tRNA 3′ shortening by LCCR4 as a response to stress in Trypanosoma brucei

Author:

Cristodero Marina1ORCID,Brogli Rebecca12,Joss Oliver1,Schimanski Bernd1,Schneider André1,Polacek Norbert1ORCID

Affiliation:

1. Department of Chemistry, Biochemistry and Pharmaceutical Sciences, University of Bern, Freiestrasse 3, 3012 Bern, Switzerland

2. Graduate School for Cellular and Biomedical Sciences, University of Bern, Bern, Switzerland

Abstract

Abstract Sensing of environmental cues is crucial for cell survival. To adapt to changes in their surroundings cells need to tightly control the repertoire of genes expressed at any time. Regulation of translation is key, especially in organisms in which transcription is hardly controlled, like Trypanosoma brucei. In this study, we describe the shortening of the bulk of the cellular tRNAs during stress at the expense of the conserved 3′ CCA-tail. This tRNA shortening is specific for nutritional stress and renders tRNAs unsuitable substrates for translation. We uncovered the nuclease LCCR4 (Tb927.4.2430), a homologue of the conserved deadenylase Ccr4, as being responsible for tRNA trimming. Once optimal growth conditions are restored tRNAs are rapidly repaired by the trypanosome tRNA nucleotidyltransferase thus rendering the recycled tRNAs amenable for translation. This mechanism represents a fast and efficient way to repress translation during stress, allowing quick reactivation with a low energy input.

Funder

Swiss National Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Genetics

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