Cui Z, Hirata D, Miyakawa T
Department of Molecular Biotechnology, Faculty of Engineering, Hiroshima University, Japan.
Biosci Biotechnol Biochem. 1999 Jan;63(1):162-7. doi: 10.1271/bbb.63.162.
The yeast gene SNQ2, which encodes a multidrug resistance ABC superfamily protein, is required for resistance to the mutagen 4-nitroquinoline N-oxide (4-NQO). The expression of the SNQ2 gene is under the control of a regulatory network that involves the transcription factor Yrr1p, as well as Pdr1p/Pdr3p (Cui et al., Mol. Microbiol., 29, 1307-1315 (1998)). By 5'-deletion analysis of the promoter by using SNQ2-lacZ fusion constructs, four regions: -745 to -639 (region I), -639 to -578 (region II), -548 to -533 (region III) and -533 to -485 (region IV) were found to be important for SNQ2 expression. Genetic analysis suggested that the site in region IV was responsible for the Yrr1p-mediated SNQ2 expression. A consensus motif known for the binding of Pdr1p/Pdr3p (PDRE) was not found in region IV.
酵母基因SNQ2编码一种多药耐药ABC超家族蛋白,它是对诱变剂4-硝基喹啉N-氧化物(4-NQO)产生抗性所必需的。SNQ2基因的表达受一个调控网络的控制,该网络涉及转录因子Yrr1p以及Pdr1p/Pdr3p(Cui等人,《分子微生物学》,29,1307 - 1315(1998))。通过使用SNQ2 - lacZ融合构建体对启动子进行5' - 缺失分析,发现四个区域:-745至-639(区域I)、-639至-578(区域II)、-548至-533(区域III)和-533至-485(区域IV)对SNQ2表达很重要。遗传分析表明区域IV中的位点负责Yrr1p介导的SNQ2表达。在区域IV中未发现已知的Pdr1p/Pdr3p结合共有基序(PDRE)。