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Evolutionary Divergence of Phosphorylation to Regulate Interactive Protein Networks in Lower and Higher Species
The phosphorylation of proteins affects their functions in extensively documented circumstances. However, the role of phosphorylation in many interactive networks of proteins remains very elusive due to the experimental limits of exploring the transient interaction in a large complex of assembled pr...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9697241/ https://www.ncbi.nlm.nih.gov/pubmed/36430905 http://dx.doi.org/10.3390/ijms232214429 |
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author | Pasquier, Claude Robichon, Alain |
author_facet | Pasquier, Claude Robichon, Alain |
author_sort | Pasquier, Claude |
collection | PubMed |
description | The phosphorylation of proteins affects their functions in extensively documented circumstances. However, the role of phosphorylation in many interactive networks of proteins remains very elusive due to the experimental limits of exploring the transient interaction in a large complex of assembled proteins induced by stimulation. Previous studies have suggested that phosphorylation is a recent evolutionary process that differently regulates ortholog proteins in numerous lineages of living organisms to create new functions. Despite the fact that numerous phospho-proteins have been compared between species, little is known about the organization of the full phospho-proteome, the role of phosphorylation to orchestrate large interactive networks of proteins, and the intertwined phospho-landscape in these networks. In this report, we aimed to investigate the acquired role of phosphate addition in the phenomenon of protein networking in different orders of living organisms. Our data highlighted the acquired status of phosphorylation in organizing large, connected assemblages in Homo sapiens. The protein networking guided by phosphorylation turned out to be prominent in humans, chaotic in yeast, and weak in flies. Furthermore, the molecular functions of GO annotation enrichment regulated by phosphorylation were found to be drastically different between flies, yeast, and humans, suggesting an evolutionary drift specific to each species. |
format | Online Article Text |
id | pubmed-9697241 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96972412022-11-26 Evolutionary Divergence of Phosphorylation to Regulate Interactive Protein Networks in Lower and Higher Species Pasquier, Claude Robichon, Alain Int J Mol Sci Article The phosphorylation of proteins affects their functions in extensively documented circumstances. However, the role of phosphorylation in many interactive networks of proteins remains very elusive due to the experimental limits of exploring the transient interaction in a large complex of assembled proteins induced by stimulation. Previous studies have suggested that phosphorylation is a recent evolutionary process that differently regulates ortholog proteins in numerous lineages of living organisms to create new functions. Despite the fact that numerous phospho-proteins have been compared between species, little is known about the organization of the full phospho-proteome, the role of phosphorylation to orchestrate large interactive networks of proteins, and the intertwined phospho-landscape in these networks. In this report, we aimed to investigate the acquired role of phosphate addition in the phenomenon of protein networking in different orders of living organisms. Our data highlighted the acquired status of phosphorylation in organizing large, connected assemblages in Homo sapiens. The protein networking guided by phosphorylation turned out to be prominent in humans, chaotic in yeast, and weak in flies. Furthermore, the molecular functions of GO annotation enrichment regulated by phosphorylation were found to be drastically different between flies, yeast, and humans, suggesting an evolutionary drift specific to each species. MDPI 2022-11-20 /pmc/articles/PMC9697241/ /pubmed/36430905 http://dx.doi.org/10.3390/ijms232214429 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pasquier, Claude Robichon, Alain Evolutionary Divergence of Phosphorylation to Regulate Interactive Protein Networks in Lower and Higher Species |
title | Evolutionary Divergence of Phosphorylation to Regulate Interactive Protein Networks in Lower and Higher Species |
title_full | Evolutionary Divergence of Phosphorylation to Regulate Interactive Protein Networks in Lower and Higher Species |
title_fullStr | Evolutionary Divergence of Phosphorylation to Regulate Interactive Protein Networks in Lower and Higher Species |
title_full_unstemmed | Evolutionary Divergence of Phosphorylation to Regulate Interactive Protein Networks in Lower and Higher Species |
title_short | Evolutionary Divergence of Phosphorylation to Regulate Interactive Protein Networks in Lower and Higher Species |
title_sort | evolutionary divergence of phosphorylation to regulate interactive protein networks in lower and higher species |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9697241/ https://www.ncbi.nlm.nih.gov/pubmed/36430905 http://dx.doi.org/10.3390/ijms232214429 |
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