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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,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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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. |
format | Online Article Text |
id | pubmed-7519090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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