Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Bagchi, Dia N, Battenhouse, Anna M, Park, Daechan, Iyer, Vishwanath R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
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
_version_ 1783520010786832384
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
work_keys_str_mv AT bagchidian thehistonevarianth2azinyeastisalmostexclusivelyincorporatedintothe1nucleosomeinthedirectionoftranscription
AT battenhouseannam thehistonevarianth2azinyeastisalmostexclusivelyincorporatedintothe1nucleosomeinthedirectionoftranscription
AT parkdaechan thehistonevarianth2azinyeastisalmostexclusivelyincorporatedintothe1nucleosomeinthedirectionoftranscription
AT iyervishwanathr thehistonevarianth2azinyeastisalmostexclusivelyincorporatedintothe1nucleosomeinthedirectionoftranscription
AT bagchidian histonevarianth2azinyeastisalmostexclusivelyincorporatedintothe1nucleosomeinthedirectionoftranscription
AT battenhouseannam histonevarianth2azinyeastisalmostexclusivelyincorporatedintothe1nucleosomeinthedirectionoftranscription
AT parkdaechan histonevarianth2azinyeastisalmostexclusivelyincorporatedintothe1nucleosomeinthedirectionoftranscription
AT iyervishwanathr histonevarianth2azinyeastisalmostexclusivelyincorporatedintothe1nucleosomeinthedirectionoftranscription