Motallebi-Veshareh M, Rouch D A, Thomas C M
School of Biological Sciences, University of Birmingham, UK.
Mol Microbiol. 1990 Sep;4(9):1455-63. doi: 10.1111/j.1365-2958.1990.tb02056.x.
Low copy-number bacterial plasmids F (the classical Escherichia coli sex factor) and prophage P1 encode partitioning functions which may provide fundamental insights into the active processes which ensure that bacterial genomes are segregated to both daughter cells prior to cell division. These partitioning systems involve two proteins: ParA and ParB. We report that incC from the broad host-range plasmid RK2 is a member of the family of ParA partitioning proteins and that these proteins (as well as related proteins encoded by plasmids from Agrobacterium tumefaciens and Chlamydia trachomatis) contain type I nucleotide-binding motifs. Also, we show that the cell division inhibitor MinD is homologous to members of the ParA family. Sequence comparisons of ParB proteins suggest that they may contain sites for phosphorylation. We propose that ATP hydrolysis by the ParA protein may result in phosphorylation of the ParB protein, thereby causing a conformational shift necessary to separate paired plasmid molecules at the cell division plane.
低拷贝数细菌质粒F(经典的大肠杆菌性因子)和原噬菌体P1编码分区功能,这可能为确保细菌基因组在细胞分裂前被分离到两个子细胞的活跃过程提供基本见解。这些分区系统涉及两种蛋白质:ParA和ParB。我们报告说,来自广宿主范围质粒RK2的incC是ParA分区蛋白家族的成员,并且这些蛋白质(以及根癌土壤杆菌和沙眼衣原体质粒编码的相关蛋白质)含有I型核苷酸结合基序。此外,我们表明细胞分裂抑制剂MinD与ParA家族的成员同源。ParB蛋白的序列比较表明它们可能含有磷酸化位点。我们提出,ParA蛋白的ATP水解可能导致ParB蛋白的磷酸化,从而引起在细胞分裂平面上分离配对质粒分子所需的构象转变。