Kim Kwang-Sun, Sim Soyeong, Ko Jae-Hyeong, Lee Younghoon
Department of Chemistry and Center for Molecular Design and Synthesis, Korea Advanced Institute of Science and Technology, Daejeon 305-701, Korea.
J Biol Chem. 2005 Oct 14;280(41):34667-74. doi: 10.1074/jbc.M505005200. Epub 2005 Aug 15.
M1 RNA, the catalytic subunit of Escherichia coli RNase P, is an essential ribozyme that processes the 5' leader sequence of precursor tRNAs. It is generated by the removal of 36 nucleotides from the 3' end of the primary rnpB transcript (pM1 RNA), but the biological significance of this reaction in bacterial metabolism remains obscure. In this study, we constructed and analyzed bacterial strains carrying mutations in the rne-dependent site of their rnpB genes, showing that the 3' processing of M1 RNA is essential for cell viability. Furthermore, we demonstrate that pM1 RNA can undergo not only 3' processing but also poly(A)-dependent degradation. Therefore, our results suggest that the 3' processing of M1 RNA provides a functional mechanism for the protection of its primary transcript against degradation.
M1 RNA是大肠杆菌核糖核酸酶P的催化亚基,是一种重要的核酶,可加工前体tRNA的5'前导序列。它是通过从初级rnpB转录本(pM1 RNA)的3'末端去除36个核苷酸而产生的,但该反应在细菌代谢中的生物学意义仍不清楚。在本研究中,我们构建并分析了rnpB基因的rne依赖位点携带突变的细菌菌株,表明M1 RNA的3'加工对于细胞活力至关重要。此外,我们证明pM1 RNA不仅可以进行3'加工,还可以进行多聚腺苷酸依赖性降解。因此,我们的结果表明,M1 RNA的3'加工为保护其初级转录本不被降解提供了一种功能机制。