酿酒酵母耐亚硝基胍新基因SNG1

Martin Grey , Claus T. Pich , Eckard Haase , Martin Brendel
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引用次数: 6

摘要

我们对SNG1基因进行了分子表征,当SNG1基因在多拷贝质粒上过表达时,该基因对突变原n -甲基-n ' -硝基-n -亚硝基胍(MNNG)具有超抗性。这种对MNNG的超抗性不是由于谷胱甘肽库的耗尽,因为含有酵母转化子的多拷贝SNG1至少含有野生型水平的谷胱甘肽;在这些转化体中,DNA修复似乎不受影响,因为在属于酵母修复突变体的三个寄生组的DNA修复突变体中也可以看到sng1介导的多拷贝MNNG超抗性。这表明SNG1不受YAP1编码的转录激活子的控制,而YAP1编码的转录激活子控制着酵母中至少两个参与MNNG代谢的基因的表达,SNG1无突变体是存活的,但对MNNG仅表现出轻微的敏感性,这表明SNG1不编码参与该突变原主要解毒步骤的蛋白质。对介导hyr的乘客DNA的测序显示,SNG1编码一个547 aa的多肽,其中包含7个可能是膜结合的跨膜区域。与已建立的基因数据库进行比对,结果表明SNG1是一个新的酵母基因。
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SNG1 — a new gene involved in nitrosoguanidine resistance in Saccharomyces cerevisiae

We have molecularly characterized the SNG1 gene that confers hyper-resistance to the mutagen N-methyl-N′-nitro-N-nitrosoguanidine (MNNG) in Saccharomyces cerevisiae when overexpressed on a multi-copy plasmid. This hyper-resistance to MNNG is not due to depletion of glutathione pools since multi-copy SNG1 containing yeast transformants contain at least wild type levels of glutathione; DNA repair seems unaffected in these transformants as the multi-copy SNG1-mediated MNNG hyper-resistance is also seen in DNA repair mutants belonging to each of the three epistasis groups of yeast repair mutants. It could be shown that SNG1 is not under control of the YAP1 encoded transcription activator that controls expression of at least two genes involved in MNNG metabolism in yeast, sng1 null mutants are viable but exhibit only slight sensitivity to MNNG, indicating that SNG1 does not encode a protein involved in a major detoxification step of this mutagen. Sequencing of the HYR-mediating passenger DNA revealed that SNG1 encodes a 547 aa polypeptide containing seven transmembrane-spanning regions that may be membrane-bound. Comparison of the DNA sequence with established gene databanks revealed that SNG1 is a novel yeast gene.

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