Huang Meng-Er, Rio Anne-Gaelle, Nicolas Alain, Kolodner Richard D
Ludwig Institute for Cancer Research, Department of Medicine and Cancer Center, University of California at San Diego, School of Medicine, La Jolla, CA 92093, USA.
Proc Natl Acad Sci U S A. 2003 Sep 30;100(20):11529-34. doi: 10.1073/pnas.2035018100. Epub 2003 Sep 12.
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 (ii) 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 (EGL1) 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.
对4847个酵母基因缺失突变体文库进行了全基因组筛选,以鉴定在CAN1正向突变试验中抑制突变所需的基因。初步筛选及后续分析实现了:(i)鉴定出18个已知的突变体突变体,为检验筛选效率提供了可靠方法;(ii)鉴定出一些以前未知与抑制突变有关的基因。在以前未表征的突变抑制基因中,有6个功能未知的基因,其中4个(CSM2、SHU2、SHU1和YLR376c)编码相互作用并促进对甲磺酸甲酯杀伤抗性的蛋白质,1个基因(EGL1)以前被鉴定为抑制Ty1移动性和重复序列间的重组,还有1个基因(YLR154c)与任何已知过程均无关联。此外,发现5个与氧化应激反应有关的基因(TSA1、SOD1、LYS7、SKN7和YAP1)在突变抑制中起重要作用。而且,编码硫氧还蛋白过氧化物酶的TSA1被发现能强烈抑制染色体大片段重排。这些结果提供了参与预防诱变的非必需基因的全局视图。对这些基因的研究应能为鉴定可能与癌症易感性相关的人类基因及其作用机制提供有用线索。