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Environmental shaping of codon usage and functional adaptation across microbial communities
Microbial communities represent the largest portion of the Earth’s biomass. Metagenomics projects use high-throughput sequencing to survey these communities and shed light on genetic capabilities that enable microbes to inhabit every corner of the biosphere. Metagenome studies are generally based on...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3799439/ https://www.ncbi.nlm.nih.gov/pubmed/23921637 http://dx.doi.org/10.1093/nar/gkt673 |
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author | Roller, Maša Lucić, Vedran Nagy, István Perica, Tina Vlahoviček, Kristian |
author_facet | Roller, Maša Lucić, Vedran Nagy, István Perica, Tina Vlahoviček, Kristian |
author_sort | Roller, Maša |
collection | PubMed |
description | Microbial communities represent the largest portion of the Earth’s biomass. Metagenomics projects use high-throughput sequencing to survey these communities and shed light on genetic capabilities that enable microbes to inhabit every corner of the biosphere. Metagenome studies are generally based on (i) classifying and ranking functions of identified genes; and (ii) estimating the phyletic distribution of constituent microbial species. To understand microbial communities at the systems level, it is necessary to extend these studies beyond the species’ boundaries and capture higher levels of metabolic complexity. We evaluated 11 metagenome samples and demonstrated that microbes inhabiting the same ecological niche share common preferences for synonymous codons, regardless of their phylogeny. By exploring concepts of translational optimization through codon usage adaptation, we demonstrated that community-wide bias in codon usage can be used as a prediction tool for lifestyle-specific genes across the entire microbial community, effectively considering microbial communities as meta-genomes. These findings set up a ‘functional metagenomics’ platform for the identification of genes relevant for adaptations of entire microbial communities to environments. Our results provide valuable arguments in defining the concept of microbial species through the context of their interactions within the community. |
format | Online Article Text |
id | pubmed-3799439 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-37994392013-10-21 Environmental shaping of codon usage and functional adaptation across microbial communities Roller, Maša Lucić, Vedran Nagy, István Perica, Tina Vlahoviček, Kristian Nucleic Acids Res Computational Biology Microbial communities represent the largest portion of the Earth’s biomass. Metagenomics projects use high-throughput sequencing to survey these communities and shed light on genetic capabilities that enable microbes to inhabit every corner of the biosphere. Metagenome studies are generally based on (i) classifying and ranking functions of identified genes; and (ii) estimating the phyletic distribution of constituent microbial species. To understand microbial communities at the systems level, it is necessary to extend these studies beyond the species’ boundaries and capture higher levels of metabolic complexity. We evaluated 11 metagenome samples and demonstrated that microbes inhabiting the same ecological niche share common preferences for synonymous codons, regardless of their phylogeny. By exploring concepts of translational optimization through codon usage adaptation, we demonstrated that community-wide bias in codon usage can be used as a prediction tool for lifestyle-specific genes across the entire microbial community, effectively considering microbial communities as meta-genomes. These findings set up a ‘functional metagenomics’ platform for the identification of genes relevant for adaptations of entire microbial communities to environments. Our results provide valuable arguments in defining the concept of microbial species through the context of their interactions within the community. Oxford University Press 2013-10 2013-08-05 /pmc/articles/PMC3799439/ /pubmed/23921637 http://dx.doi.org/10.1093/nar/gkt673 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Computational Biology Roller, Maša Lucić, Vedran Nagy, István Perica, Tina Vlahoviček, Kristian Environmental shaping of codon usage and functional adaptation across microbial communities |
title | Environmental shaping of codon usage and functional adaptation across microbial communities |
title_full | Environmental shaping of codon usage and functional adaptation across microbial communities |
title_fullStr | Environmental shaping of codon usage and functional adaptation across microbial communities |
title_full_unstemmed | Environmental shaping of codon usage and functional adaptation across microbial communities |
title_short | Environmental shaping of codon usage and functional adaptation across microbial communities |
title_sort | environmental shaping of codon usage and functional adaptation across microbial communities |
topic | Computational Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3799439/ https://www.ncbi.nlm.nih.gov/pubmed/23921637 http://dx.doi.org/10.1093/nar/gkt673 |
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