HIM1, a new yeast Saccharomyces cerevisiae gene playing a role in control of spontaneous and induced mutagenesis

被引:11
作者
Kelberg, EP [1 ]
Kovaltsova, SV [1 ]
Alekseev, SY [1 ]
Fedorova, IV [1 ]
Gracheva, LM [1 ]
Evstukhina, TA [1 ]
Korolev, VG [1 ]
机构
[1] Russian Acad Sci, Petersburg Nucl Phys Inst, Div Mol & Radiat Biophys, Lab Eukaryote Genet, Gatchina 188350, Leningrad Distr, Russia
关键词
yeast; him1; mutant; DNA repair; mutagenesis;
D O I
10.1016/j.mrfmmm.2005.03.003
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We have identified a new Saccharomyces cerevisiae gene, HIM1, mapped on the right arm of the chromosome IV (ORF YDR317w), mutations in which led to an increase in spontaneous mutation rate and elevated the frequencies of mutations, induced by UV-light, nitrous acid, ethylmethane sulfonate and methylmethane sulfonate. At the same time, him1 mutation did not result in the increase of the sensitivity to the lethal action of these DNA-damaging agents. We tested the induced mutagenesis in double mutants carrying him] mutation and mutations in other repair genes: apn1, blocking base excision repair; rad2, rev3, and rad54, blocking three principal DNA repair pathways; pms1, blocking mismatch repair; hsm2 and hsm3 mutations, which lead to a mutator effect. Epistatic analysis showed a synergistic interaction of him] with pms1, apn1, and rad2 mutations, and epistasis with the rev3, the rad54, the hsm2, and the hsm3. To elucidate the role of the HIM1 in control of spontaneous mutagenesis, we checked the repair of DNA mispaired bases in the him1 mutant and discovered that it was not altered in comparison to the wild-type strain. In our opinion, our results suggest that HIM1 gene participates in the control of processing of mutational intermediates appearing during error-prone bypass of DNA damage. (C) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:64 / 78
页数:15
相关论文
共 46 条
[1]   HSM2 (HMO1) gene participates in mutagenesis control in yeast Saccharomyces cerevisiae [J].
Alekseev, SY ;
Kovaltsova, SV ;
Fedorova, IV ;
Gracheva, LM ;
Evstukhina, TA ;
Peshekhonov, VT ;
Korolev, VG .
DNA REPAIR, 2002, 1 (04) :287-297
[2]   Regulation of alternative replication bypass pathways at stalled replication forks and its effects on genome stability: a yeast model [J].
Barbour, L ;
Xiao, W .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2003, 532 (1-2) :137-155
[3]   The two-step model for translesion synthesis: then and now [J].
Bridges, B .
MUTATION RESEARCH-DNA REPAIR, 2001, 485 (01) :61-67
[4]  
Dolinski KJ, 1999, GENETICS, V151, P935
[5]  
FALCO SC, 1983, GENETICS, V105, P857
[6]  
Fedorova IV, 1998, GENETICS, V148, P963
[7]  
Fedorova IV, 2000, GENETICS, V154, P495
[8]   The Saccharomyces cerevisiae MLH3 gene functions in MSH3-dependent suppression of frameshift mutations [J].
Flores-Rozas, H ;
Kolodner, RD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (21) :12404-12409
[9]  
FRIEDBERG EC, 1995, DNA REPAIR MUTAGENES
[10]   MECHANISMS OF DNA-MISMATCH CORRECTION [J].
GRILLEY, M ;
HOLMES, J ;
YASHAR, B ;
MODRICH, P .
MUTATION RESEARCH, 1990, 236 (2-3) :253-267