Genes Dev. 2001 September 1; 15(17): 2295–2306.

  1. Damien Brégeon1,4,
  2. Vincent Colot2,3,
  3. Miroslav Radman1, and
  4. François Taddei1

+ Author Affiliations

  1. 1INSERM EPI9916, Faculté de Médecine Necker-Enfants Malades, 75730 Paris Cedex 15, France; 2Institut Jacques Monod, CNRS-Universités Paris 6 et Paris 7, 75251 Paris Cedex 05, France




Errors during gene expression from DNA to proteins via transcription and translation may be deleterious for the functional maintenance of cells. In this paper, extensive genetic studies of the misreading of a GA repeat introduced into the lacZ gene of Escherichia coli indicate that in this bacteria, errors occur predominantly by a +2 translational frameshift, which is controlled by a tRNA modification involving the MnmE and GidA proteins. This ribosomal frameshift results from the coincidence of three events: (1) decreased codon–anticodon affinity at the P-site, which is caused by tRNA hypomodification in mnmE andgidA strains; (2) a repetitive mRNA sequence predisposing to slippage; and (3) increased translational pausing attributable to the presence of a rare codon at the A-site. Based on genetic analysis, we propose that GidA and MnmE act in the same pathway of tRNA modification, the absence of which is responsible for the +2 translational frameshift. The difference in the impact of the mutant gene on cell growth, however, indicates that GidA has at least one other function.



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