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多个启动子负责大肠杆菌K-12的glpEGR操纵子的转录。

Multiple promoters are responsible for transcription of the glpEGR operon of Escherichia coli K-12.

作者信息

Yang B, Larson T J

机构信息

Department of Biochemistry, Virginia Polytechnic Institute and State University, Blacksburg 24061-0308, USA.

出版信息

Biochim Biophys Acta. 1998 Mar 4;1396(1):114-26. doi: 10.1016/s0167-4781(97)00179-6.

Abstract

The transcriptional organization of the glpEGR genes of Escherichia coli was studied. Besides a promoter located upstream of the glpE start codon, three internal glpGR promoters were identified that express glpG and/or glpR (glp repressor). One promoter was located just upstream of the glpG start codon and two others (separated by several hundred base pairs) were located within glpG upstream of the glpR start codon. The transcriptional start points of these promoters were identified by primer extension analysis. The strengths of the individual promoters were compared by analysis of their expression when fused to a pormoter-probe vector. Analysis of the transcriptional expression of the glpEGR sequence with different combinations of the glpEGR promoters revealed no internal transcriptional terminators within the entire operon. Thus, the glpEGR genes are co-transcribed and form a single complex operon. The presence of multiple promoters may provide for differential expression of glpE, glpG and glpR. Potential regulation of the operon promoters by GlpR, catabolite repression, anaerobiosis or by FIS was studied. The glpE promoter was apparently controlled by the cAMP-CRP complex, but none of the promoters was responsive to specific repression by GlpR, to anaerobiosis or to FIS. Specific repression exerted by GlpR was characterized in vivo using glpD-lacZ and glpK-lacZ fusions. The degree of repression was correlated with the level of GlpR expression, and was inefficient when the glpD-encoded glycerol-P dehydrogenase was absent, presumably due to accumulation of the inducer, glycerol-P. This is in contrast to the previous conclusion that gpsA-encoded glycerol-P synthase tightly controls the cellular level of glycerol-P by end product inhibition.

摘要

对大肠杆菌glpEGR基因的转录组织进行了研究。除了位于glpE起始密码子上游的一个启动子外,还鉴定出三个内部glpGR启动子,它们表达glpG和/或glpR(glp阻遏物)。一个启动子位于glpG起始密码子的上游,另外两个(相隔几百个碱基对)位于glpR起始密码子上游的glpG内。通过引物延伸分析确定了这些启动子的转录起始点。通过分析与启动子探针载体融合时的表达情况,比较了各个启动子的强度。对具有不同glpEGR启动子组合的glpEGR序列的转录表达分析表明,整个操纵子内没有内部转录终止子。因此,glpEGR基因是共转录的,形成一个单一的复合操纵子。多个启动子的存在可能导致glpE、glpG和glpR的差异表达。研究了GlpR、分解代谢物阻遏、厌氧或FIS对操纵子启动子的潜在调控。glpE启动子显然受cAMP-CRP复合物的控制,但没有一个启动子对GlpR的特异性阻遏、厌氧或FIS有反应。使用glpD-lacZ和glpK-lacZ融合体在体内表征了GlpR施加的特异性阻遏。阻遏程度与GlpR表达水平相关,当缺乏glpD编码的甘油-P脱氢酶时,阻遏效率低下,这可能是由于诱导物甘油-P的积累所致。这与之前的结论相反,即gpsA编码的甘油-P合酶通过终产物抑制严格控制细胞内甘油-P的水平。

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