CHD4 in the DNA-damage response and cell cycle progression: not so NuRDy now

التفاصيل البيبلوغرافية
العنوان: CHD4 in the DNA-damage response and cell cycle progression: not so NuRDy now
المؤلفون: Aoife O'Shaughnessy, Brian Hendrich
المصدر: Biochemical Society Transactions
سنة النشر: 2013
مصطلحات موضوعية: PARP, poly(ADP-ribose) polymerase, ATR, ataxia telangiectasia- and Rad3-related, HDAC, histone deacetylase, medicine.disease_cause, Biochemistry, Autoantigens, Biochemical Society Annual Symposium No. 80, PHD, plant homeodomain, 0302 clinical medicine, Neoplasms, Transcriptional regulation, Genetics, chromodomain helicase DNA-binding 4 (CHD4), 0303 health sciences, ATM, ataxia telangiectasia mutated, Cell Cycle, Cell cycle, RNF, RING finger protein, Cell biology, Nucleosomes, MTA, metastasis-associated protein, 030220 oncology & carcinogenesis, MDC1, mediator of DNA damage checkpoint 1, Mi-2 Nucleosome Remodeling and Deacetylase Complex, S1, DNA damage, S7, DNA repair, BRCA1, breast cancer early-onset 1, CHD, chromodomain-helicase-DNA-binding, Biology, Models, Biological, 03 medical and health sciences, medicine, Nucleosome, Animals, Humans, 030304 developmental biology, nucleosome remodelling and deacetylation (NuRD), NuRD, nucleosome remodelling and deacetylation, Chromatin Assembly and Disassembly, Mi-2/NuRD complex, EP300, E1A binding protein p300, Acetylation, γH2AX, phosphorylated histone H2AX, DDR, DNA-damage response, chromatin, CHD4, Carcinogenesis
الوصف: 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 G2. Furthermore, as part of NuRD, it participates in regulating acetylation levels of p53, thereby indirectly regulating the G1/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.
تدمد: 1470-8752
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60576676b73ee2e64020e955323475cdTest
https://pubmed.ncbi.nlm.nih.gov/23697937Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....60576676b73ee2e64020e955323475cd
قاعدة البيانات: OpenAIRE