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Connectivity in gene coexpression networks negatively correlates with rates of molecular evolution in flowering plants
Gene coexpression networks are a useful tool for summarizing transcriptomic data and providing insight into patterns of gene regulation in a variety of species. Though there has been considerable interest in studying the evolution of network topology across species, less attention has been paid to t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536297/ https://www.ncbi.nlm.nih.gov/pubmed/28759647 http://dx.doi.org/10.1371/journal.pone.0182289 |
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author | Masalia, Rishi R. Bewick, Adam J. Burke, John M. |
author_facet | Masalia, Rishi R. Bewick, Adam J. Burke, John M. |
author_sort | Masalia, Rishi R. |
collection | PubMed |
description | Gene coexpression networks are a useful tool for summarizing transcriptomic data and providing insight into patterns of gene regulation in a variety of species. Though there has been considerable interest in studying the evolution of network topology across species, less attention has been paid to the relationship between network position and patterns of molecular evolution. Here, we generated coexpression networks from publicly available expression data for seven flowering plant taxa (Arabidopsis thaliana, Glycine max, Oryza sativa, Populus spp., Solanum lycopersicum, Vitis spp., and Zea mays) to investigate the relationship between network position and rates of molecular evolution. We found a significant negative correlation between network connectivity and rates of molecular evolution, with more highly connected (i.e., “hub”) genes having significantly lower nonsynonymous substitution rates and dN/dS ratios compared to less highly connected (i.e., “peripheral”) genes across the taxa surveyed. These findings suggest that more centrally located hub genes are, on average, subject to higher levels of evolutionary constraint than are genes located on the periphery of gene coexpression networks. The consistency of this result across disparate taxa suggests that it holds for flowering plants in general, as opposed to being a species-specific phenomenon. |
format | Online Article Text |
id | pubmed-5536297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55362972017-08-07 Connectivity in gene coexpression networks negatively correlates with rates of molecular evolution in flowering plants Masalia, Rishi R. Bewick, Adam J. Burke, John M. PLoS One Research Article Gene coexpression networks are a useful tool for summarizing transcriptomic data and providing insight into patterns of gene regulation in a variety of species. Though there has been considerable interest in studying the evolution of network topology across species, less attention has been paid to the relationship between network position and patterns of molecular evolution. Here, we generated coexpression networks from publicly available expression data for seven flowering plant taxa (Arabidopsis thaliana, Glycine max, Oryza sativa, Populus spp., Solanum lycopersicum, Vitis spp., and Zea mays) to investigate the relationship between network position and rates of molecular evolution. We found a significant negative correlation between network connectivity and rates of molecular evolution, with more highly connected (i.e., “hub”) genes having significantly lower nonsynonymous substitution rates and dN/dS ratios compared to less highly connected (i.e., “peripheral”) genes across the taxa surveyed. These findings suggest that more centrally located hub genes are, on average, subject to higher levels of evolutionary constraint than are genes located on the periphery of gene coexpression networks. The consistency of this result across disparate taxa suggests that it holds for flowering plants in general, as opposed to being a species-specific phenomenon. Public Library of Science 2017-07-31 /pmc/articles/PMC5536297/ /pubmed/28759647 http://dx.doi.org/10.1371/journal.pone.0182289 Text en © 2017 Masalia et al 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 author and source are credited. |
spellingShingle | Research Article Masalia, Rishi R. Bewick, Adam J. Burke, John M. Connectivity in gene coexpression networks negatively correlates with rates of molecular evolution in flowering plants |
title | Connectivity in gene coexpression networks negatively correlates with rates of molecular evolution in flowering plants |
title_full | Connectivity in gene coexpression networks negatively correlates with rates of molecular evolution in flowering plants |
title_fullStr | Connectivity in gene coexpression networks negatively correlates with rates of molecular evolution in flowering plants |
title_full_unstemmed | Connectivity in gene coexpression networks negatively correlates with rates of molecular evolution in flowering plants |
title_short | Connectivity in gene coexpression networks negatively correlates with rates of molecular evolution in flowering plants |
title_sort | connectivity in gene coexpression networks negatively correlates with rates of molecular evolution in flowering plants |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5536297/ https://www.ncbi.nlm.nih.gov/pubmed/28759647 http://dx.doi.org/10.1371/journal.pone.0182289 |
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