首页> 美国卫生研究院文献>Nucleic Acids Research >Gene regulation on broad host range plasmid RK2: identification of three novel operons whose transcription is repressed by both KorA and KorC.
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Gene regulation on broad host range plasmid RK2: identification of three novel operons whose transcription is repressed by both KorA and KorC.

机译:广泛的宿主范围质粒RK2的基因调控:鉴定三个新操纵子它们的转录均被KorA和KorC抑制。

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摘要

The product of the korA gene of broad host range plasmid RK2 is a key transcriptional repressor which regulates not only the expression of the essential replication gene trfA but also its own expression and that of the kilA operon. It has previously been proposed that korA also encodes a positive activator of transcription of the korC gene, which may act as a transcriptional antiterminator. Here we show that the action of korA in relation to korC can be explained entirely through the korA protein's property as a transcriptional repressor. The limited ability of the previously cloned korC gene to suppress kilC on its own is shown to be due to the fact that korC in RK2 is transcribed from the bla promoter of Tn1 which was deleted in the original korC clones. We demonstrate that korA is a second repressor along with korC of three operons, one of which encodes kilC, the other two not having been described previously and serving an as yet unknown function. We have designated these operons kcrA, B and C for KorC-regulated. Putative kilC is designated kcrC. The homology between the expression signals of these operons suggests that they have arisen by duplication. This is confirmed in the case of kcrA and B by the existence of considerable homology between the products of the first ORFs in each of these operons.
机译:宿主范围广的质粒RK2的korA基因的产物是关键的转录阻遏物,其不仅调节必需的复制基因trfA的表达,而且调节其自身的表达和kilA操纵子的表达。先前已经提出,korA还编码korC基因的转录的正激活剂,其可以充当转录抗终止剂。在这里,我们显示korA相对于korC的作用可以完全通过korA蛋白作为转录阻遏物的特性来解释。先前克隆的korC基因单独抑制kilC的能力有限,这是由于RK2中的korC是从Tn1的bla启动子转录而来的,该启动子在原始korC克隆中被删除。我们证明,korA与三个操纵子的korC一起是第二个阻遏物,其中一个操纵子编码kilC,另外两个以前没有被描述过,并且起未知的作用。我们已将这些操纵子kcrA,B和C指定为KorC调控的。假定的kilC称为kcrC。这些操纵子的表达信号之间的同源性表明它们是通过复制产生的。在kcrA和B的情况下,通过在每个操纵子中的第一个ORF产物之间存在相当的同源性,可以证实这一点。

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