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Coevolution is a short-distance force at the protein interaction level and correlates with the modular organization of protein networks
Authors:Zhi Liang  Meng Xu  Maikun Teng  Jiarui Wu
Affiliation:a Hefei National Laboratory for Physical Sciences at Microscale and School of Life Science, University of Science & Technology of China, Hefei, Anhui 230027, China
b Key Laboratory of Systems Biology, State Key Laboratory of Molecular Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 320 Yue-Yang Road, Shanghai 200031, China
Abstract:
We investigated what roles coevolution plays in shaping yeast protein interaction network (PIN). We found that the extent of coevolution between two proteins decreases rapidly as their interacting distance on the PIN increases, suggesting coevolutionary constraint is a short-distance force at the molecular level. We also found that protein-protein interactions (PPIs) with strong coevolution tend to be enriched in interconnected clusters, whereas PPIs with weak coevolution are more frequently present at inter-cluster region. The findings indicate the close relationship between coevolution and modular organization of PINs, and may provide insights into evolution and modularity of cellular networks.
Keywords:PPI, protein-protein interaction   PIN, protein interaction network   MYP, merged yeast PIN   PCC, Pearson correlation coefficient
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