Asano K, Hama C, Inoue S, Moriwaki H, Mizobuchi K
Department of Biophysics and Biochemistry, Graduate School of Science, University of Tokyo, Hongo, Tokyo 113, Japan.
J Biol Chem. 1999 Jun 18;274(25):17924-33. doi: 10.1074/jbc.274.25.17924.
The autonomous replication region of plasmid ColIb-P9 contains repZ encoding the RepZ replication protein, and inc and repY as the negative and positive regulators of repZ translation, respectively. inc encodes the antisense Inc RNA, and repY is a short open reading frame upstream of repZ. Translation of repY enables repZ translation by inducing formation of a pseudoknot containing stem-loop I, which base pairs with the sequence preceding the repZ start codon. Inc RNA inhibits both repY translation and formation of the pseudoknot by binding to the loop I. To investigate control of repY expression by Inc RNA, we isolated a number of mutations that express repY in the presence of Inc RNA. One class of mutations delete a part of another stem-loop (II), which derepresses repY expression by initiating translation at codon 10 (GUG), located within this structure. Point mutations in stem-loop II can also derepress repY translation, and the introduction of compensatory base-changes restores control of repY translation. These results not only indicate that suppressing a cryptic start codon by secondary structure is important for maintaining the translational control of repZ but also demonstrate that the position of start site for repY translation is critical for its control by Inc RNA. Thus, Inc RNA controls repY translation by binding in the vicinity of the start codon, in contrast to the control of repZ expression at the level of loop-loop interaction.
质粒ColIb-P9的自主复制区域包含编码RepZ复制蛋白的repZ,以及分别作为repZ翻译的负调控因子和正调控因子的inc和repY。inc编码反义Inc RNA,repY是repZ上游的一个短开放阅读框。repY的翻译通过诱导形成包含茎环I的假结来实现repZ的翻译,该假结与repZ起始密码子之前的序列碱基配对。Inc RNA通过与环I结合来抑制repY的翻译和假结的形成。为了研究Inc RNA对repY表达的调控,我们分离出了一些在Inc RNA存在时仍能表达repY的突变。一类突变缺失了另一个茎环(II)的一部分,通过在该结构内的密码子10(GUG)处起始翻译来解除对repY表达的抑制。茎环II中的点突变也能解除对repY翻译的抑制,引入补偿性碱基变化可恢复对repY翻译的调控。这些结果不仅表明通过二级结构抑制一个隐蔽的起始密码子对于维持repZ的翻译调控很重要,还证明了repY翻译起始位点的位置对于其受Inc RNA调控至关重要。因此,与在环-环相互作用水平对repZ表达的调控相反,Inc RNA通过在起始密码子附近结合来控制repY的翻译。