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广宿主IncP质粒的全局调控因子KorB远距离抑制作用

Repression at a distance by the global regulator KorB of promiscuous IncP plasmids.

作者信息

Jagura-Burdzy G, Macartney D P, Zatyka M, Cunliffe L, Cooke D, Huggins C, Westblade L, Khanim F, Thomas C M

机构信息

School of Biological Sciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.

出版信息

Mol Microbiol. 1999 May;32(3):519-32. doi: 10.1046/j.1365-2958.1999.01365.x.

DOI:10.1046/j.1365-2958.1999.01365.x
PMID:10320575
Abstract

KorB protein (358 amino acids) binds to 12 highly conserved sequences on the RK2 genome and co-ordinates the expression of at least five operons encoding genes for stable inheritance and plasmid transfer. KorB represses the trfA, korA and klaA promoters where it binds 4 bp upstream of the -35 region (class I KorB operators, OB). We show here that KorB on its own can also repress the trbA, trbB, kfrA and kleA promoters where OB is between 80 and 189 bp away from the transcription start point (class II operator). A C-terminal deletion of 17 amino acids resulted in the loss of KorB's ability to repress through class II operator but not through class I operator. This deletion reduced multimerization of His6-tailed KorB protein in vitro and greatly reduced binding specificity for fragments containing OB sequences. At the trbBp region, where OB9 lies 189 bp upstream of the transcription start point, mutagenesis of a proposed secondary binding site overlapping the trbBp -35 region had no effect on the ability of KorB to repress trbBp. Nevertheless, gel retardation analysis showed that KorB binding is promoted by sequences upstream and downstream of OB9 and that KorB can form higher order complexes on DNA. However, DNase I footprinting suggested that RNA polymerase may interact directly with KorB bound at OB9 and implied that contacts between these proteins could be responsible for the action of KorB at a distance.

摘要

KorB蛋白(358个氨基酸)与RK2基因组上12个高度保守的序列结合,并协调至少五个操纵子的表达,这些操纵子编码用于稳定遗传和质粒转移的基因。KorB抑制trfA、korA和klaA启动子,它在-35区域上游4 bp处结合(I类KorB操纵子,OB)。我们在此表明,单独的KorB也可以抑制trbA、trbB、kfrA和kleA启动子,其中OB距离转录起始点80至189 bp(II类操纵子)。C末端缺失17个氨基酸导致KorB通过II类操纵子抑制的能力丧失,但通过I类操纵子抑制的能力未丧失。这种缺失降低了His6尾KorB蛋白在体外的多聚化,并大大降低了对含有OB序列片段的结合特异性。在trbBp区域,OB9位于转录起始点上游189 bp处,对与trbBp -35区域重叠的假定二级结合位点进行诱变对KorB抑制trbBp的能力没有影响。然而,凝胶阻滞分析表明,OB9上下游的序列促进了KorB的结合,并且KorB可以在DNA上形成高阶复合物。然而,DNase I足迹分析表明,RNA聚合酶可能直接与结合在OB9处的KorB相互作用,并暗示这些蛋白质之间的接触可能是KorB远距离作用的原因。

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