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Despite its sequence identity with canonical H4, Drosophila H4r product is enriched at specific chromatin regions

Histone variants are different from their canonical counterparts in structure and are encoded by solitary genes with unique regulation to fulfill tissue or differentiation specific functions. A single H4 variant gene (His4r or H4r) that is located outside of the histone cluster and gives rise to a p...

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Autores principales: Ábrahám, Andrea, Villányi, Zoltán, Zsindely, Nóra, Nagy, Gábor, Szabó, Áron, Bodai, László, Henn, László, Boros, Imre M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8943024/
https://www.ncbi.nlm.nih.gov/pubmed/35322122
http://dx.doi.org/10.1038/s41598-022-09026-x
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author Ábrahám, Andrea
Villányi, Zoltán
Zsindely, Nóra
Nagy, Gábor
Szabó, Áron
Bodai, László
Henn, László
Boros, Imre M.
author_facet Ábrahám, Andrea
Villányi, Zoltán
Zsindely, Nóra
Nagy, Gábor
Szabó, Áron
Bodai, László
Henn, László
Boros, Imre M.
author_sort Ábrahám, Andrea
collection PubMed
description Histone variants are different from their canonical counterparts in structure and are encoded by solitary genes with unique regulation to fulfill tissue or differentiation specific functions. A single H4 variant gene (His4r or H4r) that is located outside of the histone cluster and gives rise to a polyA tailed messenger RNA via replication-independent expression is preserved in Drosophila strains despite that its protein product is identical with canonical H4. In order to reveal information on the possible role of this alternative H4 we epitope tagged endogenous H4r and studied its spatial and temporal expression, and revealed its genome-wide localization to chromatin at the nucleosomal level. RNA and immunohistochemistry analysis of H4r expressed under its cognate regulation indicate expression of the gene throughout zygotic and larval development and presence of the protein product is evident already in the pronuclei of fertilized eggs. In the developing nervous system a slight disequibrium in H4r distribution is observable, cholinergic neurons are the most abundant among H4r-expressing cells. ChIP-seq experiments revealed H4r association with regulatory regions of genes involved in cellular stress response. The data presented here indicate that H4r has a variant histone function.
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spelling pubmed-89430242022-03-28 Despite its sequence identity with canonical H4, Drosophila H4r product is enriched at specific chromatin regions Ábrahám, Andrea Villányi, Zoltán Zsindely, Nóra Nagy, Gábor Szabó, Áron Bodai, László Henn, László Boros, Imre M. Sci Rep Article Histone variants are different from their canonical counterparts in structure and are encoded by solitary genes with unique regulation to fulfill tissue or differentiation specific functions. A single H4 variant gene (His4r or H4r) that is located outside of the histone cluster and gives rise to a polyA tailed messenger RNA via replication-independent expression is preserved in Drosophila strains despite that its protein product is identical with canonical H4. In order to reveal information on the possible role of this alternative H4 we epitope tagged endogenous H4r and studied its spatial and temporal expression, and revealed its genome-wide localization to chromatin at the nucleosomal level. RNA and immunohistochemistry analysis of H4r expressed under its cognate regulation indicate expression of the gene throughout zygotic and larval development and presence of the protein product is evident already in the pronuclei of fertilized eggs. In the developing nervous system a slight disequibrium in H4r distribution is observable, cholinergic neurons are the most abundant among H4r-expressing cells. ChIP-seq experiments revealed H4r association with regulatory regions of genes involved in cellular stress response. The data presented here indicate that H4r has a variant histone function. Nature Publishing Group UK 2022-03-23 /pmc/articles/PMC8943024/ /pubmed/35322122 http://dx.doi.org/10.1038/s41598-022-09026-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ábrahám, Andrea
Villányi, Zoltán
Zsindely, Nóra
Nagy, Gábor
Szabó, Áron
Bodai, László
Henn, László
Boros, Imre M.
Despite its sequence identity with canonical H4, Drosophila H4r product is enriched at specific chromatin regions
title Despite its sequence identity with canonical H4, Drosophila H4r product is enriched at specific chromatin regions
title_full Despite its sequence identity with canonical H4, Drosophila H4r product is enriched at specific chromatin regions
title_fullStr Despite its sequence identity with canonical H4, Drosophila H4r product is enriched at specific chromatin regions
title_full_unstemmed Despite its sequence identity with canonical H4, Drosophila H4r product is enriched at specific chromatin regions
title_short Despite its sequence identity with canonical H4, Drosophila H4r product is enriched at specific chromatin regions
title_sort despite its sequence identity with canonical h4, drosophila h4r product is enriched at specific chromatin regions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8943024/
https://www.ncbi.nlm.nih.gov/pubmed/35322122
http://dx.doi.org/10.1038/s41598-022-09026-x
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