Evolutionary Rate in the Protein Interaction Network

High-throughput screens have begun to reveal the protein interaction network that underpins most cellular functions in the yeastSaccharomyces cerevisiae. How the organization of this network affects the evolution of the proteins that compose it is a fundamental question in molecular evolution. We show that the connectivity of well-conserved proteins in the network is negatively correlated with their rate of evolution. Proteins with more interactors evolve more slowly not because they are more important to the organism, but because a greater proportion of the protein is directly involved in its function. At sites important for interaction between proteins, evolutionary changes may occur largely by coevolution, in which substitutions in one protein result in selection pressure for reciprocal changes in interacting partners. We confirm one predicted outcome of this process—namely, that interacting proteins evolve at similar rates.

[1]  D Botstein,et al.  Genetic footprinting: a genomic strategy for determining a gene's function given its sequence. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[2]  D Botstein,et al.  Functional Analysis of the Genes of Yeast Chromosome V by Genetic Footprinting , 1996, Science.

[3]  Russell F. Doolittle,et al.  Converting Amino Acid Alignment Scores into Measures of Evolutionary Time: A Simulation Study of Various Relationships , 1997, Journal of Molecular Evolution.

[4]  J. Lake,et al.  Genomic evidence for two functionally distinct gene classes. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[5]  R. Burton,et al.  Isolation and characterization of cytochrome c from the marine copepod Tigriopus californicus. , 2000, Gene.

[6]  B. Schwikowski,et al.  A network of protein–protein interactions in yeast , 2000, Nature Biotechnology.

[7]  James R. Brown,et al.  Evolution of two-component signal transduction. , 2000, Molecular biology and evolution.

[8]  A. Grigoriev A relationship between gene expression and protein interactions on the proteome scale: analysis of the bacteriophage T7 and the yeast Saccharomyces cerevisiae. , 2001, Nucleic acids research.

[9]  A. Barabasi,et al.  Lethality and centrality in protein networks , 2001, Nature.

[10]  A. E. Hirsh,et al.  Protein dispensability and rate of evolution , 2001, Nature.

[11]  P. Bork,et al.  Functional organization of the yeast proteome by systematic analysis of protein complexes , 2002, Nature.

[12]  L. Kruglyak,et al.  Genetic Dissection of Transcriptional Regulation in Budding Yeast , 2002, Science.

[13]  Nick V. Grishin,et al.  Estimation of the number of amino acid substitutions per site when the substitution rate varies among sites , 1995, Journal of Molecular Evolution.