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质粒ColIb-P9 Inc RNA与其靶RNA形成的晚期中间体复合物的结构分析。单个反义RNA如何以不同速率抑制两个基因的翻译?

Structural analysis of late intermediate complex formed between plasmid ColIb-P9 Inc RNA and its target RNA. How does a single antisense RNA repress translation of two genes at different rates?

作者信息

Asano K, Mizobuchi K

机构信息

Department of Biophysics and Biochemistry, Graduate School of Science, University of Tokyo, Hongo, Tokyo 113-0033, Japan.

出版信息

J Biol Chem. 2000 Jan 14;275(2):1269-74. doi: 10.1074/jbc.275.2.1269.

Abstract

The antisense Inc RNA encoded by the IncIalpha ColIb-P9 plasmid replicon controls the translation of repZ encoding the replication initiator and its leader peptide repY at different rates with different mechanisms. The initial loop-loop base pairing between Inc RNA and the target in the repZ mRNA leader inhibits formation of a pseudoknot required for repZ translation. A subsequent base pairing at the 5' leader of Inc RNA blocks repY translation. To delineate the molecular basis for the differential control, we analyzed the intermediate complexes formed between RepZ mRNA and Inc RNA(54), a 5'-truncated Inc RNA derivative. We found that the initial base pairing at the loops transforms into a more stable intermediate complex by its propagation in both directions. The resulting extensive base pairing indicates that the inhibition of the pseudoknot formation is established at this stage. Furthermore, the region of extensive base pairing includes bases different in related plasmids showing different incompatibility. Thus, the observed extensive base pairing is important for determining the incompatibility of the low-copy-number plasmids. We discuss the evolution of replication control systems found in IncIalpha, IncB, and IncFII group plasmids.

摘要

由IncIα ColIb - P9质粒复制子编码的反义Inc RNA以不同机制、不同速率控制编码复制起始蛋白的repZ及其前导肽repY的翻译。Inc RNA与repZ mRNA前导区中的靶标之间最初的环 - 环碱基配对会抑制repZ翻译所需假结的形成。随后,Inc RNA 5'前导区的碱基配对会阻断repY的翻译。为了阐明这种差异控制的分子基础,我们分析了RepZ mRNA与Inc RNA(54)(一种5'端截短的Inc RNA衍生物)之间形成的中间复合物。我们发现,环处最初的碱基配对通过向两个方向延伸而转变为更稳定的中间复合物。由此产生的广泛碱基配对表明,假结形成的抑制在此阶段就已确立。此外,广泛碱基配对区域包含相关质粒中不同的碱基,这些质粒表现出不同的不相容性。因此,观察到的广泛碱基配对对于确定低拷贝数质粒的不相容性很重要。我们讨论了在IncIα、IncB和IncFII组质粒中发现的复制控制系统的进化。

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