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共进化是蛋白质相互作用层面的短程力,与蛋白质网络的模块化组织相关。

Coevolution is a short-distance force at the protein interaction level and correlates with the modular organization of protein networks.

机构信息

Hefei National Laboratory for Physical Sciences at Microscale and School of Life Science, University of Science & Technology of China, Hefei, Anhui, China.

出版信息

FEBS Lett. 2010 Oct 8;584(19):4237-40. doi: 10.1016/j.febslet.2010.09.014. Epub 2010 Sep 17.

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.

摘要

我们研究了共同进化在塑造酵母蛋白质相互作用网络 (PIN) 中扮演的角色。我们发现,随着两个蛋白质在 PIN 上的相互作用距离增加,它们之间的共同进化程度迅速下降,这表明共同进化约束是分子水平上的短程力。我们还发现,具有强共同进化的蛋白质-蛋白质相互作用 (PPI) 往往富集在相互连接的簇中,而具有弱共同进化的 PPI 则更频繁地出现在簇间区域。这些发现表明共同进化与 PIN 的模块化组织之间存在密切关系,可能为细胞网络的进化和模块化提供新的见解。

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