A sequence element that tunes Escherichia coli tRNAGGCAla to ensure accurate decoding

被引:77
作者
Ledoux, Sarah [1 ]
Olejniczak, Mikolaj [1 ,2 ]
Uhlenbeck, Olke C. [1 ]
机构
[1] Northwestern Univ, Dept Biochem Mol Biol & Cell Biol, Evanston, IL 60208 USA
[2] Polish Acad Sci, Inst Bioorgan Chem, Poznan, Poland
基金
美国国家卫生研究院;
关键词
AMINOACYL-TRANSFER-RNA; ELONGATION-FACTOR TU; PEPTIDE-BOND FORMATION; 16S RIBOSOMAL-RNA; CODONS IN-VIVO; UNIFORM BINDING; ACTIVE-ROLE; CRYO-EM; ANTICODON; RECOGNITION;
D O I
10.1038/nsmb.1581
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mutating the rare A32-U38 nucleotide pair at the top of the anticodon loop of Escherichia coli tRNA(GGC)(Ala) to a more common U32-A38 pair results in a tRNA that performs almost normally on cognate codons but is unusually efficient in reading near-cognate codons. Pre-steady state kinetic measurements on E. coli ribosomes show that, unlike the wild-type tRNA(GGC)(Ala), the misreading mutant tRNA(GGC)(Ala) shows rapid GTP hydrolysis and no detectable proofreading on near-cognate codons. Similarly, tRNA(GGC)(Ala) mutated to contain C32-G38, a pair that is found in some bacterial tRNA(GGC)(Ala) sequences, was able to decode only the cognate codons, whereas tRNA(GGC)(Ala) containing a more common C32-A38 pair was able to decode all cognate and near-cognate codons tested. We propose that many of the phylogenetically conserved sequence elements present in each tRNA have evolved to suppress translation of near-cognate codons.
引用
收藏
页码:359 / 364
页数:6
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