Cargando…

Positive Selection and Centrality in the Yeast and Fly Protein-Protein Interaction Networks

Proteins within a molecular network are expected to be subject to different selective pressures depending on their relative hierarchical positions. However, it is not obvious what genes within a network should be more likely to evolve under positive selection. On one hand, only mutations at genes wi...

Descripción completa

Detalles Bibliográficos
Autores principales: Chakraborty, Sandip, Alvarez-Ponce, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4826914/
https://www.ncbi.nlm.nih.gov/pubmed/27119079
http://dx.doi.org/10.1155/2016/4658506
_version_ 1782426386644860928
author Chakraborty, Sandip
Alvarez-Ponce, David
author_facet Chakraborty, Sandip
Alvarez-Ponce, David
author_sort Chakraborty, Sandip
collection PubMed
description Proteins within a molecular network are expected to be subject to different selective pressures depending on their relative hierarchical positions. However, it is not obvious what genes within a network should be more likely to evolve under positive selection. On one hand, only mutations at genes with a relatively high degree of control over adaptive phenotypes (such as those encoding highly connected proteins) are expected to be “seen” by natural selection. On the other hand, a high degree of pleiotropy at these genes is expected to hinder adaptation. Previous analyses of the human protein-protein interaction network have shown that genes under long-term, recurrent positive selection (as inferred from interspecific comparisons) tend to act at the periphery of the network. It is unknown, however, whether these trends apply to other organisms. Here, we show that long-term positive selection has preferentially targeted the periphery of the yeast interactome. Conversely, in flies, genes under positive selection encode significantly more connected and central proteins. These observations are not due to covariation of genes' adaptability and centrality with confounding factors. Therefore, the distribution of proteins encoded by genes under recurrent positive selection across protein-protein interaction networks varies from one species to another.
format Online
Article
Text
id pubmed-4826914
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-48269142016-04-26 Positive Selection and Centrality in the Yeast and Fly Protein-Protein Interaction Networks Chakraborty, Sandip Alvarez-Ponce, David Biomed Res Int Research Article Proteins within a molecular network are expected to be subject to different selective pressures depending on their relative hierarchical positions. However, it is not obvious what genes within a network should be more likely to evolve under positive selection. On one hand, only mutations at genes with a relatively high degree of control over adaptive phenotypes (such as those encoding highly connected proteins) are expected to be “seen” by natural selection. On the other hand, a high degree of pleiotropy at these genes is expected to hinder adaptation. Previous analyses of the human protein-protein interaction network have shown that genes under long-term, recurrent positive selection (as inferred from interspecific comparisons) tend to act at the periphery of the network. It is unknown, however, whether these trends apply to other organisms. Here, we show that long-term positive selection has preferentially targeted the periphery of the yeast interactome. Conversely, in flies, genes under positive selection encode significantly more connected and central proteins. These observations are not due to covariation of genes' adaptability and centrality with confounding factors. Therefore, the distribution of proteins encoded by genes under recurrent positive selection across protein-protein interaction networks varies from one species to another. Hindawi Publishing Corporation 2016 2016-03-28 /pmc/articles/PMC4826914/ /pubmed/27119079 http://dx.doi.org/10.1155/2016/4658506 Text en Copyright © 2016 S. Chakraborty and D. Alvarez-Ponce. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chakraborty, Sandip
Alvarez-Ponce, David
Positive Selection and Centrality in the Yeast and Fly Protein-Protein Interaction Networks
title Positive Selection and Centrality in the Yeast and Fly Protein-Protein Interaction Networks
title_full Positive Selection and Centrality in the Yeast and Fly Protein-Protein Interaction Networks
title_fullStr Positive Selection and Centrality in the Yeast and Fly Protein-Protein Interaction Networks
title_full_unstemmed Positive Selection and Centrality in the Yeast and Fly Protein-Protein Interaction Networks
title_short Positive Selection and Centrality in the Yeast and Fly Protein-Protein Interaction Networks
title_sort positive selection and centrality in the yeast and fly protein-protein interaction networks
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4826914/
https://www.ncbi.nlm.nih.gov/pubmed/27119079
http://dx.doi.org/10.1155/2016/4658506
work_keys_str_mv AT chakrabortysandip positiveselectionandcentralityintheyeastandflyproteinproteininteractionnetworks
AT alvarezponcedavid positiveselectionandcentralityintheyeastandflyproteinproteininteractionnetworks