Literature DB >> 12003492

Dual function of the tRNA(m(5)U54)methyltransferase in tRNA maturation.

Marcus J O Johansson1, Anders S Byström.   

Abstract

A 5-methyluridine (m(5)U) 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 tRNA(Ser)CGA. The absence of the TRM2 gene in these strains decreased the stability of tRNA(Ser)CGA and induced lethality. Two alleles of TRM2 encoding catalytically inactive tRNA(m5U54)methyltransferases were able to stabilize tRNA(Ser)CGA in one of the mutants, revealing a role for the Trm2 protein per se in tRNA maturation. Other tRNA modification enzymes interacting with tRNA(Ser)CGA in the maturation process, such as Pus4p, Trm1 p, and Trm3p were essential or important for growth of the tRNA(Ser)CGA 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.

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Year:  2002        PMID: 12003492      PMCID: PMC1370254          DOI: 10.1017/s1355838202027851

Source DB:  PubMed          Journal:  RNA        ISSN: 1355-8382            Impact factor:   4.942


  39 in total

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Journal:  Biochemistry       Date:  1991-10-08       Impact factor: 3.162

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  48 in total

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Journal:  RNA       Date:  2006-04       Impact factor: 4.942

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8.  Chapter 11. Identification and analysis of tRNAs that are degraded in Saccharomyces cerevisiae due to lack of modifications.

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Journal:  Methods Enzymol       Date:  2008       Impact factor: 1.600

9.  A new nuclear function of the Entamoeba histolytica glycolytic enzyme enolase: the metabolic regulation of cytosine-5 methyltransferase 2 (Dnmt2) activity.

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Authors:  Mark A Bayfield; Richard J Maraia
Journal:  Nat Struct Mol Biol       Date:  2009-03-15       Impact factor: 15.369

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