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Chromosome Y pericentric heterochromatin is a primary target of HSF1 in male cells

The heat shock factor 1 (HSF1)-dependent transcriptional activation of human pericentric heterochromatin in heat-shocked cells is the most striking example of transcriptional activation of heterochromatin. Until now, pericentric heterochromatin of chromosome 9 has been identified as the primary targ...

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Autores principales: Penin, Jessica, Dufour, Solenne, Faure, Virginie, Fritah, Sabrina, Seigneurin-Berny, Daphné, Col, Edwige, Verdel, André, Vourc’h, Claire
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889540/
https://www.ncbi.nlm.nih.gov/pubmed/33547955
http://dx.doi.org/10.1007/s00412-021-00751-2
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author Penin, Jessica
Dufour, Solenne
Faure, Virginie
Fritah, Sabrina
Seigneurin-Berny, Daphné
Col, Edwige
Verdel, André
Vourc’h, Claire
author_facet Penin, Jessica
Dufour, Solenne
Faure, Virginie
Fritah, Sabrina
Seigneurin-Berny, Daphné
Col, Edwige
Verdel, André
Vourc’h, Claire
author_sort Penin, Jessica
collection PubMed
description The heat shock factor 1 (HSF1)-dependent transcriptional activation of human pericentric heterochromatin in heat-shocked cells is the most striking example of transcriptional activation of heterochromatin. Until now, pericentric heterochromatin of chromosome 9 has been identified as the primary target of HSF1, in both normal and tumor heat-shocked cells. Transcriptional awakening of this large genomic region results in the nuclear accumulation of satellite III (SATIII) noncoding RNAs (ncRNAs) and the formation in cis of specific structures known as nuclear stress bodies (nSBs). Here, we show that, in four different male cell lines, including primary human fibroblasts and amniocytes, pericentric heterochromatin of chromosome Y can also serve as a unique primary site of HSF1-dependent heterochromatin transcriptional activation, production of SATIII ncRNA, and nucleation of nuclear stress bodies (nSBs) upon heat shock. Our observation suggests that the chromosomal origin of SATIII transcripts in cells submitted to heat shock is not a determinant factor as such, but that transcription of SATIII repetitive units or the SATIII ncRNA molecules is the critical element of HSF1-dependent transcription activation of constitutive heterochromatin. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00412-021-00751-2.
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spelling pubmed-78895402021-03-03 Chromosome Y pericentric heterochromatin is a primary target of HSF1 in male cells Penin, Jessica Dufour, Solenne Faure, Virginie Fritah, Sabrina Seigneurin-Berny, Daphné Col, Edwige Verdel, André Vourc’h, Claire Chromosoma Original Article The heat shock factor 1 (HSF1)-dependent transcriptional activation of human pericentric heterochromatin in heat-shocked cells is the most striking example of transcriptional activation of heterochromatin. Until now, pericentric heterochromatin of chromosome 9 has been identified as the primary target of HSF1, in both normal and tumor heat-shocked cells. Transcriptional awakening of this large genomic region results in the nuclear accumulation of satellite III (SATIII) noncoding RNAs (ncRNAs) and the formation in cis of specific structures known as nuclear stress bodies (nSBs). Here, we show that, in four different male cell lines, including primary human fibroblasts and amniocytes, pericentric heterochromatin of chromosome Y can also serve as a unique primary site of HSF1-dependent heterochromatin transcriptional activation, production of SATIII ncRNA, and nucleation of nuclear stress bodies (nSBs) upon heat shock. Our observation suggests that the chromosomal origin of SATIII transcripts in cells submitted to heat shock is not a determinant factor as such, but that transcription of SATIII repetitive units or the SATIII ncRNA molecules is the critical element of HSF1-dependent transcription activation of constitutive heterochromatin. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00412-021-00751-2. Springer Berlin Heidelberg 2021-02-06 2021 /pmc/articles/PMC7889540/ /pubmed/33547955 http://dx.doi.org/10.1007/s00412-021-00751-2 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Penin, Jessica
Dufour, Solenne
Faure, Virginie
Fritah, Sabrina
Seigneurin-Berny, Daphné
Col, Edwige
Verdel, André
Vourc’h, Claire
Chromosome Y pericentric heterochromatin is a primary target of HSF1 in male cells
title Chromosome Y pericentric heterochromatin is a primary target of HSF1 in male cells
title_full Chromosome Y pericentric heterochromatin is a primary target of HSF1 in male cells
title_fullStr Chromosome Y pericentric heterochromatin is a primary target of HSF1 in male cells
title_full_unstemmed Chromosome Y pericentric heterochromatin is a primary target of HSF1 in male cells
title_short Chromosome Y pericentric heterochromatin is a primary target of HSF1 in male cells
title_sort chromosome y pericentric heterochromatin is a primary target of hsf1 in male cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889540/
https://www.ncbi.nlm.nih.gov/pubmed/33547955
http://dx.doi.org/10.1007/s00412-021-00751-2
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