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Design principles of gene evolution for niche adaptation through changes in protein–protein interaction networks

In contrast to fossorial and above-ground organisms, subterranean species have adapted to the extreme stresses of living underground. We analyzed the predicted protein–protein interactions (PPIs) of all gene products, including those of stress-response genes, among nine subterranean, ten fossorial,...

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Autores principales: Carmi, Gon, Tagore, Somnath, Gorohovski, Alessandro, Sivan, Aviad, Raviv-Shay, Dorith, Frenkel-Morgenstern, Milana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519090/
https://www.ncbi.nlm.nih.gov/pubmed/32973219
http://dx.doi.org/10.1038/s41598-020-71976-x
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author Carmi, Gon
Tagore, Somnath
Gorohovski, Alessandro
Sivan, Aviad
Raviv-Shay, Dorith
Frenkel-Morgenstern, Milana
author_facet Carmi, Gon
Tagore, Somnath
Gorohovski, Alessandro
Sivan, Aviad
Raviv-Shay, Dorith
Frenkel-Morgenstern, Milana
author_sort Carmi, Gon
collection PubMed
description In contrast to fossorial and above-ground organisms, subterranean species have adapted to the extreme stresses of living underground. We analyzed the predicted protein–protein interactions (PPIs) of all gene products, including those of stress-response genes, among nine subterranean, ten fossorial, and 13 aboveground species. We considered 10,314 unique orthologous protein families and constructed 5,879,879 PPIs in all organisms using ChiPPI. We found strong association between PPI network modulation and adaptation to specific habitats, noting that mutations in genes and changes in protein sequences were not linked directly with niche adaptation in the organisms sampled. Thus, orthologous hypoxia, heat-shock, and circadian clock proteins were found to cluster according to habitat, based on PPIs rather than on sequence similarities. Curiously, "ordered" domains were preserved in aboveground species, while "disordered" domains were conserved in subterranean organisms, and confirmed for proteins in DistProt database. Furthermore, proteins with disordered regions were found to adopt significantly less optimal codon usage in subterranean species than in fossorial and above-ground species. These findings reveal design principles of protein networks by means of alterations in protein domains, thus providing insight into deep mechanisms of evolutionary adaptation, generally, and particularly of species to underground living and other confined habitats.
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spelling pubmed-75190902020-09-29 Design principles of gene evolution for niche adaptation through changes in protein–protein interaction networks Carmi, Gon Tagore, Somnath Gorohovski, Alessandro Sivan, Aviad Raviv-Shay, Dorith Frenkel-Morgenstern, Milana Sci Rep Article In contrast to fossorial and above-ground organisms, subterranean species have adapted to the extreme stresses of living underground. We analyzed the predicted protein–protein interactions (PPIs) of all gene products, including those of stress-response genes, among nine subterranean, ten fossorial, and 13 aboveground species. We considered 10,314 unique orthologous protein families and constructed 5,879,879 PPIs in all organisms using ChiPPI. We found strong association between PPI network modulation and adaptation to specific habitats, noting that mutations in genes and changes in protein sequences were not linked directly with niche adaptation in the organisms sampled. Thus, orthologous hypoxia, heat-shock, and circadian clock proteins were found to cluster according to habitat, based on PPIs rather than on sequence similarities. Curiously, "ordered" domains were preserved in aboveground species, while "disordered" domains were conserved in subterranean organisms, and confirmed for proteins in DistProt database. Furthermore, proteins with disordered regions were found to adopt significantly less optimal codon usage in subterranean species than in fossorial and above-ground species. These findings reveal design principles of protein networks by means of alterations in protein domains, thus providing insight into deep mechanisms of evolutionary adaptation, generally, and particularly of species to underground living and other confined habitats. Nature Publishing Group UK 2020-09-24 /pmc/articles/PMC7519090/ /pubmed/32973219 http://dx.doi.org/10.1038/s41598-020-71976-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Carmi, Gon
Tagore, Somnath
Gorohovski, Alessandro
Sivan, Aviad
Raviv-Shay, Dorith
Frenkel-Morgenstern, Milana
Design principles of gene evolution for niche adaptation through changes in protein–protein interaction networks
title Design principles of gene evolution for niche adaptation through changes in protein–protein interaction networks
title_full Design principles of gene evolution for niche adaptation through changes in protein–protein interaction networks
title_fullStr Design principles of gene evolution for niche adaptation through changes in protein–protein interaction networks
title_full_unstemmed Design principles of gene evolution for niche adaptation through changes in protein–protein interaction networks
title_short Design principles of gene evolution for niche adaptation through changes in protein–protein interaction networks
title_sort design principles of gene evolution for niche adaptation through changes in protein–protein interaction networks
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519090/
https://www.ncbi.nlm.nih.gov/pubmed/32973219
http://dx.doi.org/10.1038/s41598-020-71976-x
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