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EF-G–induced ribosome sliding along the noncoding mRNA
Author(s) -
Mariia Klimova,
Tamara Senyushkina,
Ekaterina Samatova,
BeeZen Peng,
Michael Pearson,
Frank Peske,
Marina V. Rodnina
Publication year - 2019
Publication title -
science advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.928
H-Index - 146
ISSN - 2375-2548
DOI - 10.1126/sciadv.aaw9049
Subject(s) - ribosome , translation (biology) , messenger rna , translational frameshift , microbiology and biotechnology , transfer rna , ribosome profiling , rna , biology , ribosomal binding site , protein biosynthesis , shine dalgarno sequence , untranslated region , eukaryotic ribosome , internal ribosome entry site , genetics , gene
Translational bypassing is a recoding event during which ribosomes slide over a noncoding region of the messenger RNA (mRNA) to synthesize one protein from two discontinuous reading frames. Structures in the mRNA orchestrate forward movement of the ribosome, but what causes ribosomes to start sliding remains unclear. Here, we show that elongation factor G (EF-G) triggers ribosome take-off by a pseudotranslocation event using a small mRNA stem-loop as an A-site transfer RNA mimic and requires hydrolysis of about two molecules of guanosine 5'-triphosphate per nucleotide of the noncoding gap. Bypassing ribosomes adopt a hyper-rotated conformation, also observed with ribosomes stalled by the SecM sequence, suggesting common ribosome dynamics during translation stalling. Our results demonstrate a new function of EF-G in promoting ribosome sliding along the mRNA, in contrast to codon-wise ribosome movement during canonical translation, and suggest a mechanism by which ribosomes could traverse untranslated parts of mRNAs.

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