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CHD4 in the DNA-damage response and cell cycle progression: not so NuRDy now
The CHD4 (chromodomain-helicase-DNA-binding 4) (or Mi-2β) protein is a founding component of the NuRD (nucleosome remodelling and deacetylation) complex. NuRD has long been known to function in transcriptional regulation, and is conserved throughout the animal and plant kingdoms. In recent years, ev...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3685327/ https://www.ncbi.nlm.nih.gov/pubmed/23697937 http://dx.doi.org/10.1042/BST20130027 |
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author | O’Shaughnessy, Aoife Hendrich, Brian |
author_facet | O’Shaughnessy, Aoife Hendrich, Brian |
author_sort | O’Shaughnessy, Aoife |
collection | PubMed |
description | The CHD4 (chromodomain-helicase-DNA-binding 4) (or Mi-2β) protein is a founding component of the NuRD (nucleosome remodelling and deacetylation) complex. NuRD has long been known to function in transcriptional regulation, and is conserved throughout the animal and plant kingdoms. In recent years, evidence has steadily accumulated indicating that CHD4 can both function outside of the NuRD complex and also play important roles in cellular processes other than transcriptional regulation. A number of loss-of-function studies have identified important roles for CHD4 in the DNA-damage response and in cell cycle progression through S-phase and into G(2). Furthermore, as part of NuRD, it participates in regulating acetylation levels of p53, thereby indirectly regulating the G(1)/S cell cycle checkpoint. Although CHD4 has a somewhat complicated relationship with the cell cycle, recent evidence indicates that CHD4 may exert some tumour-suppressor functions in human carcinogenesis. CHD4 is a defining member of the NuRD complex, but evidence is accumulating that CHD4 also plays important NuRD-independent roles in the DNA-damage response and cell cycle progression, as well as in transcriptional regulation. |
format | Online Article Text |
id | pubmed-3685327 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-36853272013-06-24 CHD4 in the DNA-damage response and cell cycle progression: not so NuRDy now O’Shaughnessy, Aoife Hendrich, Brian Biochem Soc Trans Biochemical Society Annual Symposium No. 80 The CHD4 (chromodomain-helicase-DNA-binding 4) (or Mi-2β) protein is a founding component of the NuRD (nucleosome remodelling and deacetylation) complex. NuRD has long been known to function in transcriptional regulation, and is conserved throughout the animal and plant kingdoms. In recent years, evidence has steadily accumulated indicating that CHD4 can both function outside of the NuRD complex and also play important roles in cellular processes other than transcriptional regulation. A number of loss-of-function studies have identified important roles for CHD4 in the DNA-damage response and in cell cycle progression through S-phase and into G(2). Furthermore, as part of NuRD, it participates in regulating acetylation levels of p53, thereby indirectly regulating the G(1)/S cell cycle checkpoint. Although CHD4 has a somewhat complicated relationship with the cell cycle, recent evidence indicates that CHD4 may exert some tumour-suppressor functions in human carcinogenesis. CHD4 is a defining member of the NuRD complex, but evidence is accumulating that CHD4 also plays important NuRD-independent roles in the DNA-damage response and cell cycle progression, as well as in transcriptional regulation. Portland Press Ltd. 2013-05-23 2013-06-01 /pmc/articles/PMC3685327/ /pubmed/23697937 http://dx.doi.org/10.1042/BST20130027 Text en © 2013 The author(s) has paid for this article to be freely available under the terms of the Creative Commons Attribution Licence (CC-BY)(http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biochemical Society Annual Symposium No. 80 O’Shaughnessy, Aoife Hendrich, Brian CHD4 in the DNA-damage response and cell cycle progression: not so NuRDy now |
title | CHD4 in the DNA-damage response and cell cycle progression: not so NuRDy now |
title_full | CHD4 in the DNA-damage response and cell cycle progression: not so NuRDy now |
title_fullStr | CHD4 in the DNA-damage response and cell cycle progression: not so NuRDy now |
title_full_unstemmed | CHD4 in the DNA-damage response and cell cycle progression: not so NuRDy now |
title_short | CHD4 in the DNA-damage response and cell cycle progression: not so NuRDy now |
title_sort | chd4 in the dna-damage response and cell cycle progression: not so nurdy now |
topic | Biochemical Society Annual Symposium No. 80 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3685327/ https://www.ncbi.nlm.nih.gov/pubmed/23697937 http://dx.doi.org/10.1042/BST20130027 |
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