首页> 美国卫生研究院文献>Journal of Bacteriology >Regulation of the transfer genes of Streptomyces plasmid pSN22: in vivo and in vitro study of the interaction of TraR with promoter regions.
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Regulation of the transfer genes of Streptomyces plasmid pSN22: in vivo and in vitro study of the interaction of TraR with promoter regions.

机译:链霉菌质粒pSN22转移基因的调控:TraR与启动子区域相互作用的体内和体外研究。

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摘要

Expression of the tra operon, essential for conjugative transfer of the 11-kb Streptomyces nigrifaciens plasmid pSN22, is negatively regulated by traR, which is located upstream of the tra operon and transcribed in the opposite orientation. The transcriptional start points for the tra and traR mRNAs were determined by primer extension; they are 72 bp apart and have identical -10 promoter sequences. The TraR protein was overexpressed in Escherichia coli and used for gel retardation and DNase I protection experiments. It bound specifically to the bidirectional tra-traR promoter region and protected four DNA regions, each of which contains a similar 12-bp sequence. The binding was strongest to the region downstream of the tra promoter, probably ensuring that expression of the potentially lethal traB gene is turned off before traR. The efficiency of intramycelial plasmid transfer was decreased by the mutation at the downstream region.
机译:tra操纵子的表达对于11 kb黑链霉菌质粒pSN22的共轭转移至关重要,其表达受traR负调控,它位于tra操纵子的上游并以相反的方向转录。 tra和traR mRNA的转录起点通过引物延伸来确定;它们相距72 bp,具有相同的-10启动子序列。 TraR蛋白在大肠杆菌中过表达,并用于凝胶阻滞和DNase I保护实验。它与双向tra-traR启动子区域特异性结合,并保护了四个DNA区域,每个区域都包含相似的12 bp序列。与tra启动子下游区域的结合最强,这可能确保在traR之前关闭可能致命的traB基因的表达。下游区域中的突变降低了菌丝内质粒转移的效率。

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