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A simple dependence between protein evolution rate and the number of protein-protein interactions

BACKGROUND: It has been shown for an evolutionarily distant genomic comparison that the number of protein-protein interactions a protein has correlates negatively with their rates of evolution. However, the generality of this observation has recently been challenged. Here we examine the problem usin...

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Autores principales: Fraser, Hunter B, Wall, Dennis P, Hirsh, Aaron E
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC166126/
https://www.ncbi.nlm.nih.gov/pubmed/12769820
http://dx.doi.org/10.1186/1471-2148-3-11
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author Fraser, Hunter B
Wall, Dennis P
Hirsh, Aaron E
author_facet Fraser, Hunter B
Wall, Dennis P
Hirsh, Aaron E
author_sort Fraser, Hunter B
collection PubMed
description BACKGROUND: It has been shown for an evolutionarily distant genomic comparison that the number of protein-protein interactions a protein has correlates negatively with their rates of evolution. However, the generality of this observation has recently been challenged. Here we examine the problem using protein-protein interaction data from the yeast Saccharomyces cerevisiae and genome sequences from two other yeast species. RESULTS: In contrast to a previous study that used an incomplete set of protein-protein interactions, we observed a highly significant correlation between number of interactions and evolutionary distance to either Candida albicans or Schizosaccharomyces pombe. This study differs from the previous one in that it includes all known protein interactions from S. cerevisiae, and a larger set of protein evolutionary rates. In both evolutionary comparisons, a simple monotonic relationship was found across the entire range of the number of protein-protein interactions. In agreement with our earlier findings, this relationship cannot be explained by the fact that proteins with many interactions tend to be important to yeast. The generality of these correlations in other kingdoms of life unfortunately cannot be addressed at this time, due to the incompleteness of protein-protein interaction data from organisms other than S. cerevisiae. CONCLUSIONS: Protein-protein interactions tend to slow the rate at which proteins evolve. This may be due to structural constraints that must be met to maintain interactions, but more work is needed to definitively establish the mechanism(s) behind the correlations we have observed.
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spelling pubmed-1661262003-07-26 A simple dependence between protein evolution rate and the number of protein-protein interactions Fraser, Hunter B Wall, Dennis P Hirsh, Aaron E BMC Evol Biol Research Article BACKGROUND: It has been shown for an evolutionarily distant genomic comparison that the number of protein-protein interactions a protein has correlates negatively with their rates of evolution. However, the generality of this observation has recently been challenged. Here we examine the problem using protein-protein interaction data from the yeast Saccharomyces cerevisiae and genome sequences from two other yeast species. RESULTS: In contrast to a previous study that used an incomplete set of protein-protein interactions, we observed a highly significant correlation between number of interactions and evolutionary distance to either Candida albicans or Schizosaccharomyces pombe. This study differs from the previous one in that it includes all known protein interactions from S. cerevisiae, and a larger set of protein evolutionary rates. In both evolutionary comparisons, a simple monotonic relationship was found across the entire range of the number of protein-protein interactions. In agreement with our earlier findings, this relationship cannot be explained by the fact that proteins with many interactions tend to be important to yeast. The generality of these correlations in other kingdoms of life unfortunately cannot be addressed at this time, due to the incompleteness of protein-protein interaction data from organisms other than S. cerevisiae. CONCLUSIONS: Protein-protein interactions tend to slow the rate at which proteins evolve. This may be due to structural constraints that must be met to maintain interactions, but more work is needed to definitively establish the mechanism(s) behind the correlations we have observed. BioMed Central 2003-05-23 /pmc/articles/PMC166126/ /pubmed/12769820 http://dx.doi.org/10.1186/1471-2148-3-11 Text en Copyright © 2003 Fraser et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research Article
Fraser, Hunter B
Wall, Dennis P
Hirsh, Aaron E
A simple dependence between protein evolution rate and the number of protein-protein interactions
title A simple dependence between protein evolution rate and the number of protein-protein interactions
title_full A simple dependence between protein evolution rate and the number of protein-protein interactions
title_fullStr A simple dependence between protein evolution rate and the number of protein-protein interactions
title_full_unstemmed A simple dependence between protein evolution rate and the number of protein-protein interactions
title_short A simple dependence between protein evolution rate and the number of protein-protein interactions
title_sort simple dependence between protein evolution rate and the number of protein-protein interactions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC166126/
https://www.ncbi.nlm.nih.gov/pubmed/12769820
http://dx.doi.org/10.1186/1471-2148-3-11
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