Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Masalia, Rishi R., Bewick, Adam J., Burke, John M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
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
_version_ 1783253994045440000
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
work_keys_str_mv AT masaliarishir connectivityingenecoexpressionnetworksnegativelycorrelateswithratesofmolecularevolutioninfloweringplants
AT bewickadamj connectivityingenecoexpressionnetworksnegativelycorrelateswithratesofmolecularevolutioninfloweringplants
AT burkejohnm connectivityingenecoexpressionnetworksnegativelycorrelateswithratesofmolecularevolutioninfloweringplants