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Dual function of the tRNA(m5U54)methyltransferase in tRNA maturation

Published online by Cambridge University Press:  24 April 2002

MARCUS J.O. JOHANSSON  and
ANDERS S. BYSTRÖM
MARCUS J.O. JOHANSSON
Affiliation:
Department of Molecular Biology, Umeå University, 901 87 Umeå, Sweden
ANDERS S. BYSTRÖM
Affiliation:
Department of Molecular Biology, Umeå University, 901 87 Umeå, Sweden
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Abstract

A 5-methyluridine (m5U) residue at position 54 is a conserved feature of bacterial and eukaryotic tRNAs. The methylation of U54 is catalyzed by the tRNA(m5U54)methyltransferase, which in Saccharomyces cerevisiae is encoded by the nonessential TRM2 gene. In this study, we identified four different strains with mutant forms of tRNACGASer. The absence of the TRM2 gene in these strains decreased the stability of tRNACGASer and induced lethality. Two alleles of TRM2 encoding catalytically inactive tRNA(m5U54)methyltransferases were able to stabilize tRNACGASer in one of the mutants, revealing a role for the Trm2 protein per se in tRNA maturation. Other tRNA modification enzymes interacting with tRNACGASer in the maturation process, such as Pus4p, Trm1p, and Trm3p were essential or important for growth of the tRNACGASer mutants. Moreover, Lhp1p, a protein binding RNA polymerase III transcripts, was required to stabilize the mutant tRNAs. Based on our results, we suggest that tRNA modification enzymes might have a role in tRNA maturation not necessarily linked to their known catalytic activity.

Keywords

5-methyluridineLHP1PUS4sup61TRM1TRM2TRM3tRNA maturation
Type
Research Article
Information
RNA , Volume 8 , Issue 3 , March 2002 , pp. 324 - 335
Copyright
© 2002 RNA Society

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