Biochemistry Department, The University of Texas Health Science Center at Tyler, Tyler, TX 75708, USA.
Tuberculosis (Edinb). 2009 Dec;89 Suppl 1(Suppl 1):S65-9. doi: 10.1016/S1472-9792(09)70015-0.
The ParA and ParB family proteins are required for accurate partitioning of replicated chromosomes. The Mycobacterium tuberculosis genome contains parB, parA and two parA homologs, Rv1708 and Rv3213c. It is unknown if parA and its homologs are functionally related. To understand the roles of ParA and ParB proteins in M. tuberculosis cell cycle, we have evaluated the consequences of their overproduction and visualized their localization patterns in M. smegmatis. We show that cells overproducing ParA, Rv1708 and Rv3213c and ParB are filamentous and multinucleoidal indicating defects in cell-cycle progression. Visualization of green-fluorescent protein fusions of ParA and its homologues showed similar localization patterns with foci at poles, quarter-cell, midcell positions and spiral-like structures indicating that they are functionally related. On the other hand, the ParB- GFP fusion protein localized only to the cell poles. The cyan- and yellow-fluorescent fusion proteins of ParA and ParB, respectively, colocalized at the cell poles indicating that these proteins interact and possibly associate with the chromosomal origin of replication. Collectively our results suggest that the M. tuberculosis Par proteins play important roles in cell-cycle progression.
ParA 和 ParB 家族蛋白是染色体复制准确分配所必需的。结核分枝杆菌基因组包含 parB、parA 和两个 parA 同源物,Rv1708 和 Rv3213c。目前尚不清楚 parA 及其同源物是否具有功能相关性。为了了解 ParA 和 ParB 蛋白在结核分枝杆菌细胞周期中的作用,我们评估了它们过表达的后果,并在耻垢分枝杆菌中可视化了它们的定位模式。我们表明,过表达 ParA、Rv1708 和 Rv3213c 和 ParB 的细胞呈丝状和多核体状,表明细胞周期进程存在缺陷。ParA 及其同源物的绿色荧光蛋白融合的可视化显示出类似的定位模式,在极、四分之一细胞、中细胞位置和螺旋状结构处有焦点,表明它们具有功能相关性。另一方面,ParB-GFP 融合蛋白仅定位在细胞极。ParA 和 ParB 的青色和黄色荧光融合蛋白分别在细胞极共定位,表明这些蛋白相互作用,并可能与染色体复制起点相关联。总之,我们的结果表明,结核分枝杆菌 Par 蛋白在细胞周期进程中发挥重要作用。