Prost J F, Nègre D, Oudot C, Murakami K, Ishihama A, Cozzone A J, Cortay J C
Institut de Biologie et Chimie des Protéines, Centre National de la Recherche Scientifique, Lyon, France.
J Bacteriol. 1999 Feb;181(3):893-8. doi: 10.1128/JB.181.3.893-898.1999.
The icd gene of Escherichia coli, encoding isocitrate dehydrogenase, was shown to be expressed from two different promoters: the previously identified icd P1 and a newly detected second promoter, icd P2, whose expression is positively regulated by the catabolite repressor-activator protein Cra, formerly called FruR. In each case, we determined the mRNA start site by primer extension analysis of in vivo transcripts and examined the interaction of the icd control region with either RNA polymerase or Cra. We observed that (i) the Cra factor binds to and activates transcription from a site centered at position -76.5 within the icd P2 promoter region and (ii) three particular mutations in the C-terminal end of the alpha subunit of RNA polymerase (L262A, R265A, and N268A) considerably diminish transcription initiating from the icd P2 promoter, as shown by in vitro experiments performed in the presence of mutant RNA polymerases carrying Ala substitutions.
大肠杆菌中编码异柠檬酸脱氢酶的icd基因可从两个不同的启动子表达:先前鉴定出的icd P1和新检测到的第二个启动子icd P2,其表达受分解代谢物阻遏激活蛋白Cra(以前称为FruR)正向调控。在每种情况下,我们通过对体内转录本进行引物延伸分析来确定mRNA起始位点,并研究icd调控区域与RNA聚合酶或Cra的相互作用。我们观察到:(i)Cra因子结合并激活icd P2启动子区域内以-76.5位置为中心的位点的转录;(ii)如在携带丙氨酸替代的突变RNA聚合酶存在下进行的体外实验所示,RNA聚合酶α亚基C末端的三个特定突变(L262A、R265A和N268A)显著减少了从icd P2启动子起始的转录。