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Chemical and structural characterization of a model Post-Termination Complex (PoTC) for the ribosome recycling reaction: Evidence for the release of the mRNA by RRF and EF-G.
Iwakura, Nobuhiro; Yokoyama, Takeshi; Quaglia, Fabio; Mitsuoka, Kaoru; Mio, Kazuhiro; Shigematsu, Hideki; Shirouzu, Mikako; Kaji, Akira; Kaji, Hideko.
Afiliação
  • Iwakura N; Department of Biochemistry and Molecular Biology, Thomas Jefferson University, Jefferson Medical College, Philadelphia, Pennsylvania, United States of America.
  • Yokoyama T; Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
  • Quaglia F; Division of Structural and Synthetic Biology, RIKEN Center for Life Science Technologies, Yokohama, Japan.
  • Mitsuoka K; Department of Biochemistry and Molecular Biology, Thomas Jefferson University, Jefferson Medical College, Philadelphia, Pennsylvania, United States of America.
  • Mio K; Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America.
  • Shigematsu H; University of Camerino, School of Biosciences and Veterinary Medicine, Camerino, Italy.
  • Shirouzu M; Research Center for Ultra-High Voltage Electron Microscopy, Osaka University, Osaka, Japan.
  • Kaji A; Molecular Profiling Research Center for Drug Discovery and OPERANDO Open Innovation Laboratory, National Institute of Advanced Industrial Science and Technology, Tokyo, Japan.
  • Kaji H; Division of Structural and Synthetic Biology, RIKEN Center for Life Science Technologies, Yokohama, Japan.
PLoS One ; 12(5): e0177972, 2017.
Article em En | MEDLINE | ID: mdl-28542628
ABSTRACT
A model Post-Termination Complex (PoTC) used for the discovery of Ribosome Recycling Factor (RRF) was purified and characterized by cryo-electron microscopic analysis and biochemical methods. We established that the model PoTC has mostly one tRNA, at the P/E or P/P position, together with one mRNA. The structural studies were supported by the biochemical measurement of bound tRNA and mRNA. Using this substrate, we establish that the release of tRNA, release of mRNA and splitting of ribosomal subunits occur during the recycling reaction. Order of these events is tRNA release first followed by mRNA release and splitting almost simultaneously. Moreover, we demonstrate that IF3 is not involved in any of the recycling reactions but simply prevents the re-association of split ribosomal subunits. Our finding demonstrates that the important function of RRF includes the release of mRNA, which is often missed by the use of a short ORF with the Shine-Dalgarno sequence near the termination site.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Terminação Traducional da Cadeia Peptídica / Proteínas Ribossômicas / Ribossomos / Fatores de Terminação de Peptídeos / Fator G para Elongação de Peptídeos / Escherichia coli Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Terminação Traducional da Cadeia Peptídica / Proteínas Ribossômicas / Ribossomos / Fatores de Terminação de Peptídeos / Fator G para Elongação de Peptídeos / Escherichia coli Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2017 Tipo de documento: Article