Marsupial BRCA1: conserved regions in mammals and the potential effect of missense changes

被引:15
作者
Ramirez, CJ
Fleming, MA
Potter, JD
Ostrander, GK
Ostrander, EA
机构
[1] Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98109 USA
[2] Fred Hutchinson Canc Res Ctr, Div Human Biol, Seattle, WA 98109 USA
[3] Univ Washington, Dept Mol & Cellular Biol, Seattle, WA 98195 USA
[4] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Seattle, WA 98109 USA
[5] Johns Hopkins Univ, Dept Biol, Baltimore, MD 21218 USA
[6] Johns Hopkins Univ, Dept Comparat Med, Baltimore, MD 21218 USA
关键词
breast cancer; comparative analysis; exon; 11; gene evolution; missense; phylogenetics;
D O I
10.1038/sj.onc.1207292
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
More than half of the reported missense changes in the breast cancer susceptibility protein BRCA1 occur in exon 11, but none has been clearly identified as disease associated and only 28 are designated 'probable' neutral polymorphisms. Previously, in a comparison of sequences from 57 eutherian mammal species, we found seven 'highly conserved regions' between amino acids 282 and 1103, and identified 38 missense changes as likely to disrupt gene function. These conserved regions were also present in birds and amphibians and included only six of the mutations predicted to affect function. In this new analysis, we hypothesized that using 37 ancestral sequences derived from the 57 GenBank sequences and including eight marsupial sequences would allow us to identify regions unique to mammals and re. ne our predictions of disease-associated missense changes. We identified 13 conserved regions, three of which appear to be unique to mammals, and 21 likely disease-associated missense changes, 11 of which occur in conserved regions. Seven regions identified in this analysis, including the three found only in mammalian sequences, and nine missense changes predicted to affect function are in the putative STAT1-interaction domain, suggesting that the role of STAT1 in immune response is important to mammary function. The reduction in the number of missense changes predicted to be disease associated and the identification of conserved regions specific to mammals can facilitate the further study of the role of missense changes in BRCA1-associated breast cancers.
引用
收藏
页码:1780 / 1788
页数:9
相关论文
共 49 条
[1]   POLYMORPHIC DNA REGION ADJACENT TO THE 5'-END OF THE HUMAN INSULIN GENE [J].
BELL, GI ;
KARAM, JH ;
RUTTER, WJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (09) :5759-5763
[2]   Universal trees based on large combined protein sequence data sets [J].
Brown, JR ;
Douady, CJ ;
Italia, MJ ;
Marshall, WE ;
Stanhope, MJ .
NATURE GENETICS, 2001, 28 (03) :281-285
[3]   BRCA1 RING domain cancer-predisposing mutations - Structural consequences and effects on protein-protein interactions [J].
Brzovic, PS ;
Meza, JE ;
King, MC ;
Klevit, RE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (44) :41399-41406
[4]   SPONTANEOUS PROLIFERATIONS IN AUSTRALIAN MARSUPIALS - A SURVEY AND REVIEW .2. DASYURIDS AND BANDICOOTS [J].
CANFIELD, PJ ;
HARTLEY, WJ ;
REDDACLIFF, GL .
JOURNAL OF COMPARATIVE PATHOLOGY, 1990, 103 (02) :147-158
[5]   SPONTANEOUS PROLIFERATIONS IN AUSTRALIAN MARSUPIALS - A SURVEY AND REVIEW .1. MACROPODS, KOALAS, WOMBATS, POSSUMS AND GLIDERS [J].
CANFIELD, PJ ;
HARTLEY, WJ ;
REDDACLIFF, GL .
JOURNAL OF COMPARATIVE PATHOLOGY, 1990, 103 (02) :135-146
[6]  
Casey H W, 1979, Recent Results Cancer Res, V66, P129
[7]   MUTATIONS IN THE BRCA1 GENE IN FAMILIES WITH EARLY-ONSET BREAST AND OVARIAN-CANCER [J].
CASTILLA, LH ;
COUCH, FJ ;
ERDOS, MR ;
HOSKINS, KF ;
CALZONE, K ;
GARBER, JE ;
BOYD, J ;
LUBIN, MB ;
DESHANO, ML ;
BRODY, LC ;
COLLINS, FS ;
WEBER, BL .
NATURE GENETICS, 1994, 8 (04) :387-391
[8]   Comparative and functional analyses of LYL1 loci establish marsupial sequences as a model for phylogenetic footprinting [J].
Chapman, MA ;
Charchar, FJ ;
Kinston, S ;
Bird, CP ;
Grafham, D ;
Rogers, J ;
Grützner, F ;
Graves, JAM ;
Green, AR ;
Göttgens, B .
GENOMICS, 2003, 81 (03) :249-259
[9]   The nuclear localization sequences of the BRCA1 protein interact with the importin-alpha subunit of the nuclear transport signal receptor [J].
Chen, CF ;
Li, S ;
Chen, YM ;
Chen, PL ;
Sharp, ZD ;
Lee, WH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (51) :32863-32868
[10]   Comparison of BRCA1 polymorphisms, rare sequence variants and/or missense mutations in unaffected and breast/ovarian cancer populations [J].
Durocher, F ;
ShattuckEidens, D ;
McClure, M ;
Labrie, F ;
Skolnick, MH ;
Goldgar, DE ;
Simard, J .
HUMAN MOLECULAR GENETICS, 1996, 5 (06) :835-842