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转座子Tn501汞抗性基因的转录调控

Transcriptional regulation of the mercury-resistance genes of transposon Tn501.

作者信息

Lund P A, Ford S J, Brown N L

出版信息

J Gen Microbiol. 1986 Feb;132(2):465-80. doi: 10.1099/00221287-132-2-465.

Abstract

Expression of the mercury-resistance (mer) genes of the transposon Tn501 is positively and negatively controlled by the product of the merR gene. DNA sequence analysis has identified three open reading frames as potential candidates for this gene, one of which is oriented divergently with respect to the mercury-resistance genes. We have demonstrated that although RNA polymerase will bind to fragments containing the potential control regions for all three reading frames, only the control region for this divergent reading frame shows detectable promoter activity in vivo. Transcription of this reading frame is required for repression and induction of mer transcription. We have also shown that the Tn501 merR gene product negatively regulates its own synthesis, and have identified the start point of the transcript for this reading frame and for the mercury-inducible transcript of the mercury-resistance genes.

摘要

转座子Tn501的汞抗性(mer)基因的表达受merR基因产物的正调控和负调控。DNA序列分析已确定三个开放阅读框为该基因的潜在候选序列,其中一个与汞抗性基因的方向相反。我们已经证明,尽管RNA聚合酶会结合包含所有三个阅读框潜在控制区域的片段,但只有这个反向阅读框的控制区域在体内显示出可检测到的启动子活性。该阅读框的转录对于mer转录的抑制和诱导是必需的。我们还表明,Tn501 merR基因产物对其自身的合成起负调控作用,并确定了该阅读框以及汞抗性基因的汞诱导转录本的转录起点。

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