z-logo
Premium
Endonucleolytic processing of CCA‐less tRNA precursors by RNase Z in Bacillus subtilis
Author(s) -
Pellegrini Olivier,
Nezzar Jamel,
Marchfelder Anita,
Putzer Harald,
Condon Ciarán
Publication year - 2003
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1093/emboj/cdg435
Subject(s) - biology , bacillus subtilis , rnase p , transfer rna , genetics , bacillaceae , computational biology , rna , bacteria , gene
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.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom