Department of Life Sciences, National Institute for Biotechnology, Negev, Israel.
Proc Natl Acad Sci U S A. 2012 Feb 14;109(7):E406-14. doi: 10.1073/pnas.1108633109. Epub 2012 Jan 17.
The structure and connectivity of protein-protein interaction (PPI) networks are maintained throughout evolution by coordinated changes (coevolution) of network proteins. Despite extensive research, relatively little is known regarding the molecular basis and functional implications of the coevolution of PPI networks. Here, we used proliferating cell nuclear antigen, a hub protein that mediates DNA replication and repair in eukaryotes, as a model system to study the coevolution of PPI networks in fungi. Using a combined bioinformatics and experimental approach, we discovered that PCNA-partner interactions tightly coevolved in fungal species, leading to specific modes of recognition. We found that fungal proliferating cell nuclear antigen-partner interaction networks diverged into two distinct groups as a result of such coevolution and that hybrid networks of these groups are functionally noncompatible in Saccharomyces cerevisiae. Our results indicate that the coevolution of PPI networks can form functional barriers between fungal species, and thus can promote and fix speciation.
蛋白质-蛋白质相互作用(PPI)网络的结构和连接性在进化过程中通过网络蛋白的协调变化(共进化)来维持。尽管进行了广泛的研究,但对于 PPI 网络共进化的分子基础和功能意义,人们知之甚少。在这里,我们使用增殖细胞核抗原(一种在真核生物中介导 DNA 复制和修复的枢纽蛋白)作为模型系统,研究真菌中 PPI 网络的共进化。我们采用了一种结合生物信息学和实验的方法,发现 PCNA-伙伴相互作用在真菌物种中紧密地共同进化,导致了特定的识别模式。我们发现,由于这种共进化,真菌增殖细胞核抗原-伙伴相互作用网络分为两个不同的组,而这些组的混合网络在酿酒酵母中功能上是不兼容的。我们的结果表明,PPI 网络的共进化可以在真菌物种之间形成功能障碍,从而促进和固定物种形成。