ArticleBMC systems biology2010
Understanding protein evolutionary rate by integrating gene co-expression with protein interactions.
Article in BMC systems biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Predictors of Protein Evolution in the drosophilid Immune System.Genome biology and evolution · 2026Article
- Characterizing lineage-specific evolution and the processes driving genomic diversification in chordates.BMC evolutionary biology · 2020Article
- Prediction of Protein-Protein Interactions by Evidence Combining Methods.International journal of molecular sciences · 2016Review
- Intermediate divergence levels maximize the strength of structure-sequence correlations in enzymes and viral proteins.Protein science : a publication of the Protein Society · 2016Article
- Relationship between protein thermodynamic constraints and variation of evolutionary rates among sites.Physical biology · 2015Article
- Predicting the binding patterns of hub proteins: a study using yeast protein interaction networks.PloS one · 2013Article
- Assessing the utility of gene co-expression stability in combination with correlation in the analysis of protein-protein interaction networks.BMC genomics · 2011Article
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Authors and funding
5 authors.
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Abstract
backgroundAmong the many factors determining protein evolutionary rate, protein-protein interaction degree (PPID) has been intensively investigated in recent years, but its precise effect on protein evolutionary rate is still heavily debated.
resultsWe first confirmed that the correlation between protein evolutionary rate and PPID varies considerably across different protein interaction datasets. Specifically, because of the maximal inconsistency between yeast two-hybrid and other datasets, we reasoned that the difference in experimental methods contributes to our inability to clearly define how PPID affects protein evolutionary rate. To address this, we integrated protein interaction and gene co-expression data to derive a co-expressed protein-protein interaction degree (ePPID) measure, which reflects the number of partners with which a protein can permanently interact. Thus, irrespective of the experimental method employed, we found that (1) ePPID is a better predictor of protein evolutionary rate than PPID, (2) ePPID is a more robust predictor of protein evolutionary rate than PPID, and (3) the contribution of ePPID to protein evolutionary rate is statistically independent of expression level. Analysis of hub proteins in the Structural Interaction Network further supported ePPID as a better predictor of protein evolutionary rate than the number of distinct binding interfaces and clarified the slower evolution of co-expressed multi-interface hub proteins over that of other hub proteins.
conclusionsOur study firmly established ePPID as a robust predictor of protein evolutionary rate, irrespective of experimental method, and underscored the importance of permanent interactions in shaping the evolutionary outcome.
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