Kulmburg P, Mathieu M, Dowzer C, Kelly J, Felenbok B
Institut de Génétique et Microbiologie, UPS, Orsay, France.
Mol Microbiol. 1993 Mar;7(6):847-57. doi: 10.1111/j.1365-2958.1993.tb01175.x.
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.
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。