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The histone variant H2A.Z in yeast is almost exclusively incorporated into the +1 nucleosome in the direction of transcription
Transcription start sites (TSS) in eukaryotes are characterized by a nucleosome-depleted region (NDR), which appears to be flanked upstream and downstream by strongly positioned nucleosomes incorporating the histone variant H2A.Z. H2A.Z associates with both active and repressed TSS and is important...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145542/ https://www.ncbi.nlm.nih.gov/pubmed/31722407 http://dx.doi.org/10.1093/nar/gkz1075 |
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author | Bagchi, Dia N Battenhouse, Anna M Park, Daechan Iyer, Vishwanath R |
author_facet | Bagchi, Dia N Battenhouse, Anna M Park, Daechan Iyer, Vishwanath R |
author_sort | Bagchi, Dia N |
collection | PubMed |
description | Transcription start sites (TSS) in eukaryotes are characterized by a nucleosome-depleted region (NDR), which appears to be flanked upstream and downstream by strongly positioned nucleosomes incorporating the histone variant H2A.Z. H2A.Z associates with both active and repressed TSS and is important for priming genes for rapid transcriptional activation. However, the determinants of H2A.Z occupancy at specific nucleosomes and its relationship to transcription initiation remain unclear. To further elucidate the specificity of H2A.Z, we determined its genomic localization at single nucleosome resolution, as well as the localization of its chromatin remodelers Swr1 and Ino80. By analyzing H2A.Z occupancy in conjunction with RNA expression data that captures promoter-derived antisense initiation, we find that H2A.Z’s bimodal incorporation on either side of the NDR is not a general feature of TSS, but is specifically a marker for bidirectional transcription, such that the upstream flanking −1 H2A.Z-containing nucleosome is more appropriately considered as a +1 H2A.Z nucleosome for antisense transcription. The localization of H2A.Z almost exclusively at the +1 nucleosome suggests that a transcription-initiation dependent process could contribute to its specific incorporation. |
format | Online Article Text |
id | pubmed-7145542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-71455422020-04-13 The histone variant H2A.Z in yeast is almost exclusively incorporated into the +1 nucleosome in the direction of transcription Bagchi, Dia N Battenhouse, Anna M Park, Daechan Iyer, Vishwanath R Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Transcription start sites (TSS) in eukaryotes are characterized by a nucleosome-depleted region (NDR), which appears to be flanked upstream and downstream by strongly positioned nucleosomes incorporating the histone variant H2A.Z. H2A.Z associates with both active and repressed TSS and is important for priming genes for rapid transcriptional activation. However, the determinants of H2A.Z occupancy at specific nucleosomes and its relationship to transcription initiation remain unclear. To further elucidate the specificity of H2A.Z, we determined its genomic localization at single nucleosome resolution, as well as the localization of its chromatin remodelers Swr1 and Ino80. By analyzing H2A.Z occupancy in conjunction with RNA expression data that captures promoter-derived antisense initiation, we find that H2A.Z’s bimodal incorporation on either side of the NDR is not a general feature of TSS, but is specifically a marker for bidirectional transcription, such that the upstream flanking −1 H2A.Z-containing nucleosome is more appropriately considered as a +1 H2A.Z nucleosome for antisense transcription. The localization of H2A.Z almost exclusively at the +1 nucleosome suggests that a transcription-initiation dependent process could contribute to its specific incorporation. Oxford University Press 2020-01-10 2019-11-13 /pmc/articles/PMC7145542/ /pubmed/31722407 http://dx.doi.org/10.1093/nar/gkz1075 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Gene regulation, Chromatin and Epigenetics Bagchi, Dia N Battenhouse, Anna M Park, Daechan Iyer, Vishwanath R The histone variant H2A.Z in yeast is almost exclusively incorporated into the +1 nucleosome in the direction of transcription |
title | The histone variant H2A.Z in yeast is almost exclusively incorporated into the +1 nucleosome in the direction of transcription |
title_full | The histone variant H2A.Z in yeast is almost exclusively incorporated into the +1 nucleosome in the direction of transcription |
title_fullStr | The histone variant H2A.Z in yeast is almost exclusively incorporated into the +1 nucleosome in the direction of transcription |
title_full_unstemmed | The histone variant H2A.Z in yeast is almost exclusively incorporated into the +1 nucleosome in the direction of transcription |
title_short | The histone variant H2A.Z in yeast is almost exclusively incorporated into the +1 nucleosome in the direction of transcription |
title_sort | histone variant h2a.z in yeast is almost exclusively incorporated into the +1 nucleosome in the direction of transcription |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145542/ https://www.ncbi.nlm.nih.gov/pubmed/31722407 http://dx.doi.org/10.1093/nar/gkz1075 |
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