K-ras is an essential gene in the mouse with partial functional overlap with N-ras

被引:435
作者
Johnson, L
Greenbaum, D
Cichowski, K
Mercer, K
Murphy, E
Schmitt, E
Bronson, RT
Umanoff, H
Edelmann, W
Kucherlapati, R
Jacks, T
机构
[1] MIT,DEPT BIOL,CAMBRIDGE,MA 02139
[2] MIT,CTR CANC RES,HOWARD HUGHES MED INST,CAMBRIDGE,MA 02139
[3] UNIV CALIF SAN FRANCISCO,DEPT MED,SAN FRANCISCO,CA 94143
[4] TUFTS UNIV,SCH MED,DEPT PATHOL,BOSTON,MA 02111
[5] TUFTS UNIV,SCH VET MED,DEPT PATHOL,BOSTON,MA 02111
[6] YESHIVA UNIV ALBERT EINSTEIN COLL MED,DEPT MOL GENET,BRONX,NY 10461
关键词
K-ras; N-ras; oncogene; knockout mouse; embryogenesis; hematopoiesis;
D O I
10.1101/gad.11.19.2468
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mammalian ras genes are thought to be critical in the regulation of cellular proliferation and differentiation and are mutated in similar to 30% of all human tumors. However, N-ras and H-ras are nonessential for mouse development. To characterize the normal role of K-ras in growth and development, we have mutated it by gene targeting in the mouse. On an inbred genetic background, embryos homozygous for this mutation die between 12 and 14 days of gestation, with fetal liver defects and evidence of anemia. Thus, K-ras is the only member of the ras gene family essential for mouse embryogenesis. We have also investigated the effect of multiple mutations within the ras gene family. Most animals lacking N-ras function and heterozygous for the K-ras mutation exhibit abnormal hematopoietic development and die between days 10 and 12 of embryogenesis. Thus, partial functional overlap appears to occur within the ras gene family, but K-ras provides a unique and essential function.
引用
收藏
页码:2468 / 2481
页数:14
相关论文
共 56 条
  • [1] RAS GENES
    BARBACID, M
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1987, 56 : 779 - 827
  • [2] BOS JL, 1990, CANCER RES, V50, P1352
  • [3] GENETIC MECHANISMS IN TUMOR INITIATION AND PROGRESSION .10. THE RAS GENE FAMILY AND HUMAN CARCINOGENESIS
    BOS, JL
    [J]. MUTATION RESEARCH, 1988, 195 (03): : 255 - 271
  • [4] BOS JL, 1989, CANCER RES, V49, P4682
  • [5] THE GTPASE SUPERFAMILY - A CONSERVED SWITCH FOR DIVERSE CELL FUNCTIONS
    BOURNE, HR
    SANDERS, DA
    MCCORMICK, F
    [J]. NATURE, 1990, 348 (6297) : 125 - 132
  • [6] Bradley A., 1987, TERATOCARCINOMAS EMB, P113
  • [7] EFFECT OF A DOMINANT INHIBITORY HA-RAS MUTATION ON MITOGENIC SIGNAL TRANSDUCTION IN NIH 3T3 CELLS
    CAI, H
    SZEBERENYI, J
    COOPER, GM
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (10) : 5314 - 5323
  • [8] ACTIVATION OF KI-RAS 2 GENE IN HUMAN-COLON AND LUNG CARCINOMAS BY 2 DIFFERENT POINT MUTATIONS
    CAPON, DJ
    SEEBURG, PH
    MCGRATH, JP
    HAYFLICK, JS
    EDMAN, U
    LEVINSON, AD
    GOEDDEL, DV
    [J]. NATURE, 1983, 304 (5926) : 507 - 513
  • [9] EXPRESSION OF P21RAS IN NORMAL AND MALIGNANT HUMAN-TISSUES - LACK OF ASSOCIATION WITH PROLIFERATION AND MALIGNANCY
    CHESA, PG
    RETTIG, WJ
    MELAMED, MR
    OLD, LJ
    NIMAN, HL
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (10) : 3234 - 3238
  • [10] THE INS AND OUTS OF RAF KINASES
    DAUM, G
    EISENMANNTAPPE, I
    FRIES, HW
    TROPPMAIR, J
    RAPP, UR
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1994, 19 (11) : 474 - 480