Cargando…

Assembly rules for protein networks derived from phylogenetic-statistical analysis of whole genomes

BACKGROUND: We report an analysis of a protein network of functionally linked proteins, identified from a phylogenetic statistical analysis of complete eukaryotic genomes. Phylogenetic methods identify pairs of proteins that co-evolve on a phylogenetic tree, and have been shown to have a high probab...

Descripción completa

Detalles Bibliográficos
Autores principales: Pagel, Mark, Meade, Andrew, Scott, Daniel
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1796610/
https://www.ncbi.nlm.nih.gov/pubmed/17288574
http://dx.doi.org/10.1186/1471-2148-7-S1-S16
_version_ 1782132243954663424
author Pagel, Mark
Meade, Andrew
Scott, Daniel
author_facet Pagel, Mark
Meade, Andrew
Scott, Daniel
author_sort Pagel, Mark
collection PubMed
description BACKGROUND: We report an analysis of a protein network of functionally linked proteins, identified from a phylogenetic statistical analysis of complete eukaryotic genomes. Phylogenetic methods identify pairs of proteins that co-evolve on a phylogenetic tree, and have been shown to have a high probability of correctly identifying known functional links. RESULTS: The eukaryotic correlated evolution network we derive displays the familiar power law scaling of connectivity. We introduce the use of explicit phylogenetic methods to reconstruct the ancestral presence or absence of proteins at the interior nodes of a phylogeny of eukaryote species. We find that the connectivity distribution of proteins at the point they arise on the tree and join the network follows a power law, as does the connectivity distribution of proteins at the time they are lost from the network. Proteins resident in the network acquire connections over time, but we find no evidence that 'preferential attachment' – the phenomenon of newly acquired connections in the network being more likely to be made to proteins with large numbers of connections – influences the network structure. We derive a 'variable rate of attachment' model in which proteins vary in their propensity to form network interactions independently of how many connections they have or of the total number of connections in the network, and show how this model can produce apparent power-law scaling without preferential attachment. CONCLUSION: A few simple rules can explain the topological structure and evolutionary changes to protein-interaction networks: most change is concentrated in satellite proteins of low connectivity and small phenotypic effect, and proteins differ in their propensity to form attachments. Given these rules of assembly, power law scaled networks naturally emerge from simple principles of selection, yielding protein interaction networks that retain a high-degree of robustness on short time scales and evolvability on longer evolutionary time scales.
format Text
id pubmed-1796610
institution National Center for Biotechnology Information
language English
publishDate 2007
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-17966102007-02-09 Assembly rules for protein networks derived from phylogenetic-statistical analysis of whole genomes Pagel, Mark Meade, Andrew Scott, Daniel BMC Evol Biol Research BACKGROUND: We report an analysis of a protein network of functionally linked proteins, identified from a phylogenetic statistical analysis of complete eukaryotic genomes. Phylogenetic methods identify pairs of proteins that co-evolve on a phylogenetic tree, and have been shown to have a high probability of correctly identifying known functional links. RESULTS: The eukaryotic correlated evolution network we derive displays the familiar power law scaling of connectivity. We introduce the use of explicit phylogenetic methods to reconstruct the ancestral presence or absence of proteins at the interior nodes of a phylogeny of eukaryote species. We find that the connectivity distribution of proteins at the point they arise on the tree and join the network follows a power law, as does the connectivity distribution of proteins at the time they are lost from the network. Proteins resident in the network acquire connections over time, but we find no evidence that 'preferential attachment' – the phenomenon of newly acquired connections in the network being more likely to be made to proteins with large numbers of connections – influences the network structure. We derive a 'variable rate of attachment' model in which proteins vary in their propensity to form network interactions independently of how many connections they have or of the total number of connections in the network, and show how this model can produce apparent power-law scaling without preferential attachment. CONCLUSION: A few simple rules can explain the topological structure and evolutionary changes to protein-interaction networks: most change is concentrated in satellite proteins of low connectivity and small phenotypic effect, and proteins differ in their propensity to form attachments. Given these rules of assembly, power law scaled networks naturally emerge from simple principles of selection, yielding protein interaction networks that retain a high-degree of robustness on short time scales and evolvability on longer evolutionary time scales. BioMed Central 2007-02-08 /pmc/articles/PMC1796610/ /pubmed/17288574 http://dx.doi.org/10.1186/1471-2148-7-S1-S16 Text en Copyright © 2007 Pagel et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Pagel, Mark
Meade, Andrew
Scott, Daniel
Assembly rules for protein networks derived from phylogenetic-statistical analysis of whole genomes
title Assembly rules for protein networks derived from phylogenetic-statistical analysis of whole genomes
title_full Assembly rules for protein networks derived from phylogenetic-statistical analysis of whole genomes
title_fullStr Assembly rules for protein networks derived from phylogenetic-statistical analysis of whole genomes
title_full_unstemmed Assembly rules for protein networks derived from phylogenetic-statistical analysis of whole genomes
title_short Assembly rules for protein networks derived from phylogenetic-statistical analysis of whole genomes
title_sort assembly rules for protein networks derived from phylogenetic-statistical analysis of whole genomes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1796610/
https://www.ncbi.nlm.nih.gov/pubmed/17288574
http://dx.doi.org/10.1186/1471-2148-7-S1-S16
work_keys_str_mv AT pagelmark assemblyrulesforproteinnetworksderivedfromphylogeneticstatisticalanalysisofwholegenomes
AT meadeandrew assemblyrulesforproteinnetworksderivedfromphylogeneticstatisticalanalysisofwholegenomes
AT scottdaniel assemblyrulesforproteinnetworksderivedfromphylogeneticstatisticalanalysisofwholegenomes