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Anti-silencing factor Epe1 associates with SAGA to regulate transcription within heterochromatin
Heterochromatin is a highly condensed form of chromatin that silences gene transcription. Although high levels of transcriptional activities disrupt heterochromatin, transcription of repetitive DNA elements and subsequent processing of the transcripts by the RNAi machinery are required for heterochr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6317313/ https://www.ncbi.nlm.nih.gov/pubmed/30573453 http://dx.doi.org/10.1101/gad.318030.118 |
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author | Bao, Kehan Shan, Chun-Min Moresco, James Yates, John Jia, Songtao |
author_facet | Bao, Kehan Shan, Chun-Min Moresco, James Yates, John Jia, Songtao |
author_sort | Bao, Kehan |
collection | PubMed |
description | Heterochromatin is a highly condensed form of chromatin that silences gene transcription. Although high levels of transcriptional activities disrupt heterochromatin, transcription of repetitive DNA elements and subsequent processing of the transcripts by the RNAi machinery are required for heterochromatin assembly. In fission yeast, a JmjC domain protein, Epe1, promotes transcription of DNA repeats to facilitate heterochromatin formation, but overexpression of Epe1 leads to heterochromatin defects. However, the molecular function of Epe1 is not well understood. By screening the fission yeast deletion library, we found that heterochromatin defects associated with Epe1 overexpression are alleviated by mutations of the SAGA histone acetyltransferase complex. Overexpressed Epe1 associates with SAGA and recruits SAGA to heterochromatin regions, which leads to increased histone acetylation, transcription of repeats, and the disruption of heterochromatin. At its normal expression levels, Epe1 also associates with SAGA, albeit weakly. Such interaction regulates histone acetylation levels at heterochromatin and promotes transcription of repeats for heterochromatin assembly. Our results also suggest that increases of certain chromatin protein levels, which frequently occur in cancer cells, might strengthen relatively weak interactions to affect the epigenetic landscape. |
format | Online Article Text |
id | pubmed-6317313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63173132019-07-01 Anti-silencing factor Epe1 associates with SAGA to regulate transcription within heterochromatin Bao, Kehan Shan, Chun-Min Moresco, James Yates, John Jia, Songtao Genes Dev Research Paper Heterochromatin is a highly condensed form of chromatin that silences gene transcription. Although high levels of transcriptional activities disrupt heterochromatin, transcription of repetitive DNA elements and subsequent processing of the transcripts by the RNAi machinery are required for heterochromatin assembly. In fission yeast, a JmjC domain protein, Epe1, promotes transcription of DNA repeats to facilitate heterochromatin formation, but overexpression of Epe1 leads to heterochromatin defects. However, the molecular function of Epe1 is not well understood. By screening the fission yeast deletion library, we found that heterochromatin defects associated with Epe1 overexpression are alleviated by mutations of the SAGA histone acetyltransferase complex. Overexpressed Epe1 associates with SAGA and recruits SAGA to heterochromatin regions, which leads to increased histone acetylation, transcription of repeats, and the disruption of heterochromatin. At its normal expression levels, Epe1 also associates with SAGA, albeit weakly. Such interaction regulates histone acetylation levels at heterochromatin and promotes transcription of repeats for heterochromatin assembly. Our results also suggest that increases of certain chromatin protein levels, which frequently occur in cancer cells, might strengthen relatively weak interactions to affect the epigenetic landscape. Cold Spring Harbor Laboratory Press 2019-01-01 /pmc/articles/PMC6317313/ /pubmed/30573453 http://dx.doi.org/10.1101/gad.318030.118 Text en © 2019 Bao, et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Research Paper Bao, Kehan Shan, Chun-Min Moresco, James Yates, John Jia, Songtao Anti-silencing factor Epe1 associates with SAGA to regulate transcription within heterochromatin |
title | Anti-silencing factor Epe1 associates with SAGA to regulate transcription within heterochromatin |
title_full | Anti-silencing factor Epe1 associates with SAGA to regulate transcription within heterochromatin |
title_fullStr | Anti-silencing factor Epe1 associates with SAGA to regulate transcription within heterochromatin |
title_full_unstemmed | Anti-silencing factor Epe1 associates with SAGA to regulate transcription within heterochromatin |
title_short | Anti-silencing factor Epe1 associates with SAGA to regulate transcription within heterochromatin |
title_sort | anti-silencing factor epe1 associates with saga to regulate transcription within heterochromatin |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6317313/ https://www.ncbi.nlm.nih.gov/pubmed/30573453 http://dx.doi.org/10.1101/gad.318030.118 |
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