Wilson I W, Praszkier J, Pittard A J
Department of Microbiology, University of Melbourne, Parkville, Victoria, Australia.
J Bacteriol. 1994 Nov;176(21):6497-508. doi: 10.1128/jb.176.21.6497-6508.1994.
The translation of RepA, the replication initiation protein of the IncB plasmid pMU720, requires that its mRNA (RNAII) folds to form a pseudoknot immediately upstream of the repA Shine-Dalgarno sequence. The formation of this pseudoknot is dependent in turn on the translation and correct termination of a leader peptide, RepB. A small countertranscript RNA, RNAI, controls the replication of pMU720 by interacting with RNAII to negatively regulate the expression of repA both directly, by sequestering the proximal bases required for pseudoknot formation, and indirectly, by inhibiting the translation of repB. Inhibition of the translation of repB by RNAI was found to depend on the close proximity of the RNAI-RNAII complex to the translational initiation region of repB, indicating that the primary mechanism of RNAI control involves steric hindrance. Disruption of RNAI control of repB had only a small effect on the copy number of the IncB plasmid, indicating that inhibition of the expression of repA by RNAI is achieved predominantly by inhibition of pseudoknot formation rather than by inhibition of repB translation.
IncB质粒pMU720的复制起始蛋白RepA的翻译,要求其信使核糖核酸(RNAII)折叠形成一个假结,该假结位于repA的夏因-达尔加诺序列上游紧邻处。这个假结的形成反过来又依赖于前导肽RepB的翻译及正确终止。一个小的反式转录RNA,即RNAI,通过与RNAII相互作用来控制pMU720的复制,它直接通过隔离假结形成所需的近端碱基、间接通过抑制repB的翻译来负向调节repA的表达。发现RNAI对repB翻译的抑制依赖于RNAI-RNAII复合物与repB翻译起始区域的紧密接近,这表明RNAI控制的主要机制涉及空间位阻。RNAI对repB的控制被破坏对IncB质粒的拷贝数只有很小的影响,这表明RNAI对repA表达的抑制主要是通过抑制假结形成而非通过抑制repB翻译来实现的。