Cargando…

The Hda1 histone deacetylase limits divergent non‐coding transcription and restricts transcription initiation frequency

Nucleosome‐depleted regions (NDRs) at gene promoters support initiation of RNA polymerase II transcription. Interestingly, transcription often initiates in both directions, resulting in an mRNA and a divergent non‐coding (DNC) transcript of unclear purpose. Here, we characterized the genetic archite...

Descripción completa

Detalles Bibliográficos
Autores principales: Gowthaman, Uthra, Ivanov, Maxim, Schwarz, Isabel, Patel, Heta P, Müller, Niels A, García‐Pichardo, Desiré, Lenstra, Tineke L, Marquardt, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8634119/
https://www.ncbi.nlm.nih.gov/pubmed/34661296
http://dx.doi.org/10.15252/embj.2021108903
_version_ 1784608073335177216
author Gowthaman, Uthra
Ivanov, Maxim
Schwarz, Isabel
Patel, Heta P
Müller, Niels A
García‐Pichardo, Desiré
Lenstra, Tineke L
Marquardt, Sebastian
author_facet Gowthaman, Uthra
Ivanov, Maxim
Schwarz, Isabel
Patel, Heta P
Müller, Niels A
García‐Pichardo, Desiré
Lenstra, Tineke L
Marquardt, Sebastian
author_sort Gowthaman, Uthra
collection PubMed
description Nucleosome‐depleted regions (NDRs) at gene promoters support initiation of RNA polymerase II transcription. Interestingly, transcription often initiates in both directions, resulting in an mRNA and a divergent non‐coding (DNC) transcript of unclear purpose. Here, we characterized the genetic architecture and molecular mechanism of DNC transcription in budding yeast. Using high‐throughput reverse genetic screens based on quantitative single‐cell fluorescence measurements, we identified the Hda1 histone deacetylase complex (Hda1C) as a repressor of DNC transcription. Nascent transcription profiling showed a genome‐wide role of Hda1C in repression of DNC transcription. Live‐cell imaging of transcription revealed that mutations in the Hda3 subunit increased the frequency of DNC transcription. Hda1C contributed to decreased acetylation of histone H3 in DNC transcription regions, supporting DNC transcription repression by histone deacetylation. Our data support the interpretation that DNC transcription results as a consequence of the NDR‐based architecture of eukaryotic promoters, but that it is governed by locus‐specific repression to maintain genome fidelity.
format Online
Article
Text
id pubmed-8634119
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-86341192021-12-20 The Hda1 histone deacetylase limits divergent non‐coding transcription and restricts transcription initiation frequency Gowthaman, Uthra Ivanov, Maxim Schwarz, Isabel Patel, Heta P Müller, Niels A García‐Pichardo, Desiré Lenstra, Tineke L Marquardt, Sebastian EMBO J Articles Nucleosome‐depleted regions (NDRs) at gene promoters support initiation of RNA polymerase II transcription. Interestingly, transcription often initiates in both directions, resulting in an mRNA and a divergent non‐coding (DNC) transcript of unclear purpose. Here, we characterized the genetic architecture and molecular mechanism of DNC transcription in budding yeast. Using high‐throughput reverse genetic screens based on quantitative single‐cell fluorescence measurements, we identified the Hda1 histone deacetylase complex (Hda1C) as a repressor of DNC transcription. Nascent transcription profiling showed a genome‐wide role of Hda1C in repression of DNC transcription. Live‐cell imaging of transcription revealed that mutations in the Hda3 subunit increased the frequency of DNC transcription. Hda1C contributed to decreased acetylation of histone H3 in DNC transcription regions, supporting DNC transcription repression by histone deacetylation. Our data support the interpretation that DNC transcription results as a consequence of the NDR‐based architecture of eukaryotic promoters, but that it is governed by locus‐specific repression to maintain genome fidelity. John Wiley and Sons Inc. 2021-10-18 2021-12-01 /pmc/articles/PMC8634119/ /pubmed/34661296 http://dx.doi.org/10.15252/embj.2021108903 Text en © 2021 The Authors. Published under the terms of the CC BY NC ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Articles
Gowthaman, Uthra
Ivanov, Maxim
Schwarz, Isabel
Patel, Heta P
Müller, Niels A
García‐Pichardo, Desiré
Lenstra, Tineke L
Marquardt, Sebastian
The Hda1 histone deacetylase limits divergent non‐coding transcription and restricts transcription initiation frequency
title The Hda1 histone deacetylase limits divergent non‐coding transcription and restricts transcription initiation frequency
title_full The Hda1 histone deacetylase limits divergent non‐coding transcription and restricts transcription initiation frequency
title_fullStr The Hda1 histone deacetylase limits divergent non‐coding transcription and restricts transcription initiation frequency
title_full_unstemmed The Hda1 histone deacetylase limits divergent non‐coding transcription and restricts transcription initiation frequency
title_short The Hda1 histone deacetylase limits divergent non‐coding transcription and restricts transcription initiation frequency
title_sort hda1 histone deacetylase limits divergent non‐coding transcription and restricts transcription initiation frequency
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8634119/
https://www.ncbi.nlm.nih.gov/pubmed/34661296
http://dx.doi.org/10.15252/embj.2021108903
work_keys_str_mv AT gowthamanuthra thehda1histonedeacetylaselimitsdivergentnoncodingtranscriptionandrestrictstranscriptioninitiationfrequency
AT ivanovmaxim thehda1histonedeacetylaselimitsdivergentnoncodingtranscriptionandrestrictstranscriptioninitiationfrequency
AT schwarzisabel thehda1histonedeacetylaselimitsdivergentnoncodingtranscriptionandrestrictstranscriptioninitiationfrequency
AT patelhetap thehda1histonedeacetylaselimitsdivergentnoncodingtranscriptionandrestrictstranscriptioninitiationfrequency
AT mullernielsa thehda1histonedeacetylaselimitsdivergentnoncodingtranscriptionandrestrictstranscriptioninitiationfrequency
AT garciapichardodesire thehda1histonedeacetylaselimitsdivergentnoncodingtranscriptionandrestrictstranscriptioninitiationfrequency
AT lenstratinekel thehda1histonedeacetylaselimitsdivergentnoncodingtranscriptionandrestrictstranscriptioninitiationfrequency
AT marquardtsebastian thehda1histonedeacetylaselimitsdivergentnoncodingtranscriptionandrestrictstranscriptioninitiationfrequency
AT gowthamanuthra hda1histonedeacetylaselimitsdivergentnoncodingtranscriptionandrestrictstranscriptioninitiationfrequency
AT ivanovmaxim hda1histonedeacetylaselimitsdivergentnoncodingtranscriptionandrestrictstranscriptioninitiationfrequency
AT schwarzisabel hda1histonedeacetylaselimitsdivergentnoncodingtranscriptionandrestrictstranscriptioninitiationfrequency
AT patelhetap hda1histonedeacetylaselimitsdivergentnoncodingtranscriptionandrestrictstranscriptioninitiationfrequency
AT mullernielsa hda1histonedeacetylaselimitsdivergentnoncodingtranscriptionandrestrictstranscriptioninitiationfrequency
AT garciapichardodesire hda1histonedeacetylaselimitsdivergentnoncodingtranscriptionandrestrictstranscriptioninitiationfrequency
AT lenstratinekel hda1histonedeacetylaselimitsdivergentnoncodingtranscriptionandrestrictstranscriptioninitiationfrequency
AT marquardtsebastian hda1histonedeacetylaselimitsdivergentnoncodingtranscriptionandrestrictstranscriptioninitiationfrequency