Jiménez-Sánchez Alejandro
Cancer Research UK Cambridge Institute, University of Cambridge, Li Ka Shing Centre, Cambridge, UK.; Previously at Department of Biology, University of York, York, UK.
Evol Bioinform Online. 2016 May 17;12:121-31. doi: 10.4137/EBO.S38031. eCollection 2016.
RAC proteins are small GTPases involved in important cellular processes in eukaryotes, and their deregulation may contribute to cancer. Activation of RAC proteins is regulated by DOCK and DBL protein families of guanine nucleotide exchange factors (GEFs). Although DOCK and DBL proteins act as GEFs on RAC proteins, DOCK and DBL family members are evolutionarily unrelated. To understand how DBL and DOCK families perform the same function on RAC proteins despite their unrelated primary structure, phylogenetic analyses of the RAC, DBL, and DOCK families were implemented, and interaction patterns that may suggest a coevolutionary process were searched. Interestingly, while RAC and DOCK proteins are very well conserved in humans and among eukaryotes, DBL proteins are highly divergent. Moreover, correlation analyses of the phylogenetic distances of RAC and GEF proteins and covariation analyses between residues in the interacting domains showed significant coevolution rates for both RAC-DOCK and RAC-DBL interactions.
RAC蛋白是参与真核生物重要细胞过程的小GTP酶,其失调可能导致癌症。RAC蛋白的激活由鸟嘌呤核苷酸交换因子(GEF)的DOCK和DBL蛋白家族调节。尽管DOCK和DBL蛋白作为RAC蛋白的GEF发挥作用,但DOCK和DBL家族成员在进化上并无关联。为了理解DBL和DOCK家族尽管一级结构不相关却如何在RAC蛋白上执行相同功能,我们对RAC、DBL和DOCK家族进行了系统发育分析,并寻找可能暗示协同进化过程的相互作用模式。有趣的是,虽然RAC和DOCK蛋白在人类和真核生物中高度保守,但DBL蛋白却高度分化。此外,RAC和GEF蛋白系统发育距离的相关性分析以及相互作用结构域中残基之间的共变分析表明,RAC - DOCK和RAC - DBL相互作用均具有显著的协同进化速率。