Studies of translational misreading in vivo show that the ribosome very efficiently discriminates against most potential errors

RNA. 2014 Jan;20(1):9-15. doi: 10.1261/rna.039792.113. Epub 2013 Nov 18.

Abstract

Protein synthesis must rapidly and repeatedly discriminate between a single correct and many incorrect aminoacyl-tRNAs. We have attempted to measure the frequencies of all possible missense errors by tRNA , tRNA and tRNA . The most frequent errors involve three types of mismatched nucleotide pairs, U•U, U•C, or U•G, all of which can form a noncanonical base pair with geometry similar to that of the canonical U•A or C•G Watson-Crick pairs. Our system is sensitive enough to measure errors at other potential mismatches that occur at frequencies as low as 1 in 500,000 codons. The ribosome appears to discriminate this efficiently against any pair with non-Watson-Crick geometry. This extreme accuracy may be necessary to allow discrimination against the errors involving near Watson-Crick pairing.

Keywords: Escherichia coli; mistranslation; non-Watson–Crick base pairs; protein synthesis; β-galactosidase.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amino Acid Substitution
  • Base Pair Mismatch / physiology*
  • Base Pairing / physiology
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Mutagenesis / physiology
  • Mutation, Missense* / physiology
  • Nucleic Acid Conformation
  • Organisms, Genetically Modified
  • Protein Biosynthesis / physiology*
  • RNA, Transfer, Asp / metabolism
  • RNA, Transfer, Glu / metabolism
  • RNA, Transfer, Tyr / metabolism
  • Ribosomes / physiology*
  • beta-Galactosidase / chemistry
  • beta-Galactosidase / genetics
  • beta-Galactosidase / metabolism

Substances

  • RNA, Transfer, Asp
  • RNA, Transfer, Glu
  • RNA, Transfer, Tyr
  • beta-Galactosidase