A genomewide screen in Saccharomyces cerevisiae for genes that suppress the accumulation of mutations

被引:225
作者
Huang, ME
Rio, AG
Nicolas, A
Kolodner, RD
机构
[1] Univ Calif San Diego, Sch Med, Ludwig Inst Canc Res, Dept Med, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Sch Med, Ctr Canc, La Jolla, CA 92093 USA
[3] Univ Rennes 1, CNRS, UMR 6061, F-35043 Rennes, France
[4] Inst Curie, CNRS, Sect Rech, UMR 144, F-75248 Paris, France
关键词
D O I
10.1073/pnas.2035018100
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
A genomewide screen of a collection of 4,847 yeast gene deletion mutants was carried out to identify the genes required for suppressing mutations in the CAN1 forward-mutation assay. The primary screens and subsequent analysis allowed (i) identification of 18 known mutator mutants, providing a solid means for checking the efficiency of the screen, and (it) identification of a number of genes not known previously to be involved in suppressing mutations. Among the previously uncharacterized mutation-suppressing genes were six genes of unknown function including four (CSM2, SHU2, SHU1, and YLR376c) encoding proteins that interact with each other and promote resistance to killing by methyl methanesulfonate, one gene (EGO) previously identified as suppressing Ty1 mobility and recombination between repeated sequences, and one gene (YLR154c) that was not associated with any known processes. In addition, five genes (TSA1, SOD1, LYS7, SKN7, and YAP1) implicated in the oxidative-stress responses were found to play a significant role in mutation suppression. Furthermore, TSA1, which encodes thioredoxin peroxidase, was found to strongly suppress gross chromosomal rearrangements. These results provide a global view of the nonessential genes involved in preventing mutagenesis. Study of such genes should provide useful clues in identification of human genes potentially involved in cancer predisposition and in understanding their mechanisms of action.
引用
收藏
页码:11529 / 11534
页数:6
相关论文
共 55 条
[51]   Interactions of Exo1p with components of MutLα in Saccharomyces cerevisiae [J].
Tran, PT ;
Simon, JA ;
Liskay, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (17) :9760-9765
[52]   A comprehensive analysis of protein-protein interactions in Saccharomyces cerevisiae [J].
Uetz, P ;
Giot, L ;
Cagney, G ;
Mansfield, TA ;
Judson, RS ;
Knight, JR ;
Lockshon, D ;
Narayan, V ;
Srinivasan, M ;
Pochart, P ;
Qureshi-Emili, A ;
Li, Y ;
Godwin, B ;
Conover, D ;
Kalbfleisch, T ;
Vijayadamodar, G ;
Yang, MJ ;
Johnston, M ;
Fields, S ;
Rothberg, JM .
NATURE, 2000, 403 (6770) :623-627
[53]   Genetic disorders associated with cancer predisposition and genomic instability [J].
Vessey, CJ ;
Norbury, CJ ;
Hickson, ID .
PROGRESS IN NUCLEIC ACID RESEARCH AND MOLECULAR BIOLOGY, VOL 63, 2000, 63 :189-221
[54]   Mutagenicity and repair of oxidative DNA damage: insights from studies using defined lesions [J].
Wang, D ;
Kreutzer, DA ;
Essigmann, JM .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1998, 400 (1-2) :99-115
[55]   DNA topoisomerases [J].
Wang, JC .
ANNUAL REVIEW OF BIOCHEMISTRY, 1996, 65 :635-692