THE UV RESPONSE INVOLVING THE RAS SIGNALING PATHWAY AND AP-1 TRANSCRIPTION FACTORS IS CONSERVED BETWEEN YEAST AND MAMMALS

被引:213
作者
ENGELBERG, D [1 ]
KLEIN, C [1 ]
MARTINETTO, H [1 ]
STRUHL, K [1 ]
KARIN, M [1 ]
机构
[1] HARVARD UNIV,SCH MED,DEPT BIOL CHEM & MOLEC PHARMACOL,BOSTON,MA 02115
关键词
D O I
10.1016/0092-8674(94)90153-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
UV irradiation of mammalian cells activates AP-1 through a Ras-dependent pathway, independently of DNA damage. We show that the yeast S. cerevisiae has a remarkably similar UV response involving the AP-1 factor Gcn4, which is distinct from the DNA damage response. Transcriptional activation of HIS3 and HIS4 by Gcn4 is triggered by UV irradiation in a Ras-dependent fashion. Moreover, resistance of yeast to UV irradiation is correlated with the level of Ras activity and Gcn4 function. Like mammalian cells in which activated Ras leads to increased c-Jun synthesis and phosphorylation, the effects in yeast involve increased translation of GCN4 mRNA and a posttranslational event. However, this effect on GCN4 translation is different from the response to amino acid or purine starvation. Therefore, a UV signaling pathway involving Ras and AP-1 is an ancient and universal mechanism involved in protection against damage to cellular components other than DNA.
引用
收藏
页码:381 / 390
页数:10
相关论文
共 72 条
[1]
THE ROLE OF JUN, FOS AND THE AP-1 COMPLEX IN CELL-PROLIFERATION AND TRANSFORMATION [J].
ANGEL, P ;
KARIN, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1072 (2-3) :129-157
[2]
ONCOGENE JUN ENCODES A SEQUENCE-SPECIFIC TRANS-ACTIVATOR SIMILAR TO AP-1 [J].
ANGEL, P ;
ALLEGRETTO, EA ;
OKINO, ST ;
HATTORI, K ;
BOYLE, WJ ;
HUNTER, T ;
KARIN, M .
NATURE, 1988, 332 (6160) :166-171
[3]
GCN4 PROTEIN, A POSITIVE TRANSCRIPTION FACTOR IN YEAST, BINDS GENERAL CONTROL PROMOTERS AT ALL 5' TGACTC 3' SEQUENCES [J].
ARNDT, K ;
FINK, GR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (22) :8516-8520
[4]
RAS GENES [J].
BARBACID, M .
ANNUAL REVIEW OF BIOCHEMISTRY, 1987, 56 :779-827
[5]
HA-RAS AUGMENTS C-JUN ACTIVITY AND STIMULATES PHOSPHORYLATION OF ITS ACTIVATION DOMAIN [J].
BINETRUY, B ;
SMEAL, T ;
KARIN, M .
NATURE, 1991, 351 (6322) :122-127
[6]
HUMAN PROTOONCOGENE C-JUN ENCODES A DNA-BINDING PROTEIN WITH STRUCTURAL AND FUNCTIONAL-PROPERTIES OF TRANSCRIPTION FACTOR AP-1 [J].
BOHMANN, D ;
BOS, TJ ;
ADMON, A ;
NISHIMURA, T ;
VOGT, PK ;
TJIAN, R .
SCIENCE, 1987, 238 (4832) :1386-1392
[7]
BOS JL, 1989, CANCER RES, V49, P4682
[8]
Broach J R, 1990, Adv Cancer Res, V54, P79, DOI 10.1016/S0065-230X(08)60809-X
[9]
INSULIN STIMULATION OF GENE-EXPRESSION MEDIATED BY P21RAS ACTIVATION [J].
BURGERING, BMT ;
MEDEMA, RH ;
MAASSEN, JA ;
VANDEWETERING, ML ;
VANDEREB, AJ ;
MCCORMICK, F ;
BOS, JL .
EMBO JOURNAL, 1991, 10 (05) :1103-1109
[10]
BUSCHER M, 1988, ONCOGENE, V3, P301