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大肠杆菌中一种新型核糖核酸内切酶RNase LS。

A novel endoribonuclease, RNase LS, in Escherichia coli.

作者信息

Otsuka Yuichi, Yonesaki Tetsuro

机构信息

Department of Biology, Graduate School of Science, Osaka University, Osaka 560-0043, Japan.

出版信息

Genetics. 2005 Jan;169(1):13-20. doi: 10.1534/genetics.104.033290.

Abstract

The dmd gene of bacteriophage T4 is required for the stability of late-gene mRNAs. When this gene is mutated, late genes are globally silenced because of rapid degradation of their mRNAs. Our previous work suggested that a novel Escherichia coli endonuclease, RNase LS, is responsible for the rapid degradation of mRNAs. In this study, we demonstrated that rnlA (formerly yfjN) is essential for RNase LS activity both in vivo and in vitro. In addition, we investigated a role of RNase LS in the RNA metabolism of E. coli cells under vegetative growth conditions. A mutation in rnlA reduced the decay rate of many E. coli mRNAs, although there are differences in the mutational effects on the stabilization of different mRNAs. In addition, we found that a 307-nucleotide fragment with an internal sequence of 23S rRNA accumulated to a high level in rnlA mutant cells. These results strongly suggest that RNase LS plays a role in the RNA metabolism of E. coli as well as phage T4.

摘要

噬菌体T4的dmd基因是晚期基因mRNA稳定性所必需的。当该基因发生突变时,晚期基因会因mRNA的快速降解而整体沉默。我们之前的工作表明,一种新型的大肠杆菌内切核酸酶RNase LS负责mRNA的快速降解。在本研究中,我们证明rnlA(以前称为yfjN)在体内和体外对RNase LS活性都是必不可少的。此外,我们研究了RNase LS在大肠杆菌细胞营养生长条件下RNA代谢中的作用。rnlA突变降低了许多大肠杆菌mRNA的降解速率,尽管不同mRNA的稳定化突变效应存在差异。此外,我们发现一个具有23S rRNA内部序列的307个核苷酸片段在rnlA突变细胞中积累到高水平。这些结果有力地表明,RNase LS在大肠杆菌以及噬菌体T4的RNA代谢中发挥作用。

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