Functional characterization of the human tRNA methyltransferases TRMT10A and TRMT10B

Author:

Vilardo Elisa1ORCID,Amman Fabian2ORCID,Toth Ursula1,Kotter Annika3,Helm Mark3ORCID,Rossmanith Walter1ORCID

Affiliation:

1. Center for Anatomy & Cell Biology, Medical University of Vienna, 1090 Vienna, Austria

2. Department of Theoretical Chemistry, University of Vienna, 1090 Vienna, Austria

3. Institute for Pharmacy and Biochemistry, Johannes Gutenberg-University, 55128 Mainz, Germany

Abstract

Abstract The TRM10 family of methyltransferases is responsible for the N1-methylation of purines at position 9 of tRNAs in Archaea and Eukarya. The human genome encodes three TRM10-type enzymes, of which only the mitochondrial TRMT10C was previously characterized in detail, whereas the functional significance of the two presumably nuclear enzymes TRMT10A and TRMT10B remained unexplained. Here we show that TRMT10A is m1G9-specific and methylates a subset of nuclear-encoded tRNAs, whilst TRMT10B is the first m1A9-specific tRNA methyltransferase found in eukaryotes and is responsible for the modification of a single nuclear-encoded tRNA. Furthermore, we show that the lack of G9 methylation causes a decrease in the steady-state levels of the initiator tRNAiMet-CAT and an alteration in its further post-transcriptional modification. Our work finally clarifies the function of TRMT10A and TRMT10B in vivo and provides evidence that the loss of TRMT10A affects the pool of cytosolic tRNAs required for protein synthesis.

Funder

Austrian Science Fund

German Research Foundation

FWF

Publisher

Oxford University Press (OUP)

Subject

Genetics

Reference44 articles.

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