Mutation in the mismatch repair gene Msh6 causes cancer susceptibility

被引:313
作者
Edelmann, W
Yang, K
Umar, A
Heyer, J
Lau, K
Fan, KH
Liedtke, W
Cohen, PE
Kane, MF
Lipford, JR
Yu, NJ
Crouse, GF
Pollard, JW
Kunkel, T
Lipkin, M
Kolodner, R
Kucherlapati, R
机构
[1] YESHIVA UNIV ALBERT EINSTEIN COLL MED,DEPT MOL GENET,BRONX,NY 10461
[2] YESHIVA UNIV ALBERT EINSTEIN COLL MED,DEPT PATHOL,BRONX,NY 10461
[3] YESHIVA UNIV ALBERT EINSTEIN COLL MED,DEPT DEV & MOL BIOL,BRONX,NY 10461
[4] YESHIVA UNIV ALBERT EINSTEIN COLL MED,STRANG CANC RES LAB,BRONX,NY 10461
[5] NIEHS,NIH,RES TRIANGLE PK,NC 27709
[6] DANA FARBER CANC INST,BOSTON,MA 02115
[7] LUDWIG INST CANC RES,LA JOLLA,CA 92093
[8] EMORY UNIV,ATLANTA,GA 30322
关键词
D O I
10.1016/S0092-8674(00)80433-X
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
Mice carrying a null mutation in the mismatch repair gene Msh6 were generated by gene targeting. Cells that were homozygous for the mutation did not produce any detectable MSH6 protein, and extracts prepared from these cells were defective for repair of single nucleotide mismatches. Repair of 1, 2, and 4 nucleotide insertion/deletion mismatches was unaffected. Mice that were homozygous for the mutation had a reduced life span. The mice developed a spectrum of tumors, the most predominant of which were gastrointestinal tumors and B-as well as T-cell lymphomas. The tumors did not show any microsatellite instability. We conclude that MSH6 mutations, like those in some other members bf the family of mismatch repair genes, lead to cancer susceptibility, and germline mutations in this gene may be associated with a cancer predisposition syndrome that does not show microsatellite instability.
引用
收藏
页码:467 / 477
页数:11
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