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首页> 外文期刊>Biochimica et Biophysica Acta. Gene Regulatory Mechanisms >Elucidating the response of Kluyveromyces lactis to arsenite and peroxide stress and the role of the transcription factor KlYap8
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Elucidating the response of Kluyveromyces lactis to arsenite and peroxide stress and the role of the transcription factor KlYap8

机译:阐明乳酸克鲁维酵母对亚砷酸盐和过氧化物胁迫的反应以及转录因子KlYap8的作用

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All organisms need to sense and respond to a range of stress conditions. In this study, we used transcriptional profiling to identify genes and cellular processes that are responsive during arsenite and tert-butyl hydroperoxide exposure in Kluyveromyces lactis. Many arsenite-responsive genes encode proteins involved in redox processes, protein folding and stabilization, and transmembrane transport. The majority of peroxide-responsive genes encode functions related to transcription, translation, redox processes, metabolism and transport. A substantial number of these stress-regulated genes contain binding motifs for the AP-1 like transcription factors KlYap1 and KlYap8. We demonstrate that KlYap8 binds to and regulates gene expression through a 13 base-pair promoter motif, and that KlYap8 provides protection against arsenite, antimonite, cadmium and peroxide toxicity. Direct transport assays show that Klyap8δ cells accumulate more arsenic and cadmium than wild type cells and that the Klyap8δ mutant is defective in arsenic and cadmium export. KlYap8 regulates gene expression in response to both arsenite and peroxide, and might cooperate with KlYap1 in regulation of specific gene targets. Comparison of KlYap8 with its Saccharomyces cerevisiae orthologue ScYap8 indicates that KlYap8 senses and responds to multiple stress signals whereas ScYap8 is only involved in the response to arsenite and antimonite. Thus, our data suggest that functional specialization of ScYap8 has occurred after the whole genome duplication event. This is the first genome-wide stress response analysis in K. lactis and the first demonstration of KlYap8 function.
机译:所有生物都需要感知并应对一系列压力条件。在这项研究中,我们使用转录谱分析来鉴定在乳酸克鲁维酵母中砷和叔丁基过氧化氢暴露过程中有响应的基因和细胞过程。许多砷反应基因编码参与氧化还原过程,蛋白质折叠和稳定化以及跨膜转运的蛋白质。大多数过氧化物反应性基因编码与转录,翻译,氧化还原过程,代谢和运输有关的功能。这些应激调节基因中的大量含有AP-1的结合基序,如转录因子KlYap1和KlYap8。我们证明,KlYap8结合并通过一个13个碱基对的启动子基序调节基因表达,并且KlYap8提供了针对亚砷酸盐,锑矿,镉和过氧化物毒性的保护作用。直接转运试验表明,Klyap8δ细胞比野生型细胞积累更多的砷和镉,并且Klyap8δ突变体在砷和镉的出口方面存在缺陷。 KlYap8调节亚砷酸盐和过氧化物的基因表达,并可能与KlYap1协同调节特定的基因靶标。 KlYap8与其酿酒酵母直向同源物ScYap8的比较表明,KlYap8可感知并响应多种应激信号,而ScYap8仅参与对亚砷酸盐和锑矿的响应。因此,我们的数据表明,ScYap8的功能专业化已发生在整个基因组复制事件之后。这是乳酸克鲁维酵母中第一个全基因组范围的应激反应分析,也是KlYap8功能的第一个证明。

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