Repair of alkylation damage in the fungus Aspergillus nidulans

Richard A. Swirski, Susan G. Shawcross, Barry M. Faulkner, Peter Strike
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引用次数: 9

Abstract

The repair of alkylation damage in Aspergillus nidulans was investigated. We have assayed soluble protein fractions for enzymes known to be involved in the repair of this type of damage in DNA. The presence of a glycosylase activity that can remove 3-methyladenine from DNA was demonstrated, as well as a DNA methyltransferase activity that appears to act against O6-methylguanine.

In addition to this approach, a series of mutants were isolated which display increased sensitivity to alkylating agents (sag mutants). 5 such mutants were further characterized, and at least 4 are shown to map to genes which have not previously been characterized. The behaviour of double mutant combinations demonstrates the existence of at least 2 pathways for the repair of alkylation damage. The majority of the sag mutants (sagA1, sagB2, sag4 and sagE5) exhibit an increased sensitivity to a range of alkylating agents, but not to UV light, while sagC3, when irradiated at the germling stage, also shows sensitivity to UV. None of the mutants isolated are defective in either the 3-methyladenine DNA glycosylase activity, or the DNA methyltransferase activity, and the nature of the defects in these strains remains to be determined.

木质素曲霉烷基化损伤的修复
研究了空心曲霉烷基化损伤的修复。我们已经分析了可溶性蛋白的酶,已知这些酶参与了DNA中这类损伤的修复。糖基化酶活性的存在可以从DNA中去除3-甲基腺嘌呤,以及DNA甲基转移酶活性似乎对o6 -甲基鸟嘌呤起作用。除了这种方法之外,还分离出一系列对烷基化剂(sag突变体)敏感性增加的突变体。5个这样的突变体被进一步表征,至少有4个被证明与以前没有被表征的基因相对应。双突变体组合的行为表明至少存在两种修复烷基化损伤的途径。大多数突变体(sagA1、sagB2、sag4和sagE5)对一系列烷基化剂的敏感性增加,但对紫外光的敏感性没有增加,而sagC3在苗期辐照时也对紫外光敏感。分离的突变体在3-甲基腺嘌呤DNA糖基酶活性或DNA甲基转移酶活性方面都没有缺陷,这些菌株的缺陷性质仍有待确定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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