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RPD3 and ROM2 are required for multidrug resistance in Saccharomyces cerevisiae

机译:RPD3和ROM2是酿酒酵母中多重耐药性所必需的

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摘要

The PDR5 gene encodes the major multidrug resistance efflux pump in Saccharomyces cerevisiae. In drug-resistant cells, the hyperactive Pdr1p or Pdr3p transcriptional activators are responsible for the PDR5 upregulation. In this work, it is shown that the RPD3 gene encoding the histone deacetylase that functions as a transcriptional corepressor at many promoters and the ROM2 gene coding for the GDP/GTP exchange protein for Rho1p and Rho2p participating in signal transduction pathways are required for PDR5 transcription under cycloheximide-induced and noninduced conditions. Transposon insertion mutations in ROM2, RPD3 and some other genes encoding specific subunits of the large Rpd3L protein complex resulted in enhanced susceptibility of mutant cells to antifungals. In the rpd3 and rom2 mutants, the level of PDR5 mRNA and the rate of rhodamine 6G efflux were reduced. Unlike rpd3, in rom2 mutant cells the drug hypersensitivity and the defect in PDR5 expression were suppressed by PDR1 or PDR3 overexpressed from heterologous promoters and by the hyperactive pdr3-9 mutant allele. The results indicate that Rpd3p histone deacetylase participating in chromatin remodeling and Rom2p participating in the cell integrity pathway are involved in the control of PDR5 expression and modulation of multidrug resistance in yeast.
机译:PDR5基因编码啤酒酵母中主要的多药耐药性外排泵。在耐药细胞中,过度活跃的Pdr1p或Pdr3p转录激活因子负责PDR5的上调。在这项工作中,表明PDR5转录需要编码在许多启动子上起转录共抑制物作用的组蛋白脱乙酰基酶的RPD3基因和编码参与信号转导途径的Rho1p和Rho2p的GDP / GTP交换蛋白的ROM2基因。在环己酰亚胺诱导和非诱导条件下。 ROM2,RPD3和其他一些编码大Rpd3L蛋白复合物特定亚基的基因的转座子插入突变导致突变细胞对抗真菌药的敏感性增强。在rpd3和rom2突变体中,PDR5 mRNA的水平和若丹明6G外排的速率降低。与rpd3不同,在rom2突变细胞中,药物异敏性和PDR5表达缺陷被异源启动子过表达的PDR1或PDR3以及过度活跃的pdr3-9突变等位基因抑制。结果表明,参与染色质重塑的Rpd3p组蛋白脱乙酰基酶和参与细胞完整性途径的Rom2p参与了酵母中PDR5表达的控制和多药耐药性的调控。

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