4.8 Article

Drosophila RNase Z processes mitochondrial and nuclear pre-tRNA 3 ' ends in vivo

Journal

NUCLEIC ACIDS RESEARCH
Volume 32, Issue 1, Pages 255-262

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkh182

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Funding

  1. NIGMS NIH HHS [T34GM08498, SO6GM08153, T34 GM008498, S06 GM008153] Funding Source: Medline
  2. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [T34GM008498, S06GM008153] Funding Source: NIH RePORTER

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Although correct tRNA 3' ends are crucial for protein biosynthesis, generation of mature tRNA 3' ends in eukaryotes is poorly understood and has so far only been investigated in vitro. We report here for the first time that eukaryotic tRNA 3' end maturation is catalysed by the endonuclease RNase Z in vivo. Silencing of the JhI-1 gene (RNase Z homolog) in vivo with RNAi in Drosophila S2 cultured cells causes accumulation of nuclear and mitochondrial pre-tRNAs, suggesting that JhI-1 encodes both forms of the tRNA 3' endonuclease RNase Z, and establishing its biological role in endonucleolytic tRNA 3' end processing. In addition our data show that in vivo 5' processing of nuclear and mitochondrial pre-tRNAs occurs before 3' processing.

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