Identification of RNA helicases with unwinding activity on angiogenin-processed tRNAs

Author:

Drino Aleksej1,König Lisa1,Capitanchik Charlotte2,Sanadgol Nasim1,Janisiw Eva1,Rappol Tom1,Vilardo Elisa1ORCID,Schaefer Matthias R1ORCID

Affiliation:

1. Division of Cell and Developmental Biology, Center for Anatomy and Cell Biology, Medical University of Vienna , Schwarzspanierstr. 17-I, A-1090 Vienna , Austria

2. RNA Networks Laboratory, Francis Crick Institute , London , UK

Abstract

AbstractStress-induced tRNA fragmentation upon environmental insult is a conserved cellular process catalysed by endonucleolytic activities targeting mature tRNAs. The resulting tRNA-derived small RNAs (tsRNAs) have been implicated in various biological processes that impact cell-to-cell signalling, cell survival as well as gene expression regulation during embryonic development. However, how endonuclease-targeted tRNAs give rise to individual and potentially biologically active tsRNAs remains poorly understood. Here, we report on the in vivo identification of proteins associated with stress-induced tsRNAs-containing protein complexes, which, together with a ‘tracer tRNA’ assay, were used to uncover enzymatic activities that can bind and process specific endonuclease-targeted tRNAs in vitro. Among those, we identified conserved ATP-dependent RNA helicases which can robustly separate tRNAs with endonuclease-mediated ‘nicks’ in their anticodon loops. These findings shed light on the existence of cellular pathways dedicated to producing individual tsRNAs after stress-induced tRNA hydrolysis, which adds to our understanding as to how tRNA fragmentation and the resulting tsRNAs might exert physiological impact.

Funder

Austrian Science Fund

Publisher

Oxford University Press (OUP)

Subject

Genetics

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