Cargando…

Nucleosome alterations caused by mutations at modifiable histone residues in Saccharomyces cerevisiae

Nucleosome organization exhibits dynamic properties depending on the cell state and environment. Histone proteins, fundamental components of nucleosomes, are subject to chemical modifications on particular residues. We examined the effect of substituting modifiable residues of four core histones wit...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Hongde, Wang, Pingyan, Liu, Lingjie, Min, Zhu, Luo, Kun, Wan, Yakun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620441/
https://www.ncbi.nlm.nih.gov/pubmed/26498326
http://dx.doi.org/10.1038/srep15583
_version_ 1782397297947049984
author Liu, Hongde
Wang, Pingyan
Liu, Lingjie
Min, Zhu
Luo, Kun
Wan, Yakun
author_facet Liu, Hongde
Wang, Pingyan
Liu, Lingjie
Min, Zhu
Luo, Kun
Wan, Yakun
author_sort Liu, Hongde
collection PubMed
description Nucleosome organization exhibits dynamic properties depending on the cell state and environment. Histone proteins, fundamental components of nucleosomes, are subject to chemical modifications on particular residues. We examined the effect of substituting modifiable residues of four core histones with the non-modifiable residue alanine on nucleosome dynamics. We mapped the genome-wide nucleosomes in 22 histone mutants of Saccharomyces cerevisiae and compared the nucleosome alterations relative to the wild-type strain. Our results indicated that different types of histone mutation resulted in different phenotypes and a distinct reorganization of nucleosomes. Nucleosome occupancy was altered at telomeres, but not at centromeres. The first nucleosomes upstream (−1) and downstream (+1) of the transcription start site (TSS) were more dynamic than other nucleosomes. Mutations in histones affected the nucleosome array downstream of the TSS. Highly expressed genes, such as ribosome genes and genes involved in glycolysis, showed increased nucleosome occupancy in many types of histone mutant. In particular, the H3K56A mutant exhibited a high percentage of dynamic genomic regions, decreased nucleosome occupancy at telomeres, increased occupancy at the +1 and −1 nucleosomes, and a slow growth phenotype under stress conditions. Our findings provide insight into the influence of histone mutations on nucleosome dynamics.
format Online
Article
Text
id pubmed-4620441
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-46204412015-10-29 Nucleosome alterations caused by mutations at modifiable histone residues in Saccharomyces cerevisiae Liu, Hongde Wang, Pingyan Liu, Lingjie Min, Zhu Luo, Kun Wan, Yakun Sci Rep Article Nucleosome organization exhibits dynamic properties depending on the cell state and environment. Histone proteins, fundamental components of nucleosomes, are subject to chemical modifications on particular residues. We examined the effect of substituting modifiable residues of four core histones with the non-modifiable residue alanine on nucleosome dynamics. We mapped the genome-wide nucleosomes in 22 histone mutants of Saccharomyces cerevisiae and compared the nucleosome alterations relative to the wild-type strain. Our results indicated that different types of histone mutation resulted in different phenotypes and a distinct reorganization of nucleosomes. Nucleosome occupancy was altered at telomeres, but not at centromeres. The first nucleosomes upstream (−1) and downstream (+1) of the transcription start site (TSS) were more dynamic than other nucleosomes. Mutations in histones affected the nucleosome array downstream of the TSS. Highly expressed genes, such as ribosome genes and genes involved in glycolysis, showed increased nucleosome occupancy in many types of histone mutant. In particular, the H3K56A mutant exhibited a high percentage of dynamic genomic regions, decreased nucleosome occupancy at telomeres, increased occupancy at the +1 and −1 nucleosomes, and a slow growth phenotype under stress conditions. Our findings provide insight into the influence of histone mutations on nucleosome dynamics. Nature Publishing Group 2015-10-26 /pmc/articles/PMC4620441/ /pubmed/26498326 http://dx.doi.org/10.1038/srep15583 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Liu, Hongde
Wang, Pingyan
Liu, Lingjie
Min, Zhu
Luo, Kun
Wan, Yakun
Nucleosome alterations caused by mutations at modifiable histone residues in Saccharomyces cerevisiae
title Nucleosome alterations caused by mutations at modifiable histone residues in Saccharomyces cerevisiae
title_full Nucleosome alterations caused by mutations at modifiable histone residues in Saccharomyces cerevisiae
title_fullStr Nucleosome alterations caused by mutations at modifiable histone residues in Saccharomyces cerevisiae
title_full_unstemmed Nucleosome alterations caused by mutations at modifiable histone residues in Saccharomyces cerevisiae
title_short Nucleosome alterations caused by mutations at modifiable histone residues in Saccharomyces cerevisiae
title_sort nucleosome alterations caused by mutations at modifiable histone residues in saccharomyces cerevisiae
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620441/
https://www.ncbi.nlm.nih.gov/pubmed/26498326
http://dx.doi.org/10.1038/srep15583
work_keys_str_mv AT liuhongde nucleosomealterationscausedbymutationsatmodifiablehistoneresiduesinsaccharomycescerevisiae
AT wangpingyan nucleosomealterationscausedbymutationsatmodifiablehistoneresiduesinsaccharomycescerevisiae
AT liulingjie nucleosomealterationscausedbymutationsatmodifiablehistoneresiduesinsaccharomycescerevisiae
AT minzhu nucleosomealterationscausedbymutationsatmodifiablehistoneresiduesinsaccharomycescerevisiae
AT luokun nucleosomealterationscausedbymutationsatmodifiablehistoneresiduesinsaccharomycescerevisiae
AT wanyakun nucleosomealterationscausedbymutationsatmodifiablehistoneresiduesinsaccharomycescerevisiae