Common location of determinants in initiator transfer RNAs for initiator-elongator discrimination in bacteria and in eukaryotes

Stortchevoi, Alexei ; Varshney, Umesh ; RajBhandary, Uttam L. (2003) Common location of determinants in initiator transfer RNAs for initiator-elongator discrimination in bacteria and in eukaryotes The Journal of Biological Chemistry, 278 (20). pp. 17672-17679. ISSN 0021-9258

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Official URL: http://www.jbc.org/content/278/20/17672.abstract?s...

Related URL: http://dx.doi.org/10.1074/jbc.M212890200

Abstract

Initiator tRNAs are used exclusively for initiation of protein synthesis and not for elongation. We show that both Escherichia coli and eukaryotic initiator tRNAs have negative determinants, at the same positions, that block their activity in elongation. The primary negative determinant in E. coliinitiator tRNA is the C1xA72 mismatch at the end of the acceptor stem. The primary negative determinant in eukaryotic initiator tRNAs is located in the Tψ C stem, whereas a secondary negative determinant is the A1:U72 base pair at the end of the acceptor stem. Here we show thatE. coli initiator tRNA also has a secondary negative determinant for elongation and that it is the U50·G64 wobble base pair, located at the same position in the Tψ C stem as the primary negative determinant in eukaryotic initiator tRNAs. Mutation of the U50·G64 wobble base pair to C50:G64 or U50:A64 base pairs increases the in vivo amber suppressor activity of initiator tRNA mutants that have changes in the acceptor stem and in the anticodon sequence necessary for amber suppressor activity. Binding assays of the mutant aminoacyl-tRNAs carrying the C50 and A64 changes to the elongation factor EF-Tu·GTP show marginally higher affinity of the C50 and A64 mutant tRNAs and increased stability of the EF-Tu·GTP· aminoacyl-tRNA ternary complexes. Other results show a large effect of the amino acid attached to a tRNA, glutamineversus methionine, on the binding affinity toward EF-Tu·GTP and on the stability of the EF-Tu·GTP·aminoacyl-tRNA ternary complex.

Item Type:Article
Source:Copyright of this article belongs to American Society for Biochemistry and Molecular Biology.
ID Code:56243
Deposited On:23 Aug 2011 11:54
Last Modified:23 Aug 2011 11:54

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