Department of Cell Biology, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Canada.
School of Life Sciences, University of Dundee, Dundee, UK.
Traffic. 2018 Jul;19(7):546-563. doi: 10.1111/tra.12570. Epub 2018 Apr 25.
Endocytosis is a crucial process in eukaryotic cells. The GTPases Rab 5, 21 and 22 that mediate endocytosis are ancient eukaryotic features and all available evidence suggests retained conserved function. In animals and fungi, these GTPases are regulated in part by proteins possessing Vps9 domains. However, the diversity, evolution and functions of Vps9 proteins beyond animals or fungi are poorly explored. Here we report a comprehensive analysis of the Vps9 family of GTPase regulators, combining molecular evolutionary data with functional characterization in the non-opisthokont model organism Trypanosoma brucei. At least 3 subfamilies, Alsin, Varp and Rabex5 + GAPVD1, are found across eukaryotes, suggesting that all are ancient features of regulation of endocytic Rab protein function. There are examples of lineage-specific Vps9 subfamily member expansions and novel domain combinations, suggesting diversity in precise regulatory mechanisms between individual lineages. Characterization of the Rabex5 + GAPVD1 and Alsin orthologues in T. brucei demonstrates that both proteins are involved in endocytosis, and that simultaneous knockdown prevents membrane recruitment of Rab5 and Rab21, indicating conservation of function. These data demonstrate that, for the Vps9-domain family at least, modulation of Rab function is mediated by evolutionarily conserved protein-protein interactions.
内吞作用是真核细胞的一个关键过程。介导内吞作用的 GTPase Rab5、21 和 22 是古老的真核特征,所有现有证据表明它们保留了保守的功能。在动物和真菌中,这些 GTPases 的部分功能受到具有 Vps9 结构域的蛋白质的调节。然而,Vps9 蛋白在动物或真菌之外的多样性、进化和功能仍未得到充分探索。在这里,我们报告了对 GTPase 调节剂 Vps9 家族的全面分析,结合分子进化数据和在非后口动物模式生物锥虫中的功能特征。在真核生物中至少发现了 3 个子家族,即 Alsin、Varp 和 Rabex5+GAPVD1,这表明它们都是调节内吞作用 Rab 蛋白功能的古老特征。存在谱系特异性 Vps9 子家族成员扩展和新的结构域组合的例子,表明在不同谱系之间存在精确调控机制的多样性。在 T. brucei 中对 Rabex5+GAPVD1 和 Alsin 同源物的表征表明,这两种蛋白质都参与了内吞作用,并且同时敲低会阻止 Rab5 和 Rab21 的膜募集,表明功能保守。这些数据表明,至少对于 Vps9 结构域家族而言,Rab 功能的调节是由进化保守的蛋白质-蛋白质相互作用介导的。