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Unveiling RCOR1 as a rheostat at transcriptionally permissive chromatin
RCOR1 is a known transcription repressor that recruits and positions LSD1 and HDAC1/2 on chromatin to erase histone methylation and acetylation. However, there is currently an incomplete understanding of RCOR1’s range of localization and function. Here, we probe RCOR1’s distribution on a genome-wide...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8943175/ https://www.ncbi.nlm.nih.gov/pubmed/35322029 http://dx.doi.org/10.1038/s41467-022-29261-0 |
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author | Rivera, Carlos Lee, Hun-Goo Lappala, Anna Wang, Danni Noches, Verónica Olivares-Costa, Montserrat Sjöberg-Herrera, Marcela Lee, Jeannie T. Andrés, María Estela |
author_facet | Rivera, Carlos Lee, Hun-Goo Lappala, Anna Wang, Danni Noches, Verónica Olivares-Costa, Montserrat Sjöberg-Herrera, Marcela Lee, Jeannie T. Andrés, María Estela |
author_sort | Rivera, Carlos |
collection | PubMed |
description | RCOR1 is a known transcription repressor that recruits and positions LSD1 and HDAC1/2 on chromatin to erase histone methylation and acetylation. However, there is currently an incomplete understanding of RCOR1’s range of localization and function. Here, we probe RCOR1’s distribution on a genome-wide scale and unexpectedly find that RCOR1 is predominantly associated with transcriptionally active genes. Biochemical analysis reveals that RCOR1 associates with RNA Polymerase II (POL-II) during transcription and deacetylates its carboxy-terminal domain (CTD) at lysine 7. We provide evidence that this non-canonical RCOR1 activity is linked to dampening of POL-II productive elongation at actively transcribing genes. Thus, RCOR1 represses transcription in two ways—first, via a canonical mechanism by erasing transcriptionally permissive histone modifications through associating with HDACs and, second, via a non-canonical mechanism that deacetylates RNA POL-II’s CTD to inhibit productive elongation. We conclude that RCOR1 is a transcription rheostat. |
format | Online Article Text |
id | pubmed-8943175 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89431752022-04-08 Unveiling RCOR1 as a rheostat at transcriptionally permissive chromatin Rivera, Carlos Lee, Hun-Goo Lappala, Anna Wang, Danni Noches, Verónica Olivares-Costa, Montserrat Sjöberg-Herrera, Marcela Lee, Jeannie T. Andrés, María Estela Nat Commun Article RCOR1 is a known transcription repressor that recruits and positions LSD1 and HDAC1/2 on chromatin to erase histone methylation and acetylation. However, there is currently an incomplete understanding of RCOR1’s range of localization and function. Here, we probe RCOR1’s distribution on a genome-wide scale and unexpectedly find that RCOR1 is predominantly associated with transcriptionally active genes. Biochemical analysis reveals that RCOR1 associates with RNA Polymerase II (POL-II) during transcription and deacetylates its carboxy-terminal domain (CTD) at lysine 7. We provide evidence that this non-canonical RCOR1 activity is linked to dampening of POL-II productive elongation at actively transcribing genes. Thus, RCOR1 represses transcription in two ways—first, via a canonical mechanism by erasing transcriptionally permissive histone modifications through associating with HDACs and, second, via a non-canonical mechanism that deacetylates RNA POL-II’s CTD to inhibit productive elongation. We conclude that RCOR1 is a transcription rheostat. Nature Publishing Group UK 2022-03-23 /pmc/articles/PMC8943175/ /pubmed/35322029 http://dx.doi.org/10.1038/s41467-022-29261-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Rivera, Carlos Lee, Hun-Goo Lappala, Anna Wang, Danni Noches, Verónica Olivares-Costa, Montserrat Sjöberg-Herrera, Marcela Lee, Jeannie T. Andrés, María Estela Unveiling RCOR1 as a rheostat at transcriptionally permissive chromatin |
title | Unveiling RCOR1 as a rheostat at transcriptionally permissive chromatin |
title_full | Unveiling RCOR1 as a rheostat at transcriptionally permissive chromatin |
title_fullStr | Unveiling RCOR1 as a rheostat at transcriptionally permissive chromatin |
title_full_unstemmed | Unveiling RCOR1 as a rheostat at transcriptionally permissive chromatin |
title_short | Unveiling RCOR1 as a rheostat at transcriptionally permissive chromatin |
title_sort | unveiling rcor1 as a rheostat at transcriptionally permissive chromatin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8943175/ https://www.ncbi.nlm.nih.gov/pubmed/35322029 http://dx.doi.org/10.1038/s41467-022-29261-0 |
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