Transcription-dependent cohesin repositioning rewires chromatin loops in cellular senescence
Senescence is a state of stable proliferative arrest. Here, the authors perform Hi-C analysis on oncogenic RAS-induced senescence in human fibroblasts and characterize the changes in the 3D genome folding associated with the senescence-specific gene expression profile, which are mediated in part thr...
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2020-11-01
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Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-020-19878-4 |
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doaj-cfcc6e6ce1f94a00978bd38e7e46977b2021-05-11T08:33:12ZengNature Publishing GroupNature Communications2041-17232020-11-0111111410.1038/s41467-020-19878-4Transcription-dependent cohesin repositioning rewires chromatin loops in cellular senescenceIoana Olan0Aled J. Parry1Stefan Schoenfelder2Masako Narita3Yoko Ito4Adelyne S. L. Chan5Guy St.C. Slater6Dóra Bihary7Masashige Bando8Katsuhiko Shirahige9Hiroshi Kimura10Shamith A. Samarajiwa11Peter Fraser12Masashi Narita13Cancer Research UK Cambridge Institute, University of CambridgeCancer Research UK Cambridge Institute, University of CambridgeEpigenetics Programme, The Babraham Institute, Babraham Research CampusCancer Research UK Cambridge Institute, University of CambridgeCancer Research UK Cambridge Institute, University of CambridgeCancer Research UK Cambridge Institute, University of CambridgeCancer Research UK Cambridge Institute, University of CambridgeMRC Cancer Unit, Hutchison/MRC Research Centre, University of Cambridge, Cambridge Biomedical CampusLaboratory of Genome Structure and Function, Institute of Molecular and Cellular Biosciences, The University of TokyoLaboratory of Genome Structure and Function, Institute of Molecular and Cellular Biosciences, The University of TokyoCell Biology Centre, Institute of Innovative Research, Tokyo Institute of TechnologyMRC Cancer Unit, Hutchison/MRC Research Centre, University of Cambridge, Cambridge Biomedical CampusNuclear Dynamics Programme, The Babraham Institute, Babraham Research CampusCancer Research UK Cambridge Institute, University of CambridgeSenescence is a state of stable proliferative arrest. Here, the authors perform Hi-C analysis on oncogenic RAS-induced senescence in human fibroblasts and characterize the changes in the 3D genome folding associated with the senescence-specific gene expression profile, which are mediated in part through cohesin redistribution on chromatin.https://doi.org/10.1038/s41467-020-19878-4 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ioana Olan Aled J. Parry Stefan Schoenfelder Masako Narita Yoko Ito Adelyne S. L. Chan Guy St.C. Slater Dóra Bihary Masashige Bando Katsuhiko Shirahige Hiroshi Kimura Shamith A. Samarajiwa Peter Fraser Masashi Narita |
spellingShingle |
Ioana Olan Aled J. Parry Stefan Schoenfelder Masako Narita Yoko Ito Adelyne S. L. Chan Guy St.C. Slater Dóra Bihary Masashige Bando Katsuhiko Shirahige Hiroshi Kimura Shamith A. Samarajiwa Peter Fraser Masashi Narita Transcription-dependent cohesin repositioning rewires chromatin loops in cellular senescence Nature Communications |
author_facet |
Ioana Olan Aled J. Parry Stefan Schoenfelder Masako Narita Yoko Ito Adelyne S. L. Chan Guy St.C. Slater Dóra Bihary Masashige Bando Katsuhiko Shirahige Hiroshi Kimura Shamith A. Samarajiwa Peter Fraser Masashi Narita |
author_sort |
Ioana Olan |
title |
Transcription-dependent cohesin repositioning rewires chromatin loops in cellular senescence |
title_short |
Transcription-dependent cohesin repositioning rewires chromatin loops in cellular senescence |
title_full |
Transcription-dependent cohesin repositioning rewires chromatin loops in cellular senescence |
title_fullStr |
Transcription-dependent cohesin repositioning rewires chromatin loops in cellular senescence |
title_full_unstemmed |
Transcription-dependent cohesin repositioning rewires chromatin loops in cellular senescence |
title_sort |
transcription-dependent cohesin repositioning rewires chromatin loops in cellular senescence |
publisher |
Nature Publishing Group |
series |
Nature Communications |
issn |
2041-1723 |
publishDate |
2020-11-01 |
description |
Senescence is a state of stable proliferative arrest. Here, the authors perform Hi-C analysis on oncogenic RAS-induced senescence in human fibroblasts and characterize the changes in the 3D genome folding associated with the senescence-specific gene expression profile, which are mediated in part through cohesin redistribution on chromatin. |
url |
https://doi.org/10.1038/s41467-020-19878-4 |
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