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Myosin VI regulates the spatial organisation of mammalian transcription initiation
During transcription, RNA Polymerase II (RNAPII) is spatially organised within the nucleus into clusters that correlate with transcription activity. While this is a hallmark of genome regulation in mammalian cells, the mechanisms concerning the assembly, organisation and stability remain unknown. He...
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/PMC8924246/ https://www.ncbi.nlm.nih.gov/pubmed/35292632 http://dx.doi.org/10.1038/s41467-022-28962-w |
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author | Hari-Gupta, Yukti Fili, Natalia dos Santos, Ália Cook, Alexander W. Gough, Rosemarie E. Reed, Hannah C. W. Wang, Lin Aaron, Jesse Venit, Tomas Wait, Eric Grosse-Berkenbusch, Andreas Gebhardt, J. Christof M. Percipalle, Piergiorgio Chew, Teng-Leong Martin-Fernandez, Marisa Toseland, Christopher P. |
author_facet | Hari-Gupta, Yukti Fili, Natalia dos Santos, Ália Cook, Alexander W. Gough, Rosemarie E. Reed, Hannah C. W. Wang, Lin Aaron, Jesse Venit, Tomas Wait, Eric Grosse-Berkenbusch, Andreas Gebhardt, J. Christof M. Percipalle, Piergiorgio Chew, Teng-Leong Martin-Fernandez, Marisa Toseland, Christopher P. |
author_sort | Hari-Gupta, Yukti |
collection | PubMed |
description | During transcription, RNA Polymerase II (RNAPII) is spatially organised within the nucleus into clusters that correlate with transcription activity. While this is a hallmark of genome regulation in mammalian cells, the mechanisms concerning the assembly, organisation and stability remain unknown. Here, we have used combination of single molecule imaging and genomic approaches to explore the role of nuclear myosin VI (MVI) in the nanoscale organisation of RNAPII. We reveal that MVI in the nucleus acts as the molecular anchor that holds RNAPII in high density clusters. Perturbation of MVI leads to the disruption of RNAPII localisation, chromatin organisation and subsequently a decrease in gene expression. Overall, we uncover the fundamental role of MVI in the spatial regulation of gene expression. |
format | Online Article Text |
id | pubmed-8924246 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89242462022-04-01 Myosin VI regulates the spatial organisation of mammalian transcription initiation Hari-Gupta, Yukti Fili, Natalia dos Santos, Ália Cook, Alexander W. Gough, Rosemarie E. Reed, Hannah C. W. Wang, Lin Aaron, Jesse Venit, Tomas Wait, Eric Grosse-Berkenbusch, Andreas Gebhardt, J. Christof M. Percipalle, Piergiorgio Chew, Teng-Leong Martin-Fernandez, Marisa Toseland, Christopher P. Nat Commun Article During transcription, RNA Polymerase II (RNAPII) is spatially organised within the nucleus into clusters that correlate with transcription activity. While this is a hallmark of genome regulation in mammalian cells, the mechanisms concerning the assembly, organisation and stability remain unknown. Here, we have used combination of single molecule imaging and genomic approaches to explore the role of nuclear myosin VI (MVI) in the nanoscale organisation of RNAPII. We reveal that MVI in the nucleus acts as the molecular anchor that holds RNAPII in high density clusters. Perturbation of MVI leads to the disruption of RNAPII localisation, chromatin organisation and subsequently a decrease in gene expression. Overall, we uncover the fundamental role of MVI in the spatial regulation of gene expression. Nature Publishing Group UK 2022-03-15 /pmc/articles/PMC8924246/ /pubmed/35292632 http://dx.doi.org/10.1038/s41467-022-28962-w 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 Hari-Gupta, Yukti Fili, Natalia dos Santos, Ália Cook, Alexander W. Gough, Rosemarie E. Reed, Hannah C. W. Wang, Lin Aaron, Jesse Venit, Tomas Wait, Eric Grosse-Berkenbusch, Andreas Gebhardt, J. Christof M. Percipalle, Piergiorgio Chew, Teng-Leong Martin-Fernandez, Marisa Toseland, Christopher P. Myosin VI regulates the spatial organisation of mammalian transcription initiation |
title | Myosin VI regulates the spatial organisation of mammalian transcription initiation |
title_full | Myosin VI regulates the spatial organisation of mammalian transcription initiation |
title_fullStr | Myosin VI regulates the spatial organisation of mammalian transcription initiation |
title_full_unstemmed | Myosin VI regulates the spatial organisation of mammalian transcription initiation |
title_short | Myosin VI regulates the spatial organisation of mammalian transcription initiation |
title_sort | myosin vi regulates the spatial organisation of mammalian transcription initiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924246/ https://www.ncbi.nlm.nih.gov/pubmed/35292632 http://dx.doi.org/10.1038/s41467-022-28962-w |
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