Cargando…

Structure of a 30S pre-initiation complex stalled by GE81112 reveals structural parallels in bacterial and eukaryotic protein synthesis initiation pathways

In bacteria, the start site and the reading frame of the messenger RNA are selected by the small ribosomal subunit (30S) when the start codon, typically an AUG, is decoded in the P-site by the initiator tRNA in a process guided and controlled by three initiation factors. This process can be efficien...

Descripción completa

Detalles Bibliográficos
Autores principales: López-Alonso, Jorge P., Fabbretti, Attilio, Kaminishi, Tatsuya, Iturrioz, Idoia, Brandi, Letizia, Gil-Carton, David, Gualerzi, Claudio O., Fucini, Paola, Connell, Sean R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389724/
https://www.ncbi.nlm.nih.gov/pubmed/27986852
http://dx.doi.org/10.1093/nar/gkw1251
_version_ 1782521329018208256
author López-Alonso, Jorge P.
Fabbretti, Attilio
Kaminishi, Tatsuya
Iturrioz, Idoia
Brandi, Letizia
Gil-Carton, David
Gualerzi, Claudio O.
Fucini, Paola
Connell, Sean R.
author_facet López-Alonso, Jorge P.
Fabbretti, Attilio
Kaminishi, Tatsuya
Iturrioz, Idoia
Brandi, Letizia
Gil-Carton, David
Gualerzi, Claudio O.
Fucini, Paola
Connell, Sean R.
author_sort López-Alonso, Jorge P.
collection PubMed
description In bacteria, the start site and the reading frame of the messenger RNA are selected by the small ribosomal subunit (30S) when the start codon, typically an AUG, is decoded in the P-site by the initiator tRNA in a process guided and controlled by three initiation factors. This process can be efficiently inhibited by GE81112, a natural tetrapeptide antibiotic that is highly specific toward bacteria. Here GE81112 was used to stabilize the 30S pre-initiation complex and obtain its structure by cryo-electron microscopy. The results obtained reveal the occurrence of changes in both the ribosome conformation and initiator tRNA position that may play a critical role in controlling translational fidelity. Furthermore, the structure highlights similarities with the early steps of initiation in eukaryotes suggesting that shared structural features guide initiation in all kingdoms of life.
format Online
Article
Text
id pubmed-5389724
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-53897242017-04-24 Structure of a 30S pre-initiation complex stalled by GE81112 reveals structural parallels in bacterial and eukaryotic protein synthesis initiation pathways López-Alonso, Jorge P. Fabbretti, Attilio Kaminishi, Tatsuya Iturrioz, Idoia Brandi, Letizia Gil-Carton, David Gualerzi, Claudio O. Fucini, Paola Connell, Sean R. Nucleic Acids Res Structural Biology In bacteria, the start site and the reading frame of the messenger RNA are selected by the small ribosomal subunit (30S) when the start codon, typically an AUG, is decoded in the P-site by the initiator tRNA in a process guided and controlled by three initiation factors. This process can be efficiently inhibited by GE81112, a natural tetrapeptide antibiotic that is highly specific toward bacteria. Here GE81112 was used to stabilize the 30S pre-initiation complex and obtain its structure by cryo-electron microscopy. The results obtained reveal the occurrence of changes in both the ribosome conformation and initiator tRNA position that may play a critical role in controlling translational fidelity. Furthermore, the structure highlights similarities with the early steps of initiation in eukaryotes suggesting that shared structural features guide initiation in all kingdoms of life. Oxford University Press 2017-02-28 2016-12-16 /pmc/articles/PMC5389724/ /pubmed/27986852 http://dx.doi.org/10.1093/nar/gkw1251 Text en © The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Structural Biology
López-Alonso, Jorge P.
Fabbretti, Attilio
Kaminishi, Tatsuya
Iturrioz, Idoia
Brandi, Letizia
Gil-Carton, David
Gualerzi, Claudio O.
Fucini, Paola
Connell, Sean R.
Structure of a 30S pre-initiation complex stalled by GE81112 reveals structural parallels in bacterial and eukaryotic protein synthesis initiation pathways
title Structure of a 30S pre-initiation complex stalled by GE81112 reveals structural parallels in bacterial and eukaryotic protein synthesis initiation pathways
title_full Structure of a 30S pre-initiation complex stalled by GE81112 reveals structural parallels in bacterial and eukaryotic protein synthesis initiation pathways
title_fullStr Structure of a 30S pre-initiation complex stalled by GE81112 reveals structural parallels in bacterial and eukaryotic protein synthesis initiation pathways
title_full_unstemmed Structure of a 30S pre-initiation complex stalled by GE81112 reveals structural parallels in bacterial and eukaryotic protein synthesis initiation pathways
title_short Structure of a 30S pre-initiation complex stalled by GE81112 reveals structural parallels in bacterial and eukaryotic protein synthesis initiation pathways
title_sort structure of a 30s pre-initiation complex stalled by ge81112 reveals structural parallels in bacterial and eukaryotic protein synthesis initiation pathways
topic Structural Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389724/
https://www.ncbi.nlm.nih.gov/pubmed/27986852
http://dx.doi.org/10.1093/nar/gkw1251
work_keys_str_mv AT lopezalonsojorgep structureofa30spreinitiationcomplexstalledbyge81112revealsstructuralparallelsinbacterialandeukaryoticproteinsynthesisinitiationpathways
AT fabbrettiattilio structureofa30spreinitiationcomplexstalledbyge81112revealsstructuralparallelsinbacterialandeukaryoticproteinsynthesisinitiationpathways
AT kaminishitatsuya structureofa30spreinitiationcomplexstalledbyge81112revealsstructuralparallelsinbacterialandeukaryoticproteinsynthesisinitiationpathways
AT iturriozidoia structureofa30spreinitiationcomplexstalledbyge81112revealsstructuralparallelsinbacterialandeukaryoticproteinsynthesisinitiationpathways
AT brandiletizia structureofa30spreinitiationcomplexstalledbyge81112revealsstructuralparallelsinbacterialandeukaryoticproteinsynthesisinitiationpathways
AT gilcartondavid structureofa30spreinitiationcomplexstalledbyge81112revealsstructuralparallelsinbacterialandeukaryoticproteinsynthesisinitiationpathways
AT gualerziclaudioo structureofa30spreinitiationcomplexstalledbyge81112revealsstructuralparallelsinbacterialandeukaryoticproteinsynthesisinitiationpathways
AT fucinipaola structureofa30spreinitiationcomplexstalledbyge81112revealsstructuralparallelsinbacterialandeukaryoticproteinsynthesisinitiationpathways
AT connellseanr structureofa30spreinitiationcomplexstalledbyge81112revealsstructuralparallelsinbacterialandeukaryoticproteinsynthesisinitiationpathways