Cui Z, Shiraki T, Hirata D, Miyakawa T
Department of Molecular Biotechnology, Faculty of Engineering, Hiroshima University, Higashi-Hiroshima, Japan.
Mol Microbiol. 1998 Sep;29(5):1307-15. doi: 10.1046/j.1365-2958.1998.01027.x.
We have cloned and characterized a Saccharomyces cerevisiae gene YRR1 that is important for resistance to the mutagen 4-nitroquinoline N-oxide (4-NQO). The wild-type YRR1 gene encodes a protein that contains a Zn(II)2Cys6-type zinc-finger motif. Disruption of the YRR1 gene leads to hypersensitivity to 4-NQO. A dominant mutation (YRR1-1) that confers strong resistance to 4-NQO has been identified. Epistasis analysis demonstrated that 4-NQO resistances mediated by the YRR1 and YRR1-1 alleles require the presence of the SNQ2 gene that encodes a multidrug resistance ATP binding cassette superfamily protein responsible for 4-NQO export. Northern blot analysis of SNQ2 mRNA levels indicated that Yrr1p is involved in basal and drug-induced transcriptional activation of SNQ2, whereas Pdr1p/Pdr3p transcription factors are mainly involved in basal SNQ2 expression. In the YRR1-1 mutant, the level of SNQ2 mRNA is constitutively elevated. These results establish that Yrr1p is important for 4-NQO resistance by mediating transcriptional activation of the SNQ2 gene in response to the stress imposed by 4-NQO. The gain-of-function mutation of Yrr1-1p was attributable to the duplication of a 12-amino-acid sequence generated near the carboxy terminus.
我们已经克隆并鉴定了酿酒酵母基因YRR1,该基因对于抵抗诱变剂4-硝基喹啉N-氧化物(4-NQO)很重要。野生型YRR1基因编码一种包含Zn(II)2Cys6型锌指基序的蛋白质。YRR1基因的破坏导致对4-NQO超敏。已鉴定出一种对4-NQO具有强抗性的显性突变(YRR1-1)。上位性分析表明,由YRR1和YRR1-1等位基因介导的4-NQO抗性需要存在SNQ2基因,该基因编码一种负责4-NQO输出的多药抗性ATP结合盒超家族蛋白。对SNQ2 mRNA水平的Northern印迹分析表明,Yrr1p参与SNQ2的基础转录和药物诱导的转录激活,而Pdr1p/Pdr3p转录因子主要参与SNQ2的基础表达。在YRR1-1突变体中,SNQ2 mRNA水平组成性升高。这些结果表明,Yrr1p通过介导SNQ2基因的转录激活以响应4-NQO施加的应激,对4-NQO抗性很重要。Yrr1-1p的功能获得性突变归因于在羧基末端附近产生的一个12个氨基酸序列的重复。