meijón, Mónica
Integrative analysis of the nuclear proteome in Pinus radiata reveals thermopriming coupled to epigenetic regulation
title Integrative analysis of the nuclear proteome in Pinus radiata reveals thermopriming coupled to epigenetic regulation
title_full Integrative analysis of the nuclear proteome in Pinus radiata reveals thermopriming coupled to epigenetic regulation
title_fullStr Integrative analysis of the nuclear proteome in Pinus radiata reveals thermopriming coupled to epigenetic regulation
title_full_unstemmed Integrative analysis of the nuclear proteome in Pinus radiata reveals thermopriming coupled to epigenetic regulation
title_short Integrative analysis of the nuclear proteome in Pinus radiata reveals thermopriming coupled to epigenetic regulation
title_sort integrative analysis of the nuclear proteome in pinus radiata reveals thermopriming coupled to epigenetic regulation
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094079/
https://www.ncbi.nlm.nih.gov/pubmed/31781741
http://dx.doi.org/10.1093/jxb/erz524
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