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丝状真菌构巢曲霉中的可诱导烷基转移酶DNA修复蛋白。

Inducible alkyltransferase DNA repair proteins in the filamentous fungus Aspergillus nidulans.

作者信息

Baker S M, Margison G P, Strike P

机构信息

Department of Genetics and Microbiology, University of Liverpool, UK.

出版信息

Nucleic Acids Res. 1992 Feb 25;20(4):645-51. doi: 10.1093/nar/20.4.645.

Abstract

We have investigated the response of the filamentous fungus Aspergillus nidulans to low, non-killing, doses of the alkylating agent MNNG (N-methyl-N'-nitro-N-nitrosoguanidine). Such treatment causes a substantial induction of DNA alkyltransferase activity, with the specific activity in treated cells increasing up to one hundred-fold. Fluorography reveals the two main inducible species as proteins of 18.5 kDa and 21 kDa, both of which have activity primarily against O6-methylguanine (O6-MeG) lesions. In addition, two other alkyltransferase proteins can also be detected. One, of MW 16 kDa, is expressed in non-treated cells, but is not induced to the same extent as the 18.5 and 21 kDa proteins. The other, a protein of 19.5 kDa, is highly inducible and can only be detected in treated cells. Unlike the other three proteins, it acts primarily against methyl-phosphotriester (Me-PT) lesions. This is the first instance in which an MePT alkyltransferase has been detected in a eukaryotic organism and, coupled with the high level of induction of the O6-MeG alkyltransferase enzymes, this indicates that a control system similar to the bacterial adaptive response may be present in filamentous fungi.

摘要

我们研究了丝状真菌构巢曲霉对低剂量、非致死剂量的烷基化剂MNNG(N-甲基-N'-硝基-N-亚硝基胍)的反应。这种处理会大量诱导DNA烷基转移酶活性,处理后细胞中的比活性增加高达100倍。荧光自显影显示,两种主要的可诱导蛋白分别为18.5 kDa和21 kDa,它们的活性主要针对O6-甲基鸟嘌呤(O6-MeG)损伤。此外,还能检测到另外两种烷基转移酶蛋白。一种分子量为16 kDa的蛋白在未处理的细胞中表达,但诱导程度不如18.5 kDa和21 kDa的蛋白。另一种19.5 kDa的蛋白高度可诱导,只能在处理后的细胞中检测到。与其他三种蛋白不同,它主要作用于甲基磷酸三酯(Me-PT)损伤。这是首次在真核生物中检测到MePT烷基转移酶,并且与O6-MeG烷基转移酶的高诱导水平相结合,这表明丝状真菌中可能存在类似于细菌适应性反应的控制系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82c9/311999/3b3af253c80f/nar00078-0015-a.jpg

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