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噬菌体P1和P7的C4反义RNA前体是大肠杆菌核糖核酸酶P的底物。

Precursor of C4 antisense RNA of bacteriophages P1 and P7 is a substrate for RNase P of Escherichia coli.

作者信息

Hartmann R K, Heinrich J, Schlegl J, Schuster H

机构信息

Abteilung Erdmann, Freie Universität Berlin, Germany.

出版信息

Proc Natl Acad Sci U S A. 1995 Jun 20;92(13):5822-6. doi: 10.1073/pnas.92.13.5822.

Abstract

The C4 repressor of the temperate bacteriophages P1 and P7 inhibits antirepressor (Ant) synthesis and is essential for establishment and maintenance of lysogeny. C4 is an antisense RNA acting on a target, Ant mRNA, which is transcribed from the same promoter. The antisense-target RNA interaction requires processing of C4 RNA from a precursor RNA. Here we show that 5' maturation of C4 RNA in vivo depends on RNase P. In vitro, Escherichia coli RNase P and its catalytic RNA subunit (M1 RNA) can generate the mature 5' end of C4 RNA from P1 by a single endonucleolytic cut, whereas RNase P from the E. coli rnpA49 mutant, carrying a missense mutation in the RNase P protein subunit, is defective in the 5' maturation of C4 RNA. Primer extension analysis of RNA transcribed in vivo from a plasmid carrying the P1 c4 gene revealed that 5'-mature C4 RNA was the predominant species in rnpA+ bacteria, whereas virtually no mature C4 RNA was found in the temperature-sensitive rnpA49 strain at the restrictive temperature. Instead, C4 RNA molecules carrying up to five extra nucleotides beyond the 5' end accumulated. The same phenotype was observed in rnpA+ bacteria which harbored a plasmid carrying a P7 c4 mutant gene with a single C-->G base substitution in the structural homologue to the CCA 3' end of tRNAs. Implications of C4 RNA processing for the lysis/lysogeny decision process of bacteriophages P1 and P7 are discussed.

摘要

温和噬菌体P1和P7的C4阻遏物可抑制抗阻遏物(Ant)的合成,对于溶原状态的建立和维持至关重要。C4是一种反义RNA,作用于从同一启动子转录而来的靶标Ant mRNA。反义-靶标RNA相互作用需要从前体RNA加工C4 RNA。在此我们表明,C4 RNA在体内的5'端成熟依赖于核糖核酸酶P。在体外,大肠杆菌核糖核酸酶P及其催化RNA亚基(M1 RNA)可通过一次内切核酸酶切割从P1产生成熟的C4 RNA的5'端,而来自大肠杆菌rnpA49突变体的核糖核酸酶P在核糖核酸酶P蛋白亚基中携带错义突变,在C4 RNA的5'端成熟过程中存在缺陷。对携带P1 c4基因的质粒在体内转录的RNA进行引物延伸分析表明,5'-成熟的C4 RNA是rnpA+细菌中的主要种类,而在温度敏感的rnpA49菌株处于限制温度时几乎未发现成熟的C4 RNA。相反,在5'端携带多达五个额外核苷酸的C4 RNA分子积累。在携带P7 c4突变基因的质粒的rnpA+细菌中也观察到相同表型,该突变基因在与tRNA的CCA 3'端结构同源物中的单个C→G碱基替换。讨论了C4 RNA加工对噬菌体P1和P7的裂解/溶原决定过程的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04a4/41593/bceca0af7534/pnas01489-0071-a.jpg

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