LET-60, A GENE THAT SPECIFIES CELL FATES DURING C-ELEGANS VULVAR INDUCTION, ENCODES A RAS PROTEIN

被引:345
作者
HAN, M
STERNBERG, PW
机构
[1] Howard Hughes Medical Institute Division of Biology, 156-29 California Institute of Technology Pasadena
关键词
D O I
10.1016/0092-8674(90)90495-Z
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
Genetic analysis previously suggested that the let-60 gene controls the switch between vulval and hypodermal cell fates during C. elegans vulval induction. We have cloned the let-60 gene, and shown that it encodes a gene product identical in 84% of its first 164 amino acids to ras gene products from other vertebrate and invertebrate species. This conservation suggests that the let-60 product contains all the biochemical functions of ras proteins. Extrachromosomal arrays of let-60 ras DNA cause cell-type misspecification (extra vulval fates) phenotypically opposite to that caused by let-60 ras loss-of-function mutations (no vulval fates), and suppress the vulvaless phenotype of mutations in two other genes necessary for vulval induction. Thus, the level and pattern of let-60 ras expression may be under strict regulation; increase in let-60 ras activity bypasses or reduces the need for upstream genes in the vulval induction pathway. © 1990.
引用
收藏
页码:921 / 931
页数:11
相关论文
共 56 条
[1]  
Ausubel F, 1988, CURRENT PROTOCOLS MO
[2]   RAS GENES [J].
BARBACID, M .
ANNUAL REVIEW OF BIOCHEMISTRY, 1987, 56 :779-827
[3]  
BARSTEAD RJ, 1989, J BIOL CHEM, V264, P10177
[4]  
BRENNER S, 1974, GENETICS, V77, P71
[5]   THE SACCHAROMYCES-CEREVISIAE CDC25 GENE-PRODUCT REGULATES THE RAS/ADENYLATE CYCLASE PATHWAY [J].
BROEK, D ;
TODA, T ;
MICHAELI, T ;
LEVIN, L ;
BIRCHMEIER, C ;
ZOLLER, M ;
POWERS, S ;
WIGLER, M .
CELL, 1987, 48 (05) :789-799
[6]   MECHANISM OF ACTIVATION OF AN N-RAS GENE IN THE HUMAN FIBRO-SARCOMA CELL-LINE HT1080 [J].
BROWN, R ;
MARSHALL, CJ ;
PENNIE, SG ;
HALL, A .
EMBO JOURNAL, 1984, 3 (06) :1321-1326
[7]   MYRISTIC ACID IS ATTACHED TO THE TRANSFORMING PROTEIN OF ROUS-SARCOMA VIRUS DURING OR IMMEDIATELY AFTER SYNTHESIS AND IS PRESENT IN BOTH SOLUBLE AND MEMBRANE-BOUND FORMS OF THE PROTEIN [J].
BUSS, JE ;
KAMPS, MP ;
SEFTON, BM .
MOLECULAR AND CELLULAR BIOLOGY, 1984, 4 (12) :2697-2704
[8]   TUMORIGENIC TRANSFORMATION OF MAMMALIAN-CELLS INDUCED BY A NORMAL HUMAN-GENE HOMOLOGOUS TO THE ONCOGENE OF HARVEY MURINE SARCOMA-VIRUS [J].
CHANG, EH ;
FURTH, ME ;
SCOLNICK, EM ;
LOWY, DR .
NATURE, 1982, 297 (5866) :479-483
[9]   POSTTRANSLATIONAL PROCESSING OF P21 RAS PROTEINS INVOLVES PALMITYLATION OF THE C-TERMINAL TETRAPEPTIDE CONTAINING CYSTEINE-186 [J].
CHEN, ZQ ;
ULSH, LS ;
DUBOIS, G ;
SHIH, TY .
JOURNAL OF VIROLOGY, 1985, 56 (02) :607-612
[10]  
CLARK DV, 1988, GENETICS, V119, P345