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Kluyveromyces lactis 中转录激活型 KlPDR1 基因对多药耐药性的控制。

Autoactivated KlPDR1 gene in the control of multidrug resistance in Kluyveromyces lactis.

机构信息

Comenius University in Bratislava, Department of Microbiology and Virology, Slovak Republic.

出版信息

Can J Microbiol. 2011 Oct;57(10):844-9. doi: 10.1139/w11-071. Epub 2011 Sep 27.

Abstract

The KlPDR1 gene encodes a zinc finger transcription factor that has recently been shown to be involved in the control of multidrug resistance of Kluyveromyces lactis . In this work, we provide evidence that the K. lactis KlPDR1 gene is under positive autoregulation by KlPdr1p, which plays a role in the activation of the main multidrug resistance transporter gene KlPDR5. Electrophoretic mobility shift assays, as well as the use of gusA reporter constructs, enabled us to identify the 5'-tataTCCGGGTAactt-3' sequence motif in the KlPDR1 promoter (in the position -326 to -319 bp) as the PDRE (pleiotropic drug responsive element) for the binding of KlPdr1p. The drug sensitivity of Klpdr1Δ mutant cells was complemented by introducing the plasmid-born KlPDR1 gene. The KlPdr1p activated the expression of the P(KlPDR1)-gusA fusion gene, and the expression of the KlPDR1 gene was induced by fluconazole. The PDRE was also found in the promoter of KlPDR5, a gene encoding the ATP-dependent efflux pump responsible for the drug resistance phenomenon in K. lactis.

摘要

KlPDR1 基因编码一种锌指转录因子,最近研究表明其参与了乳酸克鲁维酵母多药耐药性的调控。在这项工作中,我们提供了证据表明,KlPdr1p 对 KlPDR1 基因进行正调控,KlPdr1p 在激活主要多药耐药转运蛋白基因 KlPDR5 的过程中发挥作用。电泳迁移率变动分析以及使用 gusA 报告基因构建体,使我们能够确定 KlPDR1 启动子中的 5'-tataTCCGGGTAactt-3' 序列基序(-326 至-319 bp 位置)为 KlPdr1p 结合的 PDRE(多药响应元件)。KlPDR1 基因的质粒表达可以弥补 Klpdr1Δ 突变细胞的药物敏感性。KlPdr1p 激活了 P(KlPDR1)-gusA 融合基因的表达,氟康唑诱导了 KlPDR1 基因的表达。在编码负责乳酸克鲁维酵母耐药现象的 ATP 依赖性外排泵的 KlPDR5 基因的启动子中也发现了 PDRE。

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