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Functional interaction between the RNA exosome and the sirtuin deacetylase Hst3 maintains transcriptional homeostasis

Eukaryotic cells maintain an optimal level of mRNAs through unknown mechanisms that balance RNA synthesis and degradation. We found that inactivation of the RNA exosome leads to global reduction of nascent mRNA transcripts, and that this defect is accentuated by loss of deposition of histone variant...

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Detalles Bibliográficos
Autores principales: Bryll, Alysia R., Peterson, Craig L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8763048/
https://www.ncbi.nlm.nih.gov/pubmed/34916303
http://dx.doi.org/10.1101/gad.348923.121
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author Bryll, Alysia R.
Peterson, Craig L.
author_facet Bryll, Alysia R.
Peterson, Craig L.
author_sort Bryll, Alysia R.
collection PubMed
description Eukaryotic cells maintain an optimal level of mRNAs through unknown mechanisms that balance RNA synthesis and degradation. We found that inactivation of the RNA exosome leads to global reduction of nascent mRNA transcripts, and that this defect is accentuated by loss of deposition of histone variant H2A.Z. We identify the mRNA for the sirtuin deacetylase Hst3 as a key target for the RNA exosome that mediates communication between RNA degradation and transcription machineries. These findings reveal how the RNA exosome and H2A.Z function together to control a deacetylase, ensuring proper levels of transcription in response to changes in RNA degradation.
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spelling pubmed-87630482022-07-01 Functional interaction between the RNA exosome and the sirtuin deacetylase Hst3 maintains transcriptional homeostasis Bryll, Alysia R. Peterson, Craig L. Genes Dev Research Communication Eukaryotic cells maintain an optimal level of mRNAs through unknown mechanisms that balance RNA synthesis and degradation. We found that inactivation of the RNA exosome leads to global reduction of nascent mRNA transcripts, and that this defect is accentuated by loss of deposition of histone variant H2A.Z. We identify the mRNA for the sirtuin deacetylase Hst3 as a key target for the RNA exosome that mediates communication between RNA degradation and transcription machineries. These findings reveal how the RNA exosome and H2A.Z function together to control a deacetylase, ensuring proper levels of transcription in response to changes in RNA degradation. Cold Spring Harbor Laboratory Press 2022-01-01 /pmc/articles/PMC8763048/ /pubmed/34916303 http://dx.doi.org/10.1101/gad.348923.121 Text en © 2022 Bryll and Peterson; Published by Cold Spring Harbor Laboratory Press https://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/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Research Communication
Bryll, Alysia R.
Peterson, Craig L.
Functional interaction between the RNA exosome and the sirtuin deacetylase Hst3 maintains transcriptional homeostasis
title Functional interaction between the RNA exosome and the sirtuin deacetylase Hst3 maintains transcriptional homeostasis
title_full Functional interaction between the RNA exosome and the sirtuin deacetylase Hst3 maintains transcriptional homeostasis
title_fullStr Functional interaction between the RNA exosome and the sirtuin deacetylase Hst3 maintains transcriptional homeostasis
title_full_unstemmed Functional interaction between the RNA exosome and the sirtuin deacetylase Hst3 maintains transcriptional homeostasis
title_short Functional interaction between the RNA exosome and the sirtuin deacetylase Hst3 maintains transcriptional homeostasis
title_sort functional interaction between the rna exosome and the sirtuin deacetylase hst3 maintains transcriptional homeostasis
topic Research Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8763048/
https://www.ncbi.nlm.nih.gov/pubmed/34916303
http://dx.doi.org/10.1101/gad.348923.121
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