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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
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.
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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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