Your browser doesn't support javascript.
loading
Drop-off-reinitiation at the amino termini of nascent peptides and its regulation by IF3, EF-G, and RRF.
Katoh, Takayuki; Suga, Hiroaki.
Afiliación
  • Katoh T; Department of Chemistry, Graduate School of Science, The University of Tokyo, Bunkyo-ku, Tokyo 113-0033, Japan katoh@chem.s.u-tokyo.ac.jp hsuga@chem.s.u-tokyo.ac.jp.
  • Suga H; Department of Chemistry, Graduate School of Science, The University of Tokyo, Bunkyo-ku, Tokyo 113-0033, Japan katoh@chem.s.u-tokyo.ac.jp hsuga@chem.s.u-tokyo.ac.jp.
RNA ; 29(5): 663-674, 2023 05.
Article en En | MEDLINE | ID: mdl-36754577
In translation initiation in prokaryotes, IF3 recognizes the interaction between the initiator codon of mRNA and the anticodon of fMet-tRNAini and then relocates the fMet-tRNAini to an active position. Here, we have surveyed 328 codon-anticodon combinations for the preference of IF3. At the first and second base of the codon, only Watson-Crick base pairs are tolerated. At the third base, stronger base pairs, for example, Watson-Crick, are more preferred, but other types of base pairs, for example, G/U wobble, are also tolerated; weaker base pairs are excluded by IF3. When the codon-anticodon combinations are unfavorable for IF3 or the concentration of IF3 is too low to recognize any codon-anticodon combinations, IF3 fails to set the P-site fMet-tRNAini at the active position and causes its drop-off from the ribosome. Thereby, translation reinitiation occurs from the second aminoacyl-tRNA at the A site to yield a truncated peptide lacking the amino-terminal fMet. We refer to this event as the amino-terminal drop-off-reinitiation. We also showed that EF-G and RRF are involved in disassembling such an aberrant ribosome complex bearing inactive fMet-tRNAini Thereby EF-G and RRF are able to exclude unfavorable codon-anticodon combinations with weaker base pairs and alleviate the amino-terminal drop-off-reinitiation.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Iniciación de la Cadena Peptídica Traduccional / Factor G de Elongación Peptídica Idioma: En Revista: RNA Asunto de la revista: BIOLOGIA MOLECULAR Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Iniciación de la Cadena Peptídica Traduccional / Factor G de Elongación Peptídica Idioma: En Revista: RNA Asunto de la revista: BIOLOGIA MOLECULAR Año: 2023 Tipo del documento: Article