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首页> 外文期刊>FEMS Microbiology Letters >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
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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

机译:UV诱变所需的构巢曲霉的uvsI基因编码与REV3的同源物,REV3是酵母的DNA聚合酶zeta的一个亚基,参与跨病害DNA合成

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摘要

Defects in the uvsI gene of Aspergillus nidulans resulted in high UV sensitivity and reductions of spontaneous and UV-induced reversion of certain alleles. uvsI, 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 Ill;sl-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. (C) 1998 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved. [References: 28]
机译:构巢曲霉uvsI基因的缺陷导致高紫外线敏感性,并减少了某些等位基因的自发和紫外线诱导的逆转。 uvsI,uvsA双重突变体表现出高的甲基甲烷磺酸甲酯(MMS)敏感性,与单个突变体的轻微敏感性相反。使用这样的双重突变体作为受体,已经从染色体III特异性文库分离了互补uvsI501的克隆。从1.1kb序列区推导的氨基酸序列,即5.2kb DNA片段的一部分,显示III,s1互补活性,与酵母的REV3具有62%的同一性。克隆的基因破坏者对紫外线的敏感性与uvsI相同,并且不能在杂合二倍体中补充uvsI501。 (C)1998年欧洲微生物学会联合会。由Elsevier Science B.V.保留所有权利。 [参考:28]

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