Endonucleolytic processing of CCA-less tRNA precursors by RNase Z in Bacillus subtilis

被引:103
作者
Pellegrini, O
Nezzar, J
Marchfelder, A
Putzer, H
Condon, C
机构
[1] CNRS, Inst Biol Physiochim, UPR 9073, F-75005 Paris, France
[2] Univ Ulm, D-89069 Ulm, Germany
关键词
CCA; endonuclease; tRNA; RNase Z; 3 ' tRNase;
D O I
10.1093/emboj/cdg435
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In contrast to Escherichia coli, where the 3' ends of tRNAs are primarily generated by exoribonucleases, maturation of the 3' end of tRNAs is catalysed by an endoribonuclease, known as RNase Z (or 3' tRNase), in many eukaryotic and archaeal systems. RNase Z cleaves tRNA precursors 3' to the discriminator base. Here we show that this activity, previously unsuspected in bacteria, is encoded by the yqjK gene of Bacillus subtilis. Decreased yqjK expression leads to an accumulation of a population of B.subtilis tRNAs in vivo, none of which have a CCA motif encoded in their genes, and YqjK cleaves tRNA precursors with the same specificity as plant RNase Z in vitro. We have thus renamed the gene rnz. A CCA motif downstream of the discriminator base inhibits RNase Z activity in vitro, with most of the inhibition due to the first C residue. Lastly, tRNAs with long 5' extensions are poor substrates for cleavage, suggesting that for some tRNAs, processing of the 5' end by RNase P may have to precede RNase Z cleavage.
引用
收藏
页码:4534 / 4543
页数:10
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