A truncated splice variant of human BARD1 that lacks the RING finger and ankyrin repeats

被引:23
作者
Tsuzuki, M
Wu, WW
Nishikawa, H
Hayami, R
Oyake, D
Yabuki, Y
Fukuda, M
Ohta, T
机构
[1] St Marianna Univ, Sch Med, Dept Surg, Div Breast & Endocrine Surg,Miyamae Ku, Kawasaki, Kanagawa 2168511, Japan
[2] St Marianna Univ, Sch Med, Dept Otorhinolaryngol, Kawasaki, Kanagawa 2168511, Japan
基金
日本学术振兴会;
关键词
BARD1; BRCA1; splicing variant; RING finger; ubiquitin;
D O I
10.1016/j.canlet.2005.03.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BARD1 is a crucial partner of the breast and ovarian tumor suppressor BRCA1 required for ubiquitin ligase activity and for reciprocal stabilization in cells. We report here an alternatively spliced human BARD1 mRNA variant (BARD1 Delta RIN) isolated from a HeLa cell cDNA library. It is characterized by deletion of exons 2-6 that encode most of the RING finger domain and the entire span of ankyrin repeats. Delta RIN transcript was detected in all breast cancer-cell lines studied although its protein expression level was low. Delta RIN does not interact with BRCA1, whereas it interacts with and colocalizes with CstF-50 to cytoplasmic dots. Hence, a deletion variant of BARD1 occurs in cells and may play a distinct role with CstF-50. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:108 / 116
页数:9
相关论文
共 23 条
[1]   Binding and recognition in the assembly of an active BRCA1 /BARD1 ubiquitin-ligase complex [J].
Brzovic, PS ;
Keeffe, JR ;
Nishikawa, H ;
Miyamoto, K ;
Fox, D ;
Fukuda, M ;
Ohta, T ;
Klevit, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (10) :5646-5651
[2]   BARD1 induces BRCA1 intranuclear foci formation by increasing RING-dependent BRCA1 nuclear import and inhibiting BRCA1 nuclear export [J].
Fabbro, M ;
Rodriguez, JA ;
Baer, R ;
Henderson, BR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (24) :21315-21324
[3]   Germline mutations of the BRICA1-associated ring domain (BARD1) gene in breast and breast/ovarian families negative for BRCA1 and BRCA2 alterations [J].
Ghimenti, C ;
Sensi, E ;
Presciuttini, S ;
Brunetti, IM ;
Conte, P ;
Bevilacqua, G ;
Caligo, MA .
GENES CHROMOSOMES & CANCER, 2002, 33 (03) :235-242
[4]   The RING heterodimer BRCA1-BARD1 is a ubiquitin ligase inactivated by a breast cancer-derived mutation [J].
Hashizume, R ;
Fukuda, M ;
Maeda, I ;
Nishikawa, H ;
Oyake, D ;
Yabuki, Y ;
Ogata, F ;
Ohta, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (18) :14537-14540
[5]   The ubiquitin system [J].
Hershko, A ;
Ciechanover, A .
ANNUAL REVIEW OF BIOCHEMISTRY, 1998, 67 :425-479
[6]   Nuclear-cytoplasmic translocation of BARD1 is linked to its apoptotic activity [J].
Jefford, CE ;
Feki, A ;
Harb, J ;
Krause, KH ;
Irminger-Finger, I .
ONCOGENE, 2004, 23 (20) :3509-3520
[7]   Functional communication between endogenous BRCA1 and its partner, BARD1, during Xenopus laevis development [J].
Joukov, V ;
Chen, J ;
Fox, EA ;
Green, JBA ;
Livingston, DM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (21) :12078-12083
[8]   Functional interaction of BRCA1-associated BARD1 with polyadenylation factor CstF-50 [J].
Kleiman, FE ;
Manley, JL .
SCIENCE, 1999, 285 (5433) :1576-1579
[9]   The BARD1-CstF-50 interaction links mRNA 3′ end formation to DNA damage and tumor suppression [J].
Kleiman, FE ;
Manley, JL .
CELL, 2001, 104 (05) :743-753
[10]   Loss of Bard1, the heterodimeric partner of the Brca1 tumor suppressor, results in early embryonic lethality and chromosomal instability [J].
McCarthy, EE ;
Celebi, JT ;
Baer, R ;
Ludwig, T .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (14) :5056-5063