Shadel G S, Baldwin T O
Center for Macromolecular Design, Institute of Biosciences and Technology, Texas A&M University, College Station 77843.
J Biol Chem. 1992 Apr 15;267(11):7696-702.
The LuxR protein is a transcriptional activator involved in regulation of the genes required for bioluminescence (lux) in the marine bacterium Vibrio fischeri. Transcription of the two divergently oriented lux operons (luxR and luxICDABEG) is activated by LuxR in the presence of a diffusible inducer (autoinducer). Transcription of the luxR gene is subject to both positive and negative autoregulation as well as activation by the cAMP-catabolite gene activator protein complex (cAMP-CAP). Transcription of luxR was studied using both luminescence in vivo as a reporter and primer extension analysis of mRNA synthesized in vivo. Mutation of the lux CAP-binding site resulted in a reduction in luminescence from the reporter and the complete loss of luxR positive autoregulation. Positive autoregulation was restored if luxR was provided in trans, demonstrating that LuxR and autoinducer activate luxR transcription in the absence of cAMP-CAP. By means of primer extension analysis, three sites of initiation of luxR transcription were demonstrated; initiation at two of these sites required cAMP-CAP. The quantity of all three transcripts was increased in the presence of LuxR and autoinducer when a plasmid with a wild-type CAP-binding site was used. Initiation at the cAMP-CAP-dependent sites was not observed from a plasmid with a mutated CAP-binding site in the presence or absence of autoinducer even with luxR supplied in trans. Instead, with luxR supplied in trans, initiation at the cAMP-CAP-independent initiation site was specifically stimulated by LuxR and autoinducer. Thus, in the course of positive autoregulation, the LuxR protein activates transcription from two luxR promoters by a cAMP-CAP-dependent mechanism and a third promoter by a cAMP-CAP-independent mechanism.
LuxR蛋白是一种转录激活因子,参与调控海洋细菌费氏弧菌中生物发光(lux)所需基因。在可扩散诱导物(自诱导物)存在的情况下,LuxR可激活两个方向相反的lux操纵子(luxR和luxICDABEG)的转录。luxR基因的转录既受到正反馈和负反馈调节,也受到cAMP-分解代谢物基因激活蛋白复合物(cAMP-CAP)的激活。利用体内发光作为报告基因以及对体内合成的mRNA进行引物延伸分析,对luxR的转录进行了研究。lux CAP结合位点的突变导致报告基因的发光减弱以及luxR正反馈调节完全丧失。如果通过反式提供luxR,则可恢复正反馈调节,这表明在没有cAMP-CAP的情况下,LuxR和自诱导物可激活luxR转录。通过引物延伸分析,证实了luxR转录的三个起始位点;其中两个位点的起始需要cAMP-CAP。当使用具有野生型CAP结合位点的质粒时,在LuxR和自诱导物存在的情况下,所有三种转录本的数量均增加。在存在或不存在自诱导物的情况下,即使通过反式提供luxR,从具有突变CAP结合位点的质粒中也未观察到在cAMP-CAP依赖性位点的起始。相反,在通过反式提供luxR的情况下,LuxR和自诱导物可特异性刺激在cAMP-CAP非依赖性起始位点的起始。因此,在正反馈调节过程中,LuxR蛋白通过cAMP-CAP依赖性机制激活来自两个luxR启动子的转录,并通过cAMP-CAP非依赖性机制激活第三个启动子的转录。