Asano K, Mizobuchi K
Department of Biophysics and Biochemistry, Graduate School of Science, University of Tokyo, Hongo, Tokyo 113.
EMBO J. 1998 Sep 1;17(17):5201-13. doi: 10.1093/emboj/17.17.5201.
Replication of a low-copy-number IncIalpha plasmid ColIb-P9 depends on expression of the repZ gene encoding the replication initiator protein. repZ expression is negatively controlled by the small antisense Inc RNA, and requires formation of a pseudoknot in the RepZ mRNA consisting of stem-loop I, the Inc RNA target, and a downstream sequence complementary to the loop I. The loop I sequence comprises 5'-rUUGGCG-3', conserved in many prokaryotic antisense systems, and was proposed to be the important site of copy number control. Here we show that the level of repZ expression is rate-limiting for replication and thus copy number, by comparing the levels of repZ expression and copy number from different mutant ColIb-P9 derivatives defective in Inc RNA and pseudoknot formation. Kinetic analyses using in vitro transcribed RNAs indicate that Inc RNA binding and the pseudoknot formation are competitive at the level of initial base paring to loop I. This initial interaction is stimulated by the presence of the loop U residue in the 5'-rUUGGCG-3' motif. These results indicate that the competition between the two RNA-RNA interactions at the specific site is a novel regulatory mechanism for establishing the constant level of repZ expression and thus copy number.
低拷贝数的IncIα质粒ColIb-P9的复制依赖于编码复制起始蛋白的repZ基因的表达。repZ的表达受小分子反义Inc RNA的负调控,并且需要在RepZ mRNA中形成一个假结,该假结由茎环I、Inc RNA靶标以及与环I互补的下游序列组成。环I序列为5'-rUUGGCG-3',在许多原核反义系统中保守,并且被认为是拷贝数控制的重要位点。在这里,我们通过比较来自不同的在Inc RNA和假结形成方面有缺陷的突变ColIb-P9衍生物的repZ表达水平和拷贝数,表明repZ表达水平对复制以及拷贝数而言是限速的。使用体外转录RNA的动力学分析表明,在与环I的初始碱基配对水平上,Inc RNA结合和假结形成是竞争性的。5'-rUUGGCG-3'基序中环U残基的存在刺激了这种初始相互作用。这些结果表明,在特定位点的两种RNA-RNA相互作用之间的竞争是建立repZ表达恒定水平从而确定拷贝数的一种新型调控机制。