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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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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 |
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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 |
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