Kelberg Ekaterina P, Kovaltsova Svetlana V, Alekseev Sergey Yu, Fedorova Irina V, Gracheva Ludmila M, Evstukhina Tatiana A, Korolev Vladimir G
Laboratory of Eukaryote Genetics, Division of Molecular and Radiation Biophysics, Petersburg Nuclear Physics Institute, RAS, 188350 Orlova Roscha, Gatchina, Leningrad District, Russia.
Mutat Res. 2005 Oct 15;578(1-2):64-78. doi: 10.1016/j.mrfmmm.2005.03.003.
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 him1 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 him1 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.
我们鉴定出了一个新的酿酒酵母基因HIM1,它定位于第四条染色体的右臂(开放阅读框YDR317w),该基因的突变会导致自发突变率增加,并提高由紫外线、亚硝酸、甲基磺酸乙酯和甲磺酸甲酯诱导的突变频率。同时,him1突变不会导致对这些DNA损伤剂致死作用的敏感性增加。我们检测了携带him1突变和其他修复基因突变的双突变体中的诱导诱变情况:apn1突变阻断碱基切除修复;rad2、rev3和rad54突变阻断三条主要的DNA修复途径;pms1突变阻断错配修复;hsm2和hsm3突变会导致诱变效应。上位性分析表明him1与pms1、apn1和rad2突变存在协同相互作用,与rev3、rad54、hsm2和hsm3存在上位性。为了阐明HIM1在自发诱变控制中的作用,我们检测了him1突变体中DNA错配碱基的修复情况,发现与野生型菌株相比没有改变。我们认为,我们的结果表明HIM1基因参与了在DNA损伤易错旁路过程中出现的突变中间体加工的控制。