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Position dependent termination and widespread obligatory frameshifting in Euplotes translation
The ribosome can change its reading frame during translation in a process known as programmed ribosomal frameshifting. These rare events are supported by complex mRNA signals. However, we found that the ciliates Euplotes crassus and Euplotes focardii exhibit widespread frameshifting at stop codons....
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295771/ https://www.ncbi.nlm.nih.gov/pubmed/27870834 http://dx.doi.org/10.1038/nsmb.3330 |
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author | Lobanov, Alexei V. Heaphy, Stephen M. Turanov, Anton A. Gerashchenko, Maxim V. Pucciarelli, Sandra Devaraj, Raghul R. Xie, Fang Petyuk, Vladislav A. Smith, Richard D. Klobutcher, Lawrence A. Atkins, John F. Miceli, Cristina Hatfield, Dolph L. Baranov, Pavel V. Gladyshev, Vadim N. |
author_facet | Lobanov, Alexei V. Heaphy, Stephen M. Turanov, Anton A. Gerashchenko, Maxim V. Pucciarelli, Sandra Devaraj, Raghul R. Xie, Fang Petyuk, Vladislav A. Smith, Richard D. Klobutcher, Lawrence A. Atkins, John F. Miceli, Cristina Hatfield, Dolph L. Baranov, Pavel V. Gladyshev, Vadim N. |
author_sort | Lobanov, Alexei V. |
collection | PubMed |
description | The ribosome can change its reading frame during translation in a process known as programmed ribosomal frameshifting. These rare events are supported by complex mRNA signals. However, we found that the ciliates Euplotes crassus and Euplotes focardii exhibit widespread frameshifting at stop codons. 47 different codons preceding stop signals resulted in either +1 or +2 frameshifts, with the +1 frameshifting at AAA being the most frequent. The frameshifts show unusual plasticity and rapid evolution, and have little influence on translation rates. Proximity of a stop codon to the 3′-mRNA end rather than its occurrence or sequence context appeared to designate termination. Thus, a stop codon is not a sufficient signal for translation termination, and the default function of stop codons in Euplotes is frameshifting, whereas termination is specific to certain mRNA positions and likely requires additional factors. |
format | Online Article Text |
id | pubmed-5295771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
record_format | MEDLINE/PubMed |
spelling | pubmed-52957712017-05-21 Position dependent termination and widespread obligatory frameshifting in Euplotes translation Lobanov, Alexei V. Heaphy, Stephen M. Turanov, Anton A. Gerashchenko, Maxim V. Pucciarelli, Sandra Devaraj, Raghul R. Xie, Fang Petyuk, Vladislav A. Smith, Richard D. Klobutcher, Lawrence A. Atkins, John F. Miceli, Cristina Hatfield, Dolph L. Baranov, Pavel V. Gladyshev, Vadim N. Nat Struct Mol Biol Article The ribosome can change its reading frame during translation in a process known as programmed ribosomal frameshifting. These rare events are supported by complex mRNA signals. However, we found that the ciliates Euplotes crassus and Euplotes focardii exhibit widespread frameshifting at stop codons. 47 different codons preceding stop signals resulted in either +1 or +2 frameshifts, with the +1 frameshifting at AAA being the most frequent. The frameshifts show unusual plasticity and rapid evolution, and have little influence on translation rates. Proximity of a stop codon to the 3′-mRNA end rather than its occurrence or sequence context appeared to designate termination. Thus, a stop codon is not a sufficient signal for translation termination, and the default function of stop codons in Euplotes is frameshifting, whereas termination is specific to certain mRNA positions and likely requires additional factors. 2016-11-21 2017-01 /pmc/articles/PMC5295771/ /pubmed/27870834 http://dx.doi.org/10.1038/nsmb.3330 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Lobanov, Alexei V. Heaphy, Stephen M. Turanov, Anton A. Gerashchenko, Maxim V. Pucciarelli, Sandra Devaraj, Raghul R. Xie, Fang Petyuk, Vladislav A. Smith, Richard D. Klobutcher, Lawrence A. Atkins, John F. Miceli, Cristina Hatfield, Dolph L. Baranov, Pavel V. Gladyshev, Vadim N. Position dependent termination and widespread obligatory frameshifting in Euplotes translation |
title | Position dependent termination and widespread obligatory frameshifting in Euplotes translation |
title_full | Position dependent termination and widespread obligatory frameshifting in Euplotes translation |
title_fullStr | Position dependent termination and widespread obligatory frameshifting in Euplotes translation |
title_full_unstemmed | Position dependent termination and widespread obligatory frameshifting in Euplotes translation |
title_short | Position dependent termination and widespread obligatory frameshifting in Euplotes translation |
title_sort | position dependent termination and widespread obligatory frameshifting in euplotes translation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295771/ https://www.ncbi.nlm.nih.gov/pubmed/27870834 http://dx.doi.org/10.1038/nsmb.3330 |
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