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Distinct guard cell specific remodeling of chromatin accessibility during abscisic acid and CO(2) dependent stomatal regulation
In plants, epidermal guard cells integrate and respond to numerous environmental signals to control stomatal pore apertures thereby regulating gas exchange. Chromatin structure controls transcription factor access to the genome, but whether large-scale chromatin remodeling occurs in guard cells duri...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197618/ https://www.ncbi.nlm.nih.gov/pubmed/37215031 http://dx.doi.org/10.1101/2023.05.11.540345 |
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author | Seller, Charles A. Schroeder, Julian I. |
author_facet | Seller, Charles A. Schroeder, Julian I. |
author_sort | Seller, Charles A. |
collection | PubMed |
description | In plants, epidermal guard cells integrate and respond to numerous environmental signals to control stomatal pore apertures thereby regulating gas exchange. Chromatin structure controls transcription factor access to the genome, but whether large-scale chromatin remodeling occurs in guard cells during stomatal movements, and in response to the hormone abscisic acid (ABA) in general, remain unknown. Here we isolate guard cell nuclei from Arabidopsis thaliana plants to examine whether the physiological signals, ABA and CO(2), regulate guard cell chromatin during stomatal movements. Our cell type specific analyses uncover patterns of chromatin accessibility specific to guard cells and define novel cis-regulatory sequences supporting guard cell specific gene expression. We find that ABA triggers extensive and dynamic chromatin remodeling in guard cells, roots, and mesophyll cells with clear patterns of cell-type specificity. DNA motif analyses uncover binding sites for distinct transcription factors enriched in ABA-induced and ABA-repressed chromatin. We identify the ABF/AREB bZIP-type transcription factors that are required for ABA-triggered chromatin opening in guard cells and implicate the inhibition of a set of bHLH-type transcription factors in controlling ABA-repressed chromatin. Moreover, we demonstrate that ABA and CO(2) induce distinct programs of chromatin remodeling. We provide insight into the control of guard cell chromatin dynamics and propose that ABA-induced chromatin remodeling primes the genome for abiotic stress resistance. |
format | Online Article Text |
id | pubmed-10197618 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-101976182023-05-20 Distinct guard cell specific remodeling of chromatin accessibility during abscisic acid and CO(2) dependent stomatal regulation Seller, Charles A. Schroeder, Julian I. bioRxiv Article In plants, epidermal guard cells integrate and respond to numerous environmental signals to control stomatal pore apertures thereby regulating gas exchange. Chromatin structure controls transcription factor access to the genome, but whether large-scale chromatin remodeling occurs in guard cells during stomatal movements, and in response to the hormone abscisic acid (ABA) in general, remain unknown. Here we isolate guard cell nuclei from Arabidopsis thaliana plants to examine whether the physiological signals, ABA and CO(2), regulate guard cell chromatin during stomatal movements. Our cell type specific analyses uncover patterns of chromatin accessibility specific to guard cells and define novel cis-regulatory sequences supporting guard cell specific gene expression. We find that ABA triggers extensive and dynamic chromatin remodeling in guard cells, roots, and mesophyll cells with clear patterns of cell-type specificity. DNA motif analyses uncover binding sites for distinct transcription factors enriched in ABA-induced and ABA-repressed chromatin. We identify the ABF/AREB bZIP-type transcription factors that are required for ABA-triggered chromatin opening in guard cells and implicate the inhibition of a set of bHLH-type transcription factors in controlling ABA-repressed chromatin. Moreover, we demonstrate that ABA and CO(2) induce distinct programs of chromatin remodeling. We provide insight into the control of guard cell chromatin dynamics and propose that ABA-induced chromatin remodeling primes the genome for abiotic stress resistance. Cold Spring Harbor Laboratory 2023-10-31 /pmc/articles/PMC10197618/ /pubmed/37215031 http://dx.doi.org/10.1101/2023.05.11.540345 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Seller, Charles A. Schroeder, Julian I. Distinct guard cell specific remodeling of chromatin accessibility during abscisic acid and CO(2) dependent stomatal regulation |
title | Distinct guard cell specific remodeling of chromatin accessibility during abscisic acid and CO(2) dependent stomatal regulation |
title_full | Distinct guard cell specific remodeling of chromatin accessibility during abscisic acid and CO(2) dependent stomatal regulation |
title_fullStr | Distinct guard cell specific remodeling of chromatin accessibility during abscisic acid and CO(2) dependent stomatal regulation |
title_full_unstemmed | Distinct guard cell specific remodeling of chromatin accessibility during abscisic acid and CO(2) dependent stomatal regulation |
title_short | Distinct guard cell specific remodeling of chromatin accessibility during abscisic acid and CO(2) dependent stomatal regulation |
title_sort | distinct guard cell specific remodeling of chromatin accessibility during abscisic acid and co(2) dependent stomatal regulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197618/ https://www.ncbi.nlm.nih.gov/pubmed/37215031 http://dx.doi.org/10.1101/2023.05.11.540345 |
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