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酿酒酵母的Rgt1转录因子如何受葡萄糖调控。

How the Rgt1 transcription factor of Saccharomyces cerevisiae is regulated by glucose.

作者信息

Polish Jeffrey A, Kim Jeong-Ho, Johnston Mark

机构信息

Department of Genetics, Washington University, Saint Louis, Missouri 63110, USA.

出版信息

Genetics. 2005 Feb;169(2):583-94. doi: 10.1534/genetics.104.034512. Epub 2004 Oct 16.

Abstract

Rgt1 is a transcription factor that regulates expression of HXT genes encoding glucose transporters in the yeast Saccharomyces cerevisiae. Rgt1 represses HXT gene expression in the absence of glucose; high levels of glucose cause Rgt1 to activate expression of HXT1. We identified four functional domains of Rgt1. A domain required for transcriptional repression (amino acids 210-250) is required for interaction of Rgt1 with the Ssn6 corepressor. Another region of Rgt1 (320-380) is required for normal transcriptional activation, and sequences flanking this region (310-320 and 400-410) regulate this function. A central region (520-830) and a short sequence adjacent to the zinc cluster DNA-binding domain (80-90) inhibit transcriptional repression when glucose is present. We found that this middle region of Rgt1 physically interacts with the N-terminal portion of the protein that includes the DNA-binding domain. This interaction is inhibited by the Rgt1 regulator Mth1, which binds to Rgt1. Our results suggest that Mth1 promotes transcriptional repression by Rgt1 by binding to it and preventing the intramolecular interaction, probably by preventing phosphorylation of Rgt1, thereby enabling Rgt1 to bind to DNA. Glucose induces HXT1 gene expression by causing Mth1 degradation, allowing Rgt1 phosphorylation, and leading to the intramolecular interaction that inhibits DNA binding of Rgt1.

摘要

Rgt1是一种转录因子,可调节酿酒酵母中编码葡萄糖转运蛋白的HXT基因的表达。在没有葡萄糖的情况下,Rgt1会抑制HXT基因的表达;高浓度葡萄糖会使Rgt1激活HXT1的表达。我们鉴定出了Rgt1的四个功能结构域。转录抑制所需的结构域(氨基酸210 - 250)是Rgt1与Ssn6共抑制因子相互作用所必需的。Rgt1的另一个区域(320 - 380)是正常转录激活所必需的,该区域两侧的序列(310 - 320和400 - 410)调节此功能。一个中央区域(520 - 830)和锌簇DNA结合结构域相邻的短序列(80 - 90)在有葡萄糖存在时会抑制转录抑制。我们发现Rgt1的这个中间区域与包含DNA结合结构域的蛋白质N端部分发生物理相互作用。这种相互作用受到与Rgt1结合的Rgt1调节因子Mth1的抑制。我们的结果表明,Mth1通过与Rgt1结合并阻止分子内相互作用来促进Rgt1的转录抑制,可能是通过阻止Rgt1的磷酸化,从而使Rgt1能够结合DNA。葡萄糖通过导致Mth1降解、允许Rgt1磷酸化并导致抑制Rgt1与DNA结合的分子内相互作用来诱导HXT1基因表达。

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