A mutation in a thioredoxin reductase homolog suppresses p53-induced growth inhibition in the fission yeast Schizosaccharomyces pombe

被引:63
作者
Casso, D
Beach, D
机构
[1] COLD SPRING HARBOR LAB,HOWARD HUGHES MED INST,COLD SPRING HARBOR,NY 11724
[2] SUNY STONY BROOK,GRAD PROGRAM MOL & CELLULAR BIOL,STONY BROOK,NY 11794
来源
MOLECULAR & GENERAL GENETICS | 1996年 / 252卷 / 05期
关键词
p53; Schizosaccharomyces pombe; thioredoxin reductase; redox state; transcriptional reporter;
D O I
10.1007/s004380050259
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
A strong growth inhibition is observed when the human p53 tumor suppressor gene product is expressed in the fission yeast Schizosaccharomyces pombe. This growth inhibition is specific for wild-type p53; mutant alleles of p53 derived from human tumors show a greatly decreased ability to inhibit growth. These data suggest that there may be a p53-responsive pathway in S. pombe. To identify elements in this pathway genetically, we isolated a mutant yeast strain in which the growth inhibitory activity of p53 is largely suppressed. In addition, the activity of p53 as a transcription factor is also decreased in this strain. The suppression of p53 activity is not due to a decrease in p53 expression or a failure of p53 to localize to the nucleus. This p53 suppressor mutation is in a novel S. pombe gene with homology to thioredoxin reductase genes, and has been named trr1. Strains with a mutation of, or deletion in, trr1 are sensitive to oxidizing agents, suggesting that the trr1 suppressor mutation causes partial loss of trr1 function. Since oxidizing agents are able to suppress p53 activity in vitro, this trr1 mutation may affect the activity of p53 in fission yeast by increasing the oxidation state of the tumor suppressor.
引用
收藏
页码:518 / 529
页数:12
相关论文
共 69 条
[1]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[2]   MDM2 EXPRESSION IS INDUCED BY WILD TYPE-P53 ACTIVITY [J].
BARAK, Y ;
JUVEN, T ;
HAFFNER, R ;
OREN, M .
EMBO JOURNAL, 1993, 12 (02) :461-468
[3]   A PROTEOLYTIC FRAGMENT FROM THE CENTRAL REGION OF P53 HAS MARKED SEQUENCE-SPECIFIC DNA-BINDING ACTIVITY WHEN GENERATED FROM WILD-TYPE BUT NOT FROM ONCOGENIC MUTANT P53-PROTEIN [J].
BARGONETTI, J ;
MANFREDI, JJ ;
CHEN, XB ;
MARSHAK, DR ;
PRIVES, C .
GENES & DEVELOPMENT, 1993, 7 (12B) :2565-2574
[4]   RAN1+ CONTROLS THE TRANSITION FROM MITOTIC DIVISION TO MEIOSIS IN FISSION YEAST [J].
BEACH, D ;
RODGERS, L ;
GOULD, J .
CURRENT GENETICS, 1985, 10 (04) :297-311
[5]   HUMAN-P53 INHIBITS GROWTH IN SCHIZOSACCHAROMYCES-POMBE [J].
BISCHOFF, JR ;
CASSO, D ;
BEACH, D .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (04) :1405-1411
[6]  
BISCHOFF JR, 1991, ORIGINS OF HUMAN CANCER, P51
[7]   INTERACTION BETWEEN CDC13+ AND CDC2+ IN THE CONTROL OF MITOSIS IN FISSION YEAST - DISSOCIATION OF THE G1-ROLE AND G2-ROLE OF THE CDC2+ PROTEIN-KINASE [J].
BOOHER, R ;
BEACH, D .
EMBO JOURNAL, 1987, 6 (11) :3441-3447
[8]   THE FISSION YEAST CDC2 CDC13 SUC1 PROTEIN-KINASE - REGULATION OF CATALYTIC ACTIVITY AND NUCLEAR-LOCALIZATION [J].
BOOHER, RN ;
ALFA, CE ;
HYAMS, JS ;
BEACH, DH .
CELL, 1989, 58 (03) :485-497
[9]   P53-DEPENDENT APOPTOSIS IN THE ABSENCE OF TRANSCRIPTIONAL ACTIVATION OF P53-TARGET GENES [J].
CAELLES, C ;
HELMBERG, A ;
KARIN, M .
NATURE, 1994, 370 (6486) :220-223
[10]   CLONING AND SEQUENCING OF THIOL-SPECIFIC ANTIOXIDANT FROM MAMMALIAN BRAIN - ALKYL HYDROPEROXIDE REDUCTASE AND THIOL-SPECIFIC ANTIOXIDANT DEFINE A LARGE FAMILY OF ANTIOXIDANT ENZYMES [J].
CHAE, HZ ;
ROBISON, K ;
POOLE, LB ;
CHURCH, G ;
STORZ, G ;
RHEE, SG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (15) :7017-7021