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锌簇蛋白Rdr1p是编码多药转运蛋白的PDR5基因的转录抑制因子。

Zinc cluster protein Rdr1p is a transcriptional repressor of the PDR5 gene encoding a multidrug transporter.

作者信息

Hellauer Karen, Akache Bassel, MacPherson Sarah, Sirard Edith, Turcotte Bernard

机构信息

Department of Medicine, McGill University Health Centre, Royal Victoria Hospital, McGill University, Montréal, Québec H3A 1A1, Canada.

出版信息

J Biol Chem. 2002 May 17;277(20):17671-6. doi: 10.1074/jbc.M201637200. Epub 2002 Mar 6.

Abstract

The yeast PDR5 gene encodes an efflux pump that confers multidrug resistance. Expression of PDR5 is positively regulated by the transcription factors Pdr1p and Pdr3p that recognize the same pleiotropic drug resistance elements (PDREs) in the PDR5 promoter. Pdr1p and Pdr3p belong to the Gal4p family of zinc cluster proteins. The function of RDR1 (YOR380W), which also encodes a member of this family, is unknown. To identify target genes for Rdr1p, we have performed whole-genome analysis of gene expression with DNA microarrays. Our results show that Rdr1p is a transcriptional repressor of five genes, including PDR5. A Deltardr1 strain has increased resistance to cycloheximide, as expected from the overexpression of PDR5. In addition, the activity of a PDR5-lacZ reporter is increased in a Deltardr1 strain. All (but one) genes affected by removal of Rdr1p contain PDREs in their promoters. We tested if the effect of Rdr1p is mediated through PDREs by inserting this DNA element in front of a minimal promoter. Activity of this reporter was increased in a Deltardr1 strain. Moreover, mutations known to reduce binding of Pdr1/Pdr3p abolished the induction observed in the Deltardr1 strain. Thus, we have identified a transcriptional repressor involved in the control of multidrug resistance.

摘要

酵母PDR5基因编码一种赋予多药耐药性的外排泵。PDR5的表达受转录因子Pdr1p和Pdr3p的正向调控,这两种转录因子可识别PDR5启动子中相同的多效性耐药元件(PDREs)。Pdr1p和Pdr3p属于锌簇蛋白的Gal4p家族。同样编码该家族成员之一的RDR1(YOR380W)的功能尚不清楚。为了确定Rdr1p的靶基因,我们利用DNA微阵列对基因表达进行了全基因组分析。我们的结果表明,Rdr1p是包括PDR5在内的五个基因的转录抑制因子。正如PDR5过表达所预期的那样,缺失Rdr1的菌株对环己酰亚胺的抗性增强。此外,PDR5 - lacZ报告基因在缺失Rdr1的菌株中的活性增加。所有(除一个外)受Rdr1缺失影响的基因在其启动子中都含有PDREs。我们通过在最小启动子前插入该DNA元件来测试Rdr1p的作用是否通过PDREs介导。该报告基因的活性在缺失Rdr1的菌株中增加。此外,已知可减少Pdr1/Pdr3p结合的突变消除了在缺失Rdr1的菌株中观察到的诱导作用。因此,我们鉴定出了一种参与多药耐药性控制的转录抑制因子。

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