Maturation of the 5′ end of Bacillus subtilis 16S rRNA by the essential ribonuclease YkqC/RNase J1

被引:124
作者
Britton, Robert A.
Wen, Tingyi
Schaefer, Laura
Pellegrini, Olivier
Uicker, William C.
Mathy, Nathalie
Tobin, Crystal
Daou, Roula
Szyk, Jacek
Condon, Ciaran
机构
[1] Univ Paris 07, CNRS, UPR 9073, Inst Biol Physicochim, F-75005 Paris, France
[2] Michigan State Univ, Dept Microbiol & Mol Genet, E Lansing, MI 48824 USA
关键词
D O I
10.1111/j.1365-2958.2006.05499.x
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
Functional ribosomal RNAs are generated from longer precursor species in every organism known. Maturation of the 5' side of 16S rRNA in Escherichia coli is catalysed in a two-step process by the cooperative action of RNase E and RNase G. However, many bacteria lack RNase E and RNase G orthologues, raising the question as to how 16S rRNA processing occurs in these organisms. Here we show that the maturation of Bacillus subtilis 16S rRNA is also a two-step process and that the enzyme responsible for the generation of the mature 5' end is the widely distributed essential ribonuclease YkqC/RNase J1. Depletion of B. subtilis of RNase J1 results in an accumulation of 16S rRNA precursors in vivo. The precursor species are found in polysomes suggesting that they can function in translation. Mutation of the predicted catalytic site of RNase J1 abolishes both 16S rRNA processing and cell viability. Finally, purified RNase J1 can correctly mature precursor 16S rRNA assembled in 70S ribosomes, showing that its role is direct.
引用
收藏
页码:127 / 138
页数:12
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