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Rpd3L HDAC links H3K4me3 to transcriptional repression memory
Transcriptional memory is critical for the faster reactivation of necessary genes upon environmental changes and requires that the genes were previously in an active state. However, whether transcriptional repression also displays ‘memory’ of the prior transcriptionally inactive state remains unknow...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6144869/ https://www.ncbi.nlm.nih.gov/pubmed/29982589 http://dx.doi.org/10.1093/nar/gky573 |
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author | Lee, Bo Bae Choi, Ahyoung Kim, Ji Hyun Jun, Yukyung Woo, Hyeonju Ha, So Dam Yoon, Chae Young Hwang, Jin-Taek Steinmetz, Lars Buratowski, Stephen Lee, Sanghyuk Kim, Hye Young Kim, TaeSoo |
author_facet | Lee, Bo Bae Choi, Ahyoung Kim, Ji Hyun Jun, Yukyung Woo, Hyeonju Ha, So Dam Yoon, Chae Young Hwang, Jin-Taek Steinmetz, Lars Buratowski, Stephen Lee, Sanghyuk Kim, Hye Young Kim, TaeSoo |
author_sort | Lee, Bo Bae |
collection | PubMed |
description | Transcriptional memory is critical for the faster reactivation of necessary genes upon environmental changes and requires that the genes were previously in an active state. However, whether transcriptional repression also displays ‘memory’ of the prior transcriptionally inactive state remains unknown. In this study, we show that transcriptional repression of ∼540 genes in yeast occurs much more rapidly if the genes have been previously repressed during carbon source shifts. This novel transcriptional response has been termed transcriptional repression memory (TREM). Interestingly, Rpd3L histone deacetylase (HDAC), targeted to active promoters induces TREM. Mutants for Rpd3L exhibit increased acetylation at active promoters and delay TREM significantly. Surprisingly, the interaction between H3K4me3 and Rpd3L via the Pho23 PHD finger is critical to promote histone deacetylation and TREM by Rpd3L. Therefore, we propose that an active mark, H3K4me3 enriched at active promoters, instructs Rpd3L HDAC to induce histone deacetylation and TREM. |
format | Online Article Text |
id | pubmed-6144869 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61448692018-09-25 Rpd3L HDAC links H3K4me3 to transcriptional repression memory Lee, Bo Bae Choi, Ahyoung Kim, Ji Hyun Jun, Yukyung Woo, Hyeonju Ha, So Dam Yoon, Chae Young Hwang, Jin-Taek Steinmetz, Lars Buratowski, Stephen Lee, Sanghyuk Kim, Hye Young Kim, TaeSoo Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Transcriptional memory is critical for the faster reactivation of necessary genes upon environmental changes and requires that the genes were previously in an active state. However, whether transcriptional repression also displays ‘memory’ of the prior transcriptionally inactive state remains unknown. In this study, we show that transcriptional repression of ∼540 genes in yeast occurs much more rapidly if the genes have been previously repressed during carbon source shifts. This novel transcriptional response has been termed transcriptional repression memory (TREM). Interestingly, Rpd3L histone deacetylase (HDAC), targeted to active promoters induces TREM. Mutants for Rpd3L exhibit increased acetylation at active promoters and delay TREM significantly. Surprisingly, the interaction between H3K4me3 and Rpd3L via the Pho23 PHD finger is critical to promote histone deacetylation and TREM by Rpd3L. Therefore, we propose that an active mark, H3K4me3 enriched at active promoters, instructs Rpd3L HDAC to induce histone deacetylation and TREM. Oxford University Press 2018-09-19 2018-06-30 /pmc/articles/PMC6144869/ /pubmed/29982589 http://dx.doi.org/10.1093/nar/gky573 Text en © The Author(s) 2018. 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 Lee, Bo Bae Choi, Ahyoung Kim, Ji Hyun Jun, Yukyung Woo, Hyeonju Ha, So Dam Yoon, Chae Young Hwang, Jin-Taek Steinmetz, Lars Buratowski, Stephen Lee, Sanghyuk Kim, Hye Young Kim, TaeSoo Rpd3L HDAC links H3K4me3 to transcriptional repression memory |
title | Rpd3L HDAC links H3K4me3 to transcriptional repression memory |
title_full | Rpd3L HDAC links H3K4me3 to transcriptional repression memory |
title_fullStr | Rpd3L HDAC links H3K4me3 to transcriptional repression memory |
title_full_unstemmed | Rpd3L HDAC links H3K4me3 to transcriptional repression memory |
title_short | Rpd3L HDAC links H3K4me3 to transcriptional repression memory |
title_sort | rpd3l hdac links h3k4me3 to transcriptional repression memory |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6144869/ https://www.ncbi.nlm.nih.gov/pubmed/29982589 http://dx.doi.org/10.1093/nar/gky573 |
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