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RNA polymerase II depletion from the inactive X chromosome territory is not mediated by physical compartmentalization

Subnuclear compartmentalization has been proposed to play an important role in gene regulation by segregating active and inactive parts of the genome in distinct physical and biochemical environments. During X chromosome inactivation (XCI), the noncoding Xist RNA coats the X chromosome, triggers gen...

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Autores principales: Collombet, Samuel, Rall, Isabell, Dugast-Darzacq, Claire, Heckert, Alec, Halavatyi, Aliaksandr, Le Saux, Agnes, Dailey, Gina, Darzacq, Xavier, Heard, Edith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10442225/
https://www.ncbi.nlm.nih.gov/pubmed/37291424
http://dx.doi.org/10.1038/s41594-023-01008-5
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author Collombet, Samuel
Rall, Isabell
Dugast-Darzacq, Claire
Heckert, Alec
Halavatyi, Aliaksandr
Le Saux, Agnes
Dailey, Gina
Darzacq, Xavier
Heard, Edith
author_facet Collombet, Samuel
Rall, Isabell
Dugast-Darzacq, Claire
Heckert, Alec
Halavatyi, Aliaksandr
Le Saux, Agnes
Dailey, Gina
Darzacq, Xavier
Heard, Edith
author_sort Collombet, Samuel
collection PubMed
description Subnuclear compartmentalization has been proposed to play an important role in gene regulation by segregating active and inactive parts of the genome in distinct physical and biochemical environments. During X chromosome inactivation (XCI), the noncoding Xist RNA coats the X chromosome, triggers gene silencing and forms a dense body of heterochromatin from which the transcription machinery appears to be excluded. Phase separation has been proposed to be involved in XCI, and might explain the exclusion of the transcription machinery by preventing its diffusion into the Xist-coated territory. Here, using quantitative fluorescence microscopy and single-particle tracking, we show that RNA polymerase II (RNAPII) freely accesses the Xist territory during the initiation of XCI. Instead, the apparent depletion of RNAPII is due to the loss of its chromatin stably bound fraction. These findings indicate that initial exclusion of RNAPII from the inactive X reflects the absence of actively transcribing RNAPII, rather than a consequence of putative physical compartmentalization of the inactive X heterochromatin domain.
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spelling pubmed-104422252023-08-23 RNA polymerase II depletion from the inactive X chromosome territory is not mediated by physical compartmentalization Collombet, Samuel Rall, Isabell Dugast-Darzacq, Claire Heckert, Alec Halavatyi, Aliaksandr Le Saux, Agnes Dailey, Gina Darzacq, Xavier Heard, Edith Nat Struct Mol Biol Article Subnuclear compartmentalization has been proposed to play an important role in gene regulation by segregating active and inactive parts of the genome in distinct physical and biochemical environments. During X chromosome inactivation (XCI), the noncoding Xist RNA coats the X chromosome, triggers gene silencing and forms a dense body of heterochromatin from which the transcription machinery appears to be excluded. Phase separation has been proposed to be involved in XCI, and might explain the exclusion of the transcription machinery by preventing its diffusion into the Xist-coated territory. Here, using quantitative fluorescence microscopy and single-particle tracking, we show that RNA polymerase II (RNAPII) freely accesses the Xist territory during the initiation of XCI. Instead, the apparent depletion of RNAPII is due to the loss of its chromatin stably bound fraction. These findings indicate that initial exclusion of RNAPII from the inactive X reflects the absence of actively transcribing RNAPII, rather than a consequence of putative physical compartmentalization of the inactive X heterochromatin domain. Nature Publishing Group US 2023-06-08 2023 /pmc/articles/PMC10442225/ /pubmed/37291424 http://dx.doi.org/10.1038/s41594-023-01008-5 Text en © The Author(s) 2023 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
Collombet, Samuel
Rall, Isabell
Dugast-Darzacq, Claire
Heckert, Alec
Halavatyi, Aliaksandr
Le Saux, Agnes
Dailey, Gina
Darzacq, Xavier
Heard, Edith
RNA polymerase II depletion from the inactive X chromosome territory is not mediated by physical compartmentalization
title RNA polymerase II depletion from the inactive X chromosome territory is not mediated by physical compartmentalization
title_full RNA polymerase II depletion from the inactive X chromosome territory is not mediated by physical compartmentalization
title_fullStr RNA polymerase II depletion from the inactive X chromosome territory is not mediated by physical compartmentalization
title_full_unstemmed RNA polymerase II depletion from the inactive X chromosome territory is not mediated by physical compartmentalization
title_short RNA polymerase II depletion from the inactive X chromosome territory is not mediated by physical compartmentalization
title_sort rna polymerase ii depletion from the inactive x chromosome territory is not mediated by physical compartmentalization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10442225/
https://www.ncbi.nlm.nih.gov/pubmed/37291424
http://dx.doi.org/10.1038/s41594-023-01008-5
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