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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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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 |
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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 |
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