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Properties and determinants of codon decoding time distributions
BACKGROUND: Codon decoding time is a fundamental property of mRNA translation believed to affect the abundance, function, and properties of proteins. Recently, a novel experimental technology--ribosome profiling--was developed to measure the density, and thus the speed, of ribosomes at codon resolut...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4240079/ https://www.ncbi.nlm.nih.gov/pubmed/25572668 http://dx.doi.org/10.1186/1471-2164-15-S6-S13 |
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author | Dana, Alexandra Tuller, Tamir |
author_facet | Dana, Alexandra Tuller, Tamir |
author_sort | Dana, Alexandra |
collection | PubMed |
description | BACKGROUND: Codon decoding time is a fundamental property of mRNA translation believed to affect the abundance, function, and properties of proteins. Recently, a novel experimental technology--ribosome profiling--was developed to measure the density, and thus the speed, of ribosomes at codon resolution. Specifically, this method is based on next-generation sequencing, which theoretically can provide footprint counts that correspond to the probability of observing a ribosome in this position for each nucleotide in each transcript. RESULTS: In this study, we report for the first time various novel properties of the distribution of codon footprint counts in five organisms, based on large-scale analysis of ribosomal profiling data. We show that codons have distinctive footprint count distributions. These tend to be preserved along the inner part of the ORF, but differ at the 5' and 3' ends of the ORF, suggesting that the translation-elongation stage actually includes three biophysical sub-steps. In addition, we study various basic properties of the codon footprint count distributions and show that some of them correlate with the abundance of the tRNA molecule types recognizing them. CONCLUSIONS: Our approach emphasizes the advantages of analyzing ribosome profiling and similar types of data via a comparative genomic codon-distribution-centric view. Thus, our methods can be used in future studies related to translation and even transcription elongation. |
format | Online Article Text |
id | pubmed-4240079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42400792014-11-25 Properties and determinants of codon decoding time distributions Dana, Alexandra Tuller, Tamir BMC Genomics Research BACKGROUND: Codon decoding time is a fundamental property of mRNA translation believed to affect the abundance, function, and properties of proteins. Recently, a novel experimental technology--ribosome profiling--was developed to measure the density, and thus the speed, of ribosomes at codon resolution. Specifically, this method is based on next-generation sequencing, which theoretically can provide footprint counts that correspond to the probability of observing a ribosome in this position for each nucleotide in each transcript. RESULTS: In this study, we report for the first time various novel properties of the distribution of codon footprint counts in five organisms, based on large-scale analysis of ribosomal profiling data. We show that codons have distinctive footprint count distributions. These tend to be preserved along the inner part of the ORF, but differ at the 5' and 3' ends of the ORF, suggesting that the translation-elongation stage actually includes three biophysical sub-steps. In addition, we study various basic properties of the codon footprint count distributions and show that some of them correlate with the abundance of the tRNA molecule types recognizing them. CONCLUSIONS: Our approach emphasizes the advantages of analyzing ribosome profiling and similar types of data via a comparative genomic codon-distribution-centric view. Thus, our methods can be used in future studies related to translation and even transcription elongation. BioMed Central 2014-10-17 /pmc/articles/PMC4240079/ /pubmed/25572668 http://dx.doi.org/10.1186/1471-2164-15-S6-S13 Text en Copyright © 2014 Dana and Tuller; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Dana, Alexandra Tuller, Tamir Properties and determinants of codon decoding time distributions |
title | Properties and determinants of codon decoding time distributions |
title_full | Properties and determinants of codon decoding time distributions |
title_fullStr | Properties and determinants of codon decoding time distributions |
title_full_unstemmed | Properties and determinants of codon decoding time distributions |
title_short | Properties and determinants of codon decoding time distributions |
title_sort | properties and determinants of codon decoding time distributions |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4240079/ https://www.ncbi.nlm.nih.gov/pubmed/25572668 http://dx.doi.org/10.1186/1471-2164-15-S6-S13 |
work_keys_str_mv | AT danaalexandra propertiesanddeterminantsofcodondecodingtimedistributions AT tullertamir propertiesanddeterminantsofcodondecodingtimedistributions |