Cargando…
Structural basis for the transition from translation initiation to elongation by an 80S-eIF5B complex
Recognition of a start codon by the initiator aminoacyl-tRNA determines the reading frame of messenger RNA (mRNA) translation by the ribosome. In eukaryotes, the GTPase eIF5B collaborates in the correct positioning of the initiator Met-tRNA(i)(Met) on the ribosome in the later stages of translation...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7538418/ https://www.ncbi.nlm.nih.gov/pubmed/33024099 http://dx.doi.org/10.1038/s41467-020-18829-3 |
_version_ | 1783590865915084800 |
---|---|
author | Wang, Jinfan Wang, Jing Shin, Byung-Sik Kim, Joo-Ran Dever, Thomas E. Puglisi, Joseph D. Fernández, Israel S. |
author_facet | Wang, Jinfan Wang, Jing Shin, Byung-Sik Kim, Joo-Ran Dever, Thomas E. Puglisi, Joseph D. Fernández, Israel S. |
author_sort | Wang, Jinfan |
collection | PubMed |
description | Recognition of a start codon by the initiator aminoacyl-tRNA determines the reading frame of messenger RNA (mRNA) translation by the ribosome. In eukaryotes, the GTPase eIF5B collaborates in the correct positioning of the initiator Met-tRNA(i)(Met) on the ribosome in the later stages of translation initiation, gating entrance into elongation. Leveraging the long residence time of eIF5B on the ribosome recently identified by single-molecule fluorescence measurements, we determine the cryoEM structure of the naturally long-lived ribosome complex with eIF5B and Met-tRNA(i)(Met) immediately before transition into elongation. The structure uncovers an unexpected, eukaryotic specific and dynamic fidelity checkpoint implemented by eIF5B in concert with components of the large ribosomal subunit. |
format | Online Article Text |
id | pubmed-7538418 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75384182020-10-19 Structural basis for the transition from translation initiation to elongation by an 80S-eIF5B complex Wang, Jinfan Wang, Jing Shin, Byung-Sik Kim, Joo-Ran Dever, Thomas E. Puglisi, Joseph D. Fernández, Israel S. Nat Commun Article Recognition of a start codon by the initiator aminoacyl-tRNA determines the reading frame of messenger RNA (mRNA) translation by the ribosome. In eukaryotes, the GTPase eIF5B collaborates in the correct positioning of the initiator Met-tRNA(i)(Met) on the ribosome in the later stages of translation initiation, gating entrance into elongation. Leveraging the long residence time of eIF5B on the ribosome recently identified by single-molecule fluorescence measurements, we determine the cryoEM structure of the naturally long-lived ribosome complex with eIF5B and Met-tRNA(i)(Met) immediately before transition into elongation. The structure uncovers an unexpected, eukaryotic specific and dynamic fidelity checkpoint implemented by eIF5B in concert with components of the large ribosomal subunit. Nature Publishing Group UK 2020-10-06 /pmc/articles/PMC7538418/ /pubmed/33024099 http://dx.doi.org/10.1038/s41467-020-18829-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wang, Jinfan Wang, Jing Shin, Byung-Sik Kim, Joo-Ran Dever, Thomas E. Puglisi, Joseph D. Fernández, Israel S. Structural basis for the transition from translation initiation to elongation by an 80S-eIF5B complex |
title | Structural basis for the transition from translation initiation to elongation by an 80S-eIF5B complex |
title_full | Structural basis for the transition from translation initiation to elongation by an 80S-eIF5B complex |
title_fullStr | Structural basis for the transition from translation initiation to elongation by an 80S-eIF5B complex |
title_full_unstemmed | Structural basis for the transition from translation initiation to elongation by an 80S-eIF5B complex |
title_short | Structural basis for the transition from translation initiation to elongation by an 80S-eIF5B complex |
title_sort | structural basis for the transition from translation initiation to elongation by an 80s-eif5b complex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7538418/ https://www.ncbi.nlm.nih.gov/pubmed/33024099 http://dx.doi.org/10.1038/s41467-020-18829-3 |
work_keys_str_mv | AT wangjinfan structuralbasisforthetransitionfromtranslationinitiationtoelongationbyan80seif5bcomplex AT wangjing structuralbasisforthetransitionfromtranslationinitiationtoelongationbyan80seif5bcomplex AT shinbyungsik structuralbasisforthetransitionfromtranslationinitiationtoelongationbyan80seif5bcomplex AT kimjooran structuralbasisforthetransitionfromtranslationinitiationtoelongationbyan80seif5bcomplex AT deverthomase structuralbasisforthetransitionfromtranslationinitiationtoelongationbyan80seif5bcomplex AT puglisijosephd structuralbasisforthetransitionfromtranslationinitiationtoelongationbyan80seif5bcomplex AT fernandezisraels structuralbasisforthetransitionfromtranslationinitiationtoelongationbyan80seif5bcomplex |