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构巢曲霉中乙醇调节子的alcR和alcA启动子上的特异性结合位点,用于CREA阻遏物介导碳分解代谢物阻遏。

Specific binding sites in the alcR and alcA promoters of the ethanol regulon for the CREA repressor mediating carbon catabolite repression in Aspergillus nidulans.

作者信息

Kulmburg P, Mathieu M, Dowzer C, Kelly J, Felenbok B

机构信息

Institut de Génétique et Microbiologie, UPS, Orsay, France.

出版信息

Mol Microbiol. 1993 Mar;7(6):847-57. doi: 10.1111/j.1365-2958.1993.tb01175.x.

Abstract

The CREA repressor responsible for carbon catabolite repression in Aspergillus nidulans represses the transcription of the ethanol regulon. The N-terminal part of the CREA protein encompassing the two zinc fingers (C2H2 class family) and an alanine-rich region was expressed in Escherichia coli as a fusion protein with glutathione-S-transferase. Our results show that CREA is a DNA-binding protein able to bind to the promoters of both the specific trans-acting gene, alcR, and of the structural gene, alcA, encoding the alcohol dehydrogenase I. DNase I protection footprinting experiments revealed several specific binding sites in the alcR and in the alcA promoters having the consensus sequence 5'-G/CPyGGGG-3'. The disruption of one of these CREA-binding sites in the alcR promoter overlapping the induction target for the trans-activator ALCR results in a partially derepressed alc phenotype and derepressed alcR transcription, showing that this binding site is functional in vivo. Our data suggest that CREA represses the ethanol regulon by a double lock mechanism repressing both the trans-acting gene, alcR, and the structural gene, alcA.

摘要

负责构巢曲霉中碳代谢物阻遏的CREA阻遏蛋白可抑制乙醇调节子的转录。CREA蛋白的N端部分包含两个锌指结构(C2H2类家族)和一个富含丙氨酸的区域,在大肠杆菌中作为与谷胱甘肽-S-转移酶的融合蛋白进行表达。我们的结果表明,CREA是一种DNA结合蛋白,能够与特定反式作用基因alcR以及编码乙醇脱氢酶I的结构基因alcA的启动子结合。DNase I保护足迹实验揭示了alcR和alcA启动子中的几个具有一致序列5'-G/CPyGGGG-3'的特异性结合位点。alcR启动子中与反式激活因子ALCR的诱导靶点重叠的一个CREA结合位点的破坏导致部分去阻遏的alc表型和去阻遏的alcR转录,表明该结合位点在体内具有功能。我们的数据表明,CREA通过双重锁定机制抑制乙醇调节子,同时抑制反式作用基因alcR和结构基因alcA。

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