编码DNA聚合酶ζ催化亚基的(SCE)REV3果蝇同源物的分离和遗传特征

J.C.J. Eeken , R.J. Romeijn , A.W.M. de Jong , A. Pastink , P.H.M. Lohman
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引用次数: 24

摘要

在果蝇中,已知约有30个突变体对甲基化剂甲基甲烷磺酸盐(MMS)表现出超敏反应。将该药剂添加到培养基中导致突变体的幼虫死亡率增加。利用P插入诱变筛选,分离出三个对MMS敏感的II号染色体突变体。其中之一是已知EMS诱导的mus205(诱变剂敏感)突变体的等位基因。在新分离的突变体中,通过原位杂交在区域43E中检测到P元素。mus205在该地区的定位已通过缺陷测绘得到证实。该基因被克隆并显示出与酿酒酵母REV3基因的强同源性。REV3基因编码DNA聚合酶ζ的催化亚基,参与跨病变合成。P元件插入mus205基因的第一个外显子中,导致异常mRNA,编码一种假定的截短蛋白,该蛋白仅包含2130个氨基酸的果蝇天然蛋白的前13个。mus205突变体对烷基化剂和紫外线过敏,但对电离辐射不敏感。与报道的数据相反,在生殖细胞中,突变体对X射线、NQO和烷基化剂的突变性没有影响。在体细胞中,突变体对MMS诱导的突变和重组没有影响。果蝇mus205突变体的这种表型与酵母rev3突变体的表型显著不同,后者在紫外线、X射线、NQO和烷基化剂作用下是低突变的。
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Isolation and genetic characterisation of the Drosophila homologue of (SCE)REV3, encoding the catalytic subunit of DNA polymerase ζ

In Drosophila, about 30 mutants are known that show hypersensitivity to the methylating agent methyl methane sulfonate (MMS). Addition of this agent to the medium results in an increased larval mortality of the mutants. Using a P-insertion mutagenesis screen, three MMS-sensitive mutants on chromosome II were isolated. One of these is allelic to the known EMS-induced mus205 (mutagen sensitive) mutant. In the newly isolated mutant, a P-element is detected in region 43E by in situ hybridisation. The localisation of mus205 to this region was confirmed by deficiency mapping. The gene was cloned and shows strong homology to the Saccharomyces cerevisiae REV3 gene. The REV3 gene encodes the catalytic subunit of DNA polymerase ζ, involved in translesion synthesis. The P-element is inserted in the first exon of the mus205 gene resulting in an aberrant mRNA, encoding a putative truncated protein containing only the first 13 of the 2130 aa native Drosophila protein. The mus205 mutant is hypersensitive to alkylating agents and UV, but not to ionising radiation. In contrast to reported data, in germ cells, the mutant has no effect on mutability by X-rays, NQO and alkylating agents. In somatic cells, the mutant shows no effect on MMS-induced mutations and recombinations. This phenotype of the Drosophila mus205 mutant is strikingly different from the phenotype of the yeast rev3 mutant, which is hypomutable after UV, X-rays, NQO and alkylating agents.

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