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构巢曲霉中紫外线诱变所需的uvsI基因编码一种与REV3同源的蛋白,REV3是酵母DNA聚合酶ζ的一个亚基,参与跨损伤DNA合成。

The uvsI gene of Aspergillus nidulans required for UV-mutagenesis encodes a homolog to REV3, a subunit of the DNA polymerase zeta of yeast involved in translesion DNA synthesis.

作者信息

Han K Y, Chae S K, Han D M

机构信息

Dept. of Molecular Biology, Wonkwang University, Iksan, South Korea.

出版信息

FEMS Microbiol Lett. 1998 Jul 1;164(1):13-9. doi: 10.1111/j.1574-6968.1998.tb13061.x.

Abstract

Defects in the uvsI gene of Aspergillus nidulans resulted in high UV sensitivity and reductions of spontaneous and UV-induced reversion of certain alleles, uvsl;uvsA double mutants exhibited high methyl methane sulfonate (MMS)-sensitivity in contrast to the slight sensitivity of the component single mutants. Using such a double mutant as recipient, a clone complementing uvsI501 has been isolated from a chromosome III specific library. The deduced amino acid sequence from the 1.1-kb sequenced region, a part of the 5.2-kb DNA fragment showing uvsI-complementing activity, had a 62% identity with REV3 of yeast. Disruptants of the cloned gene demonstrated the same level of sensitivity to UV light as uvsI and failed to complement uvsI501 in heterozygous diploids.

摘要

构巢曲霉uvsI基因的缺陷导致其对紫外线高度敏感,某些等位基因的自发回复突变率和紫外线诱导的回复突变率降低,uvsI;uvsA双突变体表现出对甲磺酸甲酯(MMS)高度敏感,而单个组成突变体仅有轻微敏感。以这样的双突变体作为受体,从III号染色体特异性文库中分离出了一个能互补uvsI501的克隆。从显示uvsI互补活性的5.2-kb DNA片段的一部分1.1-kb测序区域推导的氨基酸序列与酵母的REV3有62%的同一性。克隆基因的破坏体对紫外线的敏感程度与uvsI相同,并且在杂合二倍体中不能互补uvsI501。

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