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Dietary nitrogen alters codon bias and genome composition in parasitic microorganisms
BACKGROUND: Genomes are composed of long strings of nucleotide monomers (A, C, G and T) that are either scavenged from the organism’s environment or built from metabolic precursors. The biosynthesis of each nucleotide differs in atomic requirements with different nucleotides requiring different quan...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5109750/ https://www.ncbi.nlm.nih.gov/pubmed/27842572 http://dx.doi.org/10.1186/s13059-016-1087-9 |
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author | Seward, Emily A. Kelly, Steven |
author_facet | Seward, Emily A. Kelly, Steven |
author_sort | Seward, Emily A. |
collection | PubMed |
description | BACKGROUND: Genomes are composed of long strings of nucleotide monomers (A, C, G and T) that are either scavenged from the organism’s environment or built from metabolic precursors. The biosynthesis of each nucleotide differs in atomic requirements with different nucleotides requiring different quantities of nitrogen atoms. However, the impact of the relative availability of dietary nitrogen on genome composition and codon bias is poorly understood. RESULTS: Here we show that differential nitrogen availability, due to differences in environment and dietary inputs, is a major determinant of genome nucleotide composition and synonymous codon use in both bacterial and eukaryotic microorganisms. Specifically, low nitrogen availability species use nucleotides that require fewer nitrogen atoms to encode the same genes compared to high nitrogen availability species. Furthermore, we provide a novel selection-mutation framework for the evaluation of the impact of metabolism on gene sequence evolution and show that it is possible to predict the metabolic inputs of related organisms from an analysis of the raw nucleotide sequence of their genes. CONCLUSIONS: Taken together, these results reveal a previously hidden relationship between cellular metabolism and genome evolution and provide new insight into how genome sequence evolution can be influenced by adaptation to different diets and environments. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-016-1087-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5109750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-51097502016-11-25 Dietary nitrogen alters codon bias and genome composition in parasitic microorganisms Seward, Emily A. Kelly, Steven Genome Biol Research BACKGROUND: Genomes are composed of long strings of nucleotide monomers (A, C, G and T) that are either scavenged from the organism’s environment or built from metabolic precursors. The biosynthesis of each nucleotide differs in atomic requirements with different nucleotides requiring different quantities of nitrogen atoms. However, the impact of the relative availability of dietary nitrogen on genome composition and codon bias is poorly understood. RESULTS: Here we show that differential nitrogen availability, due to differences in environment and dietary inputs, is a major determinant of genome nucleotide composition and synonymous codon use in both bacterial and eukaryotic microorganisms. Specifically, low nitrogen availability species use nucleotides that require fewer nitrogen atoms to encode the same genes compared to high nitrogen availability species. Furthermore, we provide a novel selection-mutation framework for the evaluation of the impact of metabolism on gene sequence evolution and show that it is possible to predict the metabolic inputs of related organisms from an analysis of the raw nucleotide sequence of their genes. CONCLUSIONS: Taken together, these results reveal a previously hidden relationship between cellular metabolism and genome evolution and provide new insight into how genome sequence evolution can be influenced by adaptation to different diets and environments. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-016-1087-9) contains supplementary material, which is available to authorized users. BioMed Central 2016-11-15 /pmc/articles/PMC5109750/ /pubmed/27842572 http://dx.doi.org/10.1186/s13059-016-1087-9 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Seward, Emily A. Kelly, Steven Dietary nitrogen alters codon bias and genome composition in parasitic microorganisms |
title | Dietary nitrogen alters codon bias and genome composition in parasitic microorganisms |
title_full | Dietary nitrogen alters codon bias and genome composition in parasitic microorganisms |
title_fullStr | Dietary nitrogen alters codon bias and genome composition in parasitic microorganisms |
title_full_unstemmed | Dietary nitrogen alters codon bias and genome composition in parasitic microorganisms |
title_short | Dietary nitrogen alters codon bias and genome composition in parasitic microorganisms |
title_sort | dietary nitrogen alters codon bias and genome composition in parasitic microorganisms |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5109750/ https://www.ncbi.nlm.nih.gov/pubmed/27842572 http://dx.doi.org/10.1186/s13059-016-1087-9 |
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