BRCA1-dependent and independent functions of BARD1

被引:24
作者
Irminger-Finger, I [1 ]
Leung, WC
机构
[1] Univ Geneva, Dept Geriatr, Louis Jeantet Lab Aging Res, Geneva, Switzerland
[2] Tulane Univ, Sch Med, Dept Pathol & Lab Med, Tulane Canc Ctr, New Orleans, LA 70112 USA
关键词
RING finger; ankyrin repeat; BRCT domain; ubiquitination;
D O I
10.1016/S1357-2725(01)00161-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Breast cancer susceptibility gene 1 (BRCA1)-associated RING domain (BARD1) was discovered as a protein interacting with the RING domain of BRCA1. It is structurally homologous to BRCA1 with which it shares the conserved RING finger and BRCT domains. BARD 1 is strongly expressed in spleen and testis, correlated with the expression of BRCA1. Co-localization of BARD1 with BRCA1 and other repair proteins indicate a function in DNA repair. A potential role of BARD1-BRCA1 complexes in ubiquitination of RNA Pol II, and the interaction of BARD1 with polyadenylation factor CstF-50, thus inhibiting mRNA processing, provide mechanisms for tumor suppression. BRCA1-independent functions of BARD1 were first noted by its inordinate expression in hormonally regulated uterine tissue. BARD1 repression lead to a premalignant phenotype in mammary gland epithelial cells. The interaction of BARD1 with NF-kappaB, suggests modulation of transcriptional activity independent of BRCA1. Elevated BARD 1 expression in apoptotic tumor cells was found associated with anti-BARD 1 immune response thus leading to new therapeutic approaches. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:582 / 587
页数:6
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