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Dynamic Deposition of Histone Variant H3.3 Accompanies Developmental Remodeling of the Arabidopsis Transcriptome

In animals, replication-coupled histone H3.1 can be distinguished from replication-independent histone H3.3. H3.3 variants are enriched at active genes and their promoters. Furthermore, H3.3 is specifically incorporated upon gene activation. Histone H3 variants evolved independently in plants and an...

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Autores principales: Wollmann, Heike, Holec, Sarah, Alden, Keith, Clarke, Neil D., Jacques, Pierre-Étienne, Berger, Frédéric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342937/
https://www.ncbi.nlm.nih.gov/pubmed/22570629
http://dx.doi.org/10.1371/journal.pgen.1002658
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author Wollmann, Heike
Holec, Sarah
Alden, Keith
Clarke, Neil D.
Jacques, Pierre-Étienne
Berger, Frédéric
author_facet Wollmann, Heike
Holec, Sarah
Alden, Keith
Clarke, Neil D.
Jacques, Pierre-Étienne
Berger, Frédéric
author_sort Wollmann, Heike
collection PubMed
description In animals, replication-coupled histone H3.1 can be distinguished from replication-independent histone H3.3. H3.3 variants are enriched at active genes and their promoters. Furthermore, H3.3 is specifically incorporated upon gene activation. Histone H3 variants evolved independently in plants and animals, and it is unclear whether different replication-independent H3.3 variants developed similar properties in both phyla. We studied Arabidopsis H3 variants in order to find core properties of this class of histones. Here we present genome-wide maps of H3.3 and H3.1 enrichment and the dynamic changes of their profiles upon cell division arrest. We find H3.3 enrichment to positively correlate with gene expression and to be biased towards the transcription termination site. In contrast with H3.1, heterochromatic regions are mostly depleted of H3.3. We report that, in planta, dynamic changes in H3.3 profiles are associated with the extensive remodeling of the transcriptome that occurs during cell differentiation. We propose that H3.3 dynamics are linked to transcription and are involved in resetting covalent histone marks at a genomic scale during plant development. Our study suggests that H3 variants properties likely result from functionally convergent evolution.
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spelling pubmed-33429372012-05-08 Dynamic Deposition of Histone Variant H3.3 Accompanies Developmental Remodeling of the Arabidopsis Transcriptome Wollmann, Heike Holec, Sarah Alden, Keith Clarke, Neil D. Jacques, Pierre-Étienne Berger, Frédéric PLoS Genet Research Article In animals, replication-coupled histone H3.1 can be distinguished from replication-independent histone H3.3. H3.3 variants are enriched at active genes and their promoters. Furthermore, H3.3 is specifically incorporated upon gene activation. Histone H3 variants evolved independently in plants and animals, and it is unclear whether different replication-independent H3.3 variants developed similar properties in both phyla. We studied Arabidopsis H3 variants in order to find core properties of this class of histones. Here we present genome-wide maps of H3.3 and H3.1 enrichment and the dynamic changes of their profiles upon cell division arrest. We find H3.3 enrichment to positively correlate with gene expression and to be biased towards the transcription termination site. In contrast with H3.1, heterochromatic regions are mostly depleted of H3.3. We report that, in planta, dynamic changes in H3.3 profiles are associated with the extensive remodeling of the transcriptome that occurs during cell differentiation. We propose that H3.3 dynamics are linked to transcription and are involved in resetting covalent histone marks at a genomic scale during plant development. Our study suggests that H3 variants properties likely result from functionally convergent evolution. Public Library of Science 2012-05-03 /pmc/articles/PMC3342937/ /pubmed/22570629 http://dx.doi.org/10.1371/journal.pgen.1002658 Text en Wollmann et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Wollmann, Heike
Holec, Sarah
Alden, Keith
Clarke, Neil D.
Jacques, Pierre-Étienne
Berger, Frédéric
Dynamic Deposition of Histone Variant H3.3 Accompanies Developmental Remodeling of the Arabidopsis Transcriptome
title Dynamic Deposition of Histone Variant H3.3 Accompanies Developmental Remodeling of the Arabidopsis Transcriptome
title_full Dynamic Deposition of Histone Variant H3.3 Accompanies Developmental Remodeling of the Arabidopsis Transcriptome
title_fullStr Dynamic Deposition of Histone Variant H3.3 Accompanies Developmental Remodeling of the Arabidopsis Transcriptome
title_full_unstemmed Dynamic Deposition of Histone Variant H3.3 Accompanies Developmental Remodeling of the Arabidopsis Transcriptome
title_short Dynamic Deposition of Histone Variant H3.3 Accompanies Developmental Remodeling of the Arabidopsis Transcriptome
title_sort dynamic deposition of histone variant h3.3 accompanies developmental remodeling of the arabidopsis transcriptome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342937/
https://www.ncbi.nlm.nih.gov/pubmed/22570629
http://dx.doi.org/10.1371/journal.pgen.1002658
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