IDENTIFICATION OF A GENE LOCATED AT CHROMOSOME-5Q21 THAT IS MUTATED IN COLORECTAL CANCERS

被引:683
作者
KINZLER, KW
NILBERT, MC
VOGELSTEIN, B
BRYAN, TM
LEVY, DB
SMITH, KJ
PREISINGER, AC
HAMILTON, SR
HEDGE, P
MARKHAM, A
CARLSON, M
JOSLYN, G
GRODEN, J
WHITE, R
MIKI, Y
MIYOSHI, Y
NISHISHO, I
NAKAMURA, Y
机构
[1] JOHNS HOPKINS ONCOL CTR,MOLEC GENET LAB,BALTIMORE,MD 21231
[2] JOHNS HOPKINS UNIV HOSP,CTR ONCOL,BALTIMORE,MD 21205
[3] JOHNS HOPKINS UNIV HOSP,DEPT PATHOL,BALTIMORE,MD 21205
[4] UNIV UTAH,HOWARD HUGHES MED INST,SALT LAKE CITY,UT 84132
[5] JAPANESE FDN CANC RES,INST CANC,TOKYO 170,JAPAN
关键词
D O I
10.1126/science.1848370
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Recent studies have suggested the existence of a tumor suppressor gene located at chromosome region 5q21. DNA probes from this region were used to study a panel of sporadic colorectal carcinomas. One of these probes, cosmid 5.71, detected a somatically rearranged restriction fragment in the DNA from a single tumor. Further analysis of the 5.71 cosmid revealed two regions that were highly conserved in rodent DNA. These sequences were used to identify a gene, MCC (mutated in colorectal cancer), which encodes an 829-amino acid protein with a short region of similarity to the G protein-coupled m3 muscarinic acetylcholine receptor. The rearrangement in the tumor disrupted the coding region of the MCC gene. Moreover, two colorectal tumors were found with somatically acquired point mutations in MCC that resulted in amino acid substitutions. MCC is thus a candidate for the putative colorectal tumor suppressor gene located at 5q21. Further studies will be required to determine whether the gene is mutated in other sporadic tumors or in the germ line of patients with an inherited predisposition to colonic tumorigenesis.
引用
收藏
页码:1366 / 1370
页数:5
相关论文
共 43 条
  • [1] ASHTONRICKARDT PG, 1989, ONCOGENE, V4, P1169
  • [2] SUPPRESSION OF HUMAN COLORECTAL-CARCINOMA CELL-GROWTH BY WILD-TYPE-P53
    BAKER, SJ
    MARKOWITZ, S
    FEARON, ER
    WILLSON, JKV
    VOGELSTEIN, B
    [J]. SCIENCE, 1990, 249 (4971) : 912 - 915
  • [3] BAKER SJ, 1990, CANCER RES, V50, P7717
  • [4] CHROMOSOME-17 DELETIONS AND P53 GENE-MUTATIONS IN COLORECTAL CARCINOMAS
    BAKER, SJ
    FEARON, ER
    NIGRO, JM
    HAMILTON, SR
    PREISINGER, AC
    JESSUP, JM
    VANTUINEN, P
    LEDBETTER, DH
    BARKER, DF
    NAKAMURA, Y
    WHITE, R
    VOGELSTEIN, B
    [J]. SCIENCE, 1989, 244 (4901) : 217 - 221
  • [5] THE NF1 LOCUS ENCODES A PROTEIN FUNCTIONALLY RELATED TO MAMMALIAN GAP AND YEAST IRA PROTEINS
    BALLESTER, R
    MARCHUK, D
    BOGUSKI, M
    SAULINO, A
    LETCHER, R
    WIGLER, M
    COLLINS, F
    [J]. CELL, 1990, 63 (04) : 851 - 859
  • [6] THE MOLECULAR-GENETICS OF CANCER
    BISHOP, JM
    [J]. SCIENCE, 1987, 235 (4786) : 305 - 311
  • [7] LOCALIZATION OF THE GENE FOR FAMILIAL ADENOMATOUS POLYPOSIS ON CHROMOSOME-5
    BODMER, WF
    BAILEY, CJ
    BODMER, J
    BUSSEY, HJR
    ELLIS, A
    GORMAN, P
    LUCIBELLO, FC
    MURDAY, VA
    RIDER, SH
    SCAMBLER, P
    SHEER, D
    SOLOMON, E
    SPURR, NK
    [J]. NATURE, 1987, 328 (6131) : 614 - 616
  • [8] PREVALENCE OF RAS GENE-MUTATIONS IN HUMAN COLORECTAL CANCERS
    BOS, JL
    FEARON, ER
    HAMILTON, SR
    VERLAANDEVRIES, M
    VANBOOM, JH
    VANDEREB, AJ
    VOGELSTEIN, B
    [J]. NATURE, 1987, 327 (6120) : 293 - 297
  • [9] THE GTPASE SUPERFAMILY - A CONSERVED SWITCH FOR DIVERSE CELL FUNCTIONS
    BOURNE, HR
    SANDERS, DA
    MCCORMICK, F
    [J]. NATURE, 1990, 348 (6297) : 125 - 132
  • [10] CHARNEAU J, 1990, GASTROEN CLIN BIOL, V14, P153