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Ribosome profiling reveals pervasive and regulated stop codon readthrough in Drosophila melanogaster
Ribosomes can read through stop codons in a regulated manner, elongating rather than terminating the nascent peptide. Stop codon readthrough is essential to diverse viruses, and phylogenetically predicted to occur in a few hundred genes in Drosophila melanogaster, but the importance of regulated rea...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840789/ https://www.ncbi.nlm.nih.gov/pubmed/24302569 http://dx.doi.org/10.7554/eLife.01179 |
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author | Dunn, Joshua G Foo, Catherine K Belletier, Nicolette G Gavis, Elizabeth R Weissman, Jonathan S |
author_facet | Dunn, Joshua G Foo, Catherine K Belletier, Nicolette G Gavis, Elizabeth R Weissman, Jonathan S |
author_sort | Dunn, Joshua G |
collection | PubMed |
description | Ribosomes can read through stop codons in a regulated manner, elongating rather than terminating the nascent peptide. Stop codon readthrough is essential to diverse viruses, and phylogenetically predicted to occur in a few hundred genes in Drosophila melanogaster, but the importance of regulated readthrough in eukaryotes remains largely unexplored. Here, we present a ribosome profiling assay (deep sequencing of ribosome-protected mRNA fragments) for Drosophila melanogaster, and provide the first genome-wide experimental analysis of readthrough. Readthrough is far more pervasive than expected: the vast majority of readthrough events evolved within D. melanogaster and were not predicted phylogenetically. The resulting C-terminal protein extensions show evidence of selection, contain functional subcellular localization signals, and their readthrough is regulated, arguing for their importance. We further demonstrate that readthrough occurs in yeast and humans. Readthrough thus provides general mechanisms both to regulate gene expression and function, and to add plasticity to the proteome during evolution. DOI: http://dx.doi.org/10.7554/eLife.01179.001 |
format | Online Article Text |
id | pubmed-3840789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-38407892013-12-04 Ribosome profiling reveals pervasive and regulated stop codon readthrough in Drosophila melanogaster Dunn, Joshua G Foo, Catherine K Belletier, Nicolette G Gavis, Elizabeth R Weissman, Jonathan S eLife Cell Biology Ribosomes can read through stop codons in a regulated manner, elongating rather than terminating the nascent peptide. Stop codon readthrough is essential to diverse viruses, and phylogenetically predicted to occur in a few hundred genes in Drosophila melanogaster, but the importance of regulated readthrough in eukaryotes remains largely unexplored. Here, we present a ribosome profiling assay (deep sequencing of ribosome-protected mRNA fragments) for Drosophila melanogaster, and provide the first genome-wide experimental analysis of readthrough. Readthrough is far more pervasive than expected: the vast majority of readthrough events evolved within D. melanogaster and were not predicted phylogenetically. The resulting C-terminal protein extensions show evidence of selection, contain functional subcellular localization signals, and their readthrough is regulated, arguing for their importance. We further demonstrate that readthrough occurs in yeast and humans. Readthrough thus provides general mechanisms both to regulate gene expression and function, and to add plasticity to the proteome during evolution. DOI: http://dx.doi.org/10.7554/eLife.01179.001 eLife Sciences Publications, Ltd 2013-12-03 /pmc/articles/PMC3840789/ /pubmed/24302569 http://dx.doi.org/10.7554/eLife.01179 Text en Copyright © 2013, Dunn et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Dunn, Joshua G Foo, Catherine K Belletier, Nicolette G Gavis, Elizabeth R Weissman, Jonathan S Ribosome profiling reveals pervasive and regulated stop codon readthrough in Drosophila melanogaster |
title | Ribosome profiling reveals pervasive and regulated stop codon readthrough in Drosophila melanogaster |
title_full | Ribosome profiling reveals pervasive and regulated stop codon readthrough in Drosophila melanogaster |
title_fullStr | Ribosome profiling reveals pervasive and regulated stop codon readthrough in Drosophila melanogaster |
title_full_unstemmed | Ribosome profiling reveals pervasive and regulated stop codon readthrough in Drosophila melanogaster |
title_short | Ribosome profiling reveals pervasive and regulated stop codon readthrough in Drosophila melanogaster |
title_sort | ribosome profiling reveals pervasive and regulated stop codon readthrough in drosophila melanogaster |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840789/ https://www.ncbi.nlm.nih.gov/pubmed/24302569 http://dx.doi.org/10.7554/eLife.01179 |
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