del Solar G, Acebo P, Espinosa M
Centro de Investigaciones Biológicas, CSIC, Madrid, Spain.
Mol Microbiol. 1997 Jan;23(1):95-108. doi: 10.1046/j.1365-2958.1997.1981561.x.
Replication of the streptococcal plasmid pLS1 is controlled by two plasmid-encoded gene products: the repressor protein CopG and the antisense RNA, RNA II. Two different mutants in rnaII have been isolated. The 5'-end and the levels of RNA II synthesized by pneumococcal cells harbouring the wild-type pLS1 or mutant plasmids (affected in either genes copG or rnaII) were analysed. One of the rnaII mutants exhibited a high-copy-number phenotype, whereas an in vitro-constructed mutation, which affects the -10 region of the rnaII promoter, resulted in plasmids lacking copy-number phenotype. The latter mutation had a pleiotropic effect: It abolished RNA II synthesis, but it also affected the initiation of translation signals of the gene encoding the RepB initiator protein. Transcriptional and translational fusions, together with in vitro inhibition of RepB synthesis by specific oligonucleotides, showed translational inhibition of RepB synthesis by RNA II, perhaps by directly blocking the accessibility of the ribosomes to the repB initiation of translation signals.
链球菌质粒pLS1的复制受两种质粒编码基因产物控制:阻遏蛋白CopG和反义RNA即RNA II。已分离出rnaII的两种不同突变体。分析了携带野生型pLS1或突变质粒(copG或rnaII基因受影响)的肺炎球菌细胞合成的RNA II的5′端和水平。其中一个rnaII突变体表现出高拷贝数表型,而一个影响rnaII启动子-10区的体外构建突变导致质粒缺乏拷贝数表型。后一种突变具有多效性:它消除了RNA II的合成,但也影响了编码RepB起始蛋白基因的翻译起始信号。转录和翻译融合,以及特定寡核苷酸对RepB合成的体外抑制,表明RNA II对RepB合成有翻译抑制作用,可能是通过直接阻止核糖体接近repB翻译起始信号。