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PMID: 10918303 Published · ppublish English Journal Article Review

Roles of BRCA1 and its interacting proteins.

Deng CX, Brodie SG

Abstract

Germline mutations of BRCA1 predispose women to breast and ovarian cancers. BRCA1 contains several functional domains that interact directly or indirectly with a variety of molecules, including tumor suppressors (p53, RB, BRCA2 and ATM), oncogenes (c-Myc, casein kinase II and E2F), DNA damage repair proteins (RAD50 and RAD51), cell-cycle regulators (cyclins and cyclin-dependent kinases), transcriptional activators and repressors (RNA polymerase II, RHA, histone deacetylase complex and CtIP) and others. Mounting evidence indicates that these physical associations are not artifacts; rather, BRCA1 is likely to serve as an important central component in multiple biological pathways that regulate cell-cycle progression, centrosome duplication, DNA damage repair, cell growth and apoptosis, and transcriptional activation and repression. This review examines our understanding of the significance of the interactions between BRCA1 and other proteins, through which BRCA1 maintains genome integrity and represses tumor formation. Published 2000 John Wiley & Sons, Inc.

MeSH Terms
BRCA1 Protein/chemistry,genetics,metabolism Binding Sites Breast Neoplasms/genetics Cell Cycle Cell Division Centrosome/metabolism DNA Damage DNA Repair Female Genes, p53 Humans Models, Biological Mutation Transcription, Genetic
Chemicals
BRCA1 Protein
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Deng C X
National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA. chuxiad@bdg10.niddk.nih.gov
Brodie S G
Article Info
Journal
BioEssays : news and reviews in molecular, cellular and developmental biology
Abbr.
Bioessays
ISSN
0265-9247
Published
2000-08-00
Pages
728-37
Language
English
Region
United States
NLM ID
8510851
Subset
IM
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