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转移性质粒RK2复制与转移相关基因间转换机制的剖析:trfAp对trbAp的优势及KorA调控转换的特异性基础

Dissection of the switch between genes for replication and transfer of promiscuous plasmid RK2: basis of the dominance of trfAp over trbAp and specificity for KorA in controlling the switch.

作者信息

Jagura-Burdzy G, Thomas C M

机构信息

School of Biological Sciences, University of Birmingham, Edgbaston, UK.

出版信息

J Mol Biol. 1997 Feb 7;265(5):507-18. doi: 10.1006/jmbi.1996.0747.

Abstract

The trfA and trb operons of broad host range plasmid RK2 are required for replication and conjugative transfer, respectively. Transcription of the trb operon can be initiated at one of two promoters: trbAp or trbBp. trbBp provides a burst of trb transcription on first entry into the cell. trbAp appears to be responsible for steady-state transcription of the trb operon as well as trbA, encoding a repressor which helps to shut down trbBp. The promoters trfAp and trbAp are arranged as face-to-face divergent promoters. trfAp is very strong and shuts off trbAp activity until trfAp is inhibited by KorA, one of the plasmid-encoded global regulators. Although trfAp is also repressed by KorB, a second global regulator encoded along with KorA in the central control operon, trbAp activation only occurs when KorA is present. KorB did not activate trbAp and indeed had a significant inhibitory effect on KorA activation. In vitro trfAp binds RNA polymerease (RNAP) approximately ten times more strongly than trbAp. Comparison of single and multiple rounds of in vitro run-off transcription suggested that the inhibitory effect of trfAp is due to elongating transcription complexes. In vitro studies with purified KorA and KorB on RNAP binding, isomerization and in vitro transcription suggested that both proteins can displace RNAP from trfAp, but that once open complexes have formed at either promoter they have a good chance of generating a transcript even if they encounter an opposing RNAP. In vivo KorB repressed trbAp even when trbAp was derepressed by a trfAp-1 mutation, removing the need for KorA. This suggested that KorB not only fails to derepress but actually represses trbAp despite the KorB operator being located 90 bp downstream of the transcription start point (tsp). By contrast KorA still activated trbAp when the two promoters were moved further apart or were brought so close that RNAP binding to the two promoters was mutually exclusive. Thus, KorA plays the dominant role in achieving the balance of expression of genes for alternate modes of plasmid propagation but its action is modulated by KorB.

摘要

广宿主范围质粒RK2的trfA和trb操纵子分别是复制和接合转移所必需的。trb操纵子的转录可以在两个启动子之一启动:trbAp或trbBp。trbBp在首次进入细胞时会引发一阵trb转录。trbAp似乎负责trb操纵子以及trbA的稳态转录,trbA编码一种阻遏物,有助于关闭trbBp。启动子trfAp和trbAp以面对面的反向启动子形式排列。trfAp非常强,在trfAp被质粒编码的全局调节因子之一KorA抑制之前,会关闭trbAp的活性。尽管trfAp也受到KorB的抑制,KorB是与KorA一起在中央控制操纵子中编码的第二个全局调节因子,但trbAp的激活仅在存在KorA时发生。KorB没有激活trbAp,实际上对KorA的激活有显著的抑制作用。在体外,trfAp与RNA聚合酶(RNAP)的结合强度比trbAp强约十倍。单轮和多轮体外径流转录的比较表明,trfAp的抑制作用是由于延伸的转录复合物。用纯化的KorA和KorB对RNAP结合、异构化和体外转录进行的体外研究表明,这两种蛋白质都可以将RNAP从trfAp上置换下来,但一旦在任何一个启动子上形成开放复合物,即使它们遇到相反的RNAP,它们也有很大机会产生转录本。在体内,即使trbAp因trfAp - 1突变而解除抑制,不再需要KorA,KorB仍会抑制trbAp。这表明,尽管KorB操纵子位于转录起始点(tsp)下游90 bp处,但KorB不仅不能解除trbAp的抑制,实际上还会抑制trbAp。相比之下,当两个启动子相距更远或靠得很近以至于RNAP与两个启动子的结合相互排斥时,KorA仍然会激活trbAp。因此,KorA在实现质粒传播交替模式的基因表达平衡中起主导作用,但其作用受到KorB的调节。

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