cris.boxmetadata.label.title
Role of the initiation factors in mRNA start site selection and fMet-tRNA recruitment by bacterial ribosomes
cris.boxmetadata.label.dateissued
18 browse.startsWith.months.june 2010
cris.boxmetadata.label.accesslevel
open access
cris.boxmetadata.label.resourcetype
review
cris.boxmetadata.label.authors
Gualerzi C.
Fabbretti A.
Brandi L.
MILON MAYER, POHL LUIS
Pon C.
University of Camerino
cris.boxmetadata.label.abstract
Translation initiation is a complex, multi-step process of fundamental importance in all kingdoms of life, during which the start site of the genetic message transmitted in the form of an RNA molecule (mRNA) is selected, and the level of translation determined. Being the slowest step of protein synthesis, initiation is the phase most often subject to regulation. Here we review, in a historical perspective and focusing mainly on results from our laboratory, the development of our perception of the mechanisms by which the most relevant steps of this pathway occur in bacteria. In particular, we describe: (a) the mechanistics and kinetics of translation initiation; (b) properties of mRNAs with and without Shine-Dalgarno sequence relevant for initiation site selection and translational efficiency; c) ribosomal binding and dissociation of the initiation factors, formation and properties of translation initiation intermediates; (d) the mechanisms by which translation initiation fidelity is ensured. Finally, we provide a short survey of the known translation initiation inhibitors. Copyright © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
cris.boxmetadata.label.citationstartpage
80
cris.boxmetadata.label.citationendpage
94
cris.boxmetadata.label.volume
50
cris.boxmetadata.label.issue
1
cris.boxmetadata.label.language
English
cris.boxmetadata.label.ocdeknowledgeArea
Biología celular, Microbiología
cris.boxmetadata.label.doi
cris.boxmetadata.label.scopusidentifier
2-s2.0-78649508041
cris.boxmetadata.label.source
Israel Journal of Chemistry
cris.boxmetadata.label.containerissn
18695868
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