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
相关论文
共 51 条
  • [41] MLH1, PMS1, AND MSH2 INTERACTIONS DURING THE INITIATION OF DNA MISMATCH REPAIR IN YEAST
    PROLLA, TA
    PANG, QS
    ALANI, E
    KOLODNER, RD
    LISKAY, RM
    [J]. SCIENCE, 1994, 265 (5175) : 1091 - 1093
  • [42] Reitmair AH, 1996, CANCER RES, V56, P3842
  • [43] MSH2 DEFICIENT MICE ARE VIABLE AND SUSCEPTIBLE TO LYMPHOID TUMORS
    REITMAIR, AH
    SCHMITS, R
    EWEL, A
    BAPAT, B
    REDSTON, M
    MITRI, A
    WATERHOUSE, P
    MITTRUCKER, HW
    WAKEHAM, A
    LIU, B
    THOMASON, A
    GRIESSER, H
    GALLINGER, S
    BALLHAUSEN, WG
    FISHEL, R
    MAK, TW
    [J]. NATURE GENETICS, 1995, 11 (01) : 64 - 70
  • [44] Mutation of MSH3 in endometrial cancer and evidence for its functional role in heteroduplex repair
    Risinger, JI
    Umar, A
    Boyd, J
    Berchuck, A
    Kunkel, TA
    Barrett, JC
    [J]. NATURE GENETICS, 1996, 14 (01) : 102 - 105
  • [45] A HPMS2 MUTANT-CELL LINE IS DEFECTIVE IN STRAND-SPECIFIC MISMATCH REPAIR
    RISINGER, JI
    UMAR, A
    BARRETT, JC
    KUNKEL, TA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (31) : 18183 - 18186
  • [46] GENOMIC INSTABILITY IN REPEATED SEQUENCES IS AN EARLY SOMATIC EVENT IN COLORECTAL TUMORIGENESIS THAT PERSISTS AFTER TRANSFORMATION
    SHIBATA, D
    PEINADO, MA
    IONOV, Y
    MALKHOSYAN, S
    PERUCHO, M
    [J]. NATURE GENETICS, 1994, 6 (03) : 273 - 281
  • [47] Microsatellite instability in yeast: Dependence on repeat unit size and DNA mismatch repair genes
    Sia, EA
    Kokoska, RJ
    Dominska, M
    Greenwell, P
    Petes, TD
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (05) : 2851 - 2858
  • [48] MICE DEVELOP NORMALLY WITHOUT THE H1(0) LINKER HISTONE
    SIROTKIN, AM
    EDELMANN, W
    CHENG, GH
    KLEINSZANTO, A
    KUCHERLAPATI, R
    SKOULTCHI, AI
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (14) : 6434 - 6438
  • [49] THOMAS DC, 1991, J BIOL CHEM, V266, P3744
  • [50] THOMAS DC, 1995, METHODS COMPANION ME, P187