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Translation efficiency in humans: tissue specificity, global optimization and differences between developmental stages
Various studies in unicellular and multicellular organisms have shown that codon bias plays a significant role in translation efficiency (TE) by co-adaptation to the tRNA pool. Yet, in humans and other mammals the role of codon bias is still an open question, with contradictory results from differen...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2875035/ https://www.ncbi.nlm.nih.gov/pubmed/20097653 http://dx.doi.org/10.1093/nar/gkq009 |
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author | Waldman, Yedael Y. Tuller, Tamir Shlomi, Tomer Sharan, Roded Ruppin, Eytan |
author_facet | Waldman, Yedael Y. Tuller, Tamir Shlomi, Tomer Sharan, Roded Ruppin, Eytan |
author_sort | Waldman, Yedael Y. |
collection | PubMed |
description | Various studies in unicellular and multicellular organisms have shown that codon bias plays a significant role in translation efficiency (TE) by co-adaptation to the tRNA pool. Yet, in humans and other mammals the role of codon bias is still an open question, with contradictory results from different studies. Here we address this question, performing a large-scale tissue-specific analysis of TE in humans, using the tRNA Adaptation Index (tAI) as a direct measure for TE. We find tAI to significantly correlate with expression levels both in tissue-specific and in global expression measures, testifying to the TE of human tissues. Interestingly, we find significantly higher correlations in adult tissues as opposed to fetal tissues, suggesting that the tRNA pool is more adjusted to the adult period. Optimization based analysis suggests that the tRNA pool—codon bias co-adaptation is globally (and not tissue-specific) driven. Additionally, we find that tAI correlates with several measures related to the protein functionally importance, including gene essentiality. Using inferred tissue-specific tRNA pools lead to similar results and shows that tissue-specific genes are more adapted to their tRNA pool than other genes and that related sets of functional gene groups are translated efficiently in each tissue. Similar results are obtained for other mammals. Taken together, these results demonstrate the role of codon bias in TE in humans, and pave the way for future studies of tissue-specific TE in multicellular organisms. |
format | Text |
id | pubmed-2875035 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28750352010-05-24 Translation efficiency in humans: tissue specificity, global optimization and differences between developmental stages Waldman, Yedael Y. Tuller, Tamir Shlomi, Tomer Sharan, Roded Ruppin, Eytan Nucleic Acids Res Genomics Various studies in unicellular and multicellular organisms have shown that codon bias plays a significant role in translation efficiency (TE) by co-adaptation to the tRNA pool. Yet, in humans and other mammals the role of codon bias is still an open question, with contradictory results from different studies. Here we address this question, performing a large-scale tissue-specific analysis of TE in humans, using the tRNA Adaptation Index (tAI) as a direct measure for TE. We find tAI to significantly correlate with expression levels both in tissue-specific and in global expression measures, testifying to the TE of human tissues. Interestingly, we find significantly higher correlations in adult tissues as opposed to fetal tissues, suggesting that the tRNA pool is more adjusted to the adult period. Optimization based analysis suggests that the tRNA pool—codon bias co-adaptation is globally (and not tissue-specific) driven. Additionally, we find that tAI correlates with several measures related to the protein functionally importance, including gene essentiality. Using inferred tissue-specific tRNA pools lead to similar results and shows that tissue-specific genes are more adapted to their tRNA pool than other genes and that related sets of functional gene groups are translated efficiently in each tissue. Similar results are obtained for other mammals. Taken together, these results demonstrate the role of codon bias in TE in humans, and pave the way for future studies of tissue-specific TE in multicellular organisms. Oxford University Press 2010-05 2010-01-21 /pmc/articles/PMC2875035/ /pubmed/20097653 http://dx.doi.org/10.1093/nar/gkq009 Text en © The Author(s) 2010. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Genomics Waldman, Yedael Y. Tuller, Tamir Shlomi, Tomer Sharan, Roded Ruppin, Eytan Translation efficiency in humans: tissue specificity, global optimization and differences between developmental stages |
title | Translation efficiency in humans: tissue specificity, global optimization and differences between developmental stages |
title_full | Translation efficiency in humans: tissue specificity, global optimization and differences between developmental stages |
title_fullStr | Translation efficiency in humans: tissue specificity, global optimization and differences between developmental stages |
title_full_unstemmed | Translation efficiency in humans: tissue specificity, global optimization and differences between developmental stages |
title_short | Translation efficiency in humans: tissue specificity, global optimization and differences between developmental stages |
title_sort | translation efficiency in humans: tissue specificity, global optimization and differences between developmental stages |
topic | Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2875035/ https://www.ncbi.nlm.nih.gov/pubmed/20097653 http://dx.doi.org/10.1093/nar/gkq009 |
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