PMID:9642056
| Citation |
O'Connor, M (1998) tRNA imbalance promotes -1 frameshifting via near-cognate decoding. J. Mol. Biol. 279:727-36 |
|---|---|
| Abstract |
tRNAGly1 is the Escherichia coli glycine tRNA specific for GGG codons. A genetic selection for multicopy suppressors of a frameshift mutation has shown that increased levels of wild-type tRNAGly1 causes -1 frameshifting. Analysis of the suppression spectrum of this multicopy suppressor and peptide sequencing of the suppressed protein product showed that it promoted GG doublet decoding at the near-cognate GGA codons. It is proposed that increasing the concentration of the GGG-specific tRNAGly1 relative to the cognate GGA-decoding tRNAGly2 allows the near-cognate tRNA to read GGA codons. Near-cognate decoding of GGA codons by tRNAGly1 can occur by a two-out-of-three reading mechanism, in which only the first two bases of the GGA codon are paired with the anticodon, thus permitting doublet translocations. In mycoplasmas, a single tRNA typically decodes all four triplets of a codon family and introduction of a feature of the Mypoplasma mycoides tRNAGly responsible for non-discriminate decoding, a C at position 32, into the anticodon E. coli tRNAGly1, enhanced the efficiency of doublet decoding. |
| Links |
PubMed Online version:10.1006/jmbi.1998.1832 |
| Keywords |
Escherichia coli/genetics; Frameshift Mutation; Gene Expression Regulation, Bacterial; Protein Biosynthesis; RNA, Bacterial/genetics; RNA, Transfer, Gly/genetics |
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