Mackiewicz Paweł, Wyroba Elzbieta
University of Wrocław, Faculty of Biotechnology, Department of Genomics, 63/77 Przybyszewskiego Street, 51-148 Wrocław, Poland.
BMC Evol Biol. 2009 May 14;9:101. doi: 10.1186/1471-2148-9-101.
An important role in the evolution of intracellular trafficking machinery in eukaryotes played small GTPases belonging to the Rab family known as pivotal regulators of vesicle docking, fusion and transport. The Rab family is very diversified and divided into several specialized subfamilies. We focused on the VII functional group comprising Rab7 and Rab9, two related subfamilies, and analysed 210 sequences of these proteins. Rab7 regulates traffic from early to late endosomes and from late endosome to vacuole/lysosome, whereas Rab9 participates in transport from late endosomes to the trans-Golgi network.
Although Rab7 and Rab9 proteins are quite small and show heterogeneous rates of substitution in different lineages, we found a phylogenetic signal and inferred evolutionary relationships between them. Rab7 proteins evolved before radiation of main eukaryotic supergroups while Rab9 GTPases diverged from Rab7 before split of choanoflagellates and metazoans. Additional duplication of Rab9 and Rab7 proteins resulting in several isoforms occurred in the early evolution of vertebrates and next in teleost fishes and tetrapods. Three Rab7 lineages emerged before divergence of monocots and eudicots and subsequent duplications of Rab7 genes occurred in particular angiosperm clades. Interestingly, several Rab7 copies were identified in some representatives of excavates, ciliates and amoebozoans. The presence of many Rab copies is correlated with significant differences in their expression level. The diversification of analysed Rab subfamilies is also manifested by non-conserved sequences and structural features, many of which are involved in the interaction with regulators and effectors. Individual sites discriminating different subgroups of Rab7 and Rab9 GTPases have been identified.
Phylogenetic reconstructions of Rab7 and Rab9 proteins were performed by a variety of methods. These Rab GTPases show diversification both at the phylogenetic, expression and structural levels. The presence of many Rab7 and Rab9 isoforms suggests their functional specialization and complexity of subcellular trafficking even in unicellular eukaryotes. The identified less conserved regions in analysed Rab sequences may directly contribute to such a differentiation.
属于Rab家族的小GTP酶在真核生物细胞内运输机制的进化中发挥了重要作用,它们被认为是囊泡对接、融合和运输的关键调节因子。Rab家族非常多样化,分为几个专门的亚家族。我们聚焦于由Rab7和Rab9组成的VII功能组,这两个亚家族相关,并分析了这些蛋白质的210个序列。Rab7调节从早期内体到晚期内体以及从晚期内体到液泡/溶酶体的运输,而Rab9参与从晚期内体到反式高尔基体网络的运输。
尽管Rab7和Rab9蛋白相当小,并且在不同谱系中显示出异质的替换率,但我们发现了一个系统发育信号,并推断出它们之间的进化关系。Rab7蛋白在主要真核超群辐射之前就已进化,而Rab9 GTP酶在领鞭毛虫和后生动物分裂之前就与Rab7分化。Rab9和Rab7蛋白的额外复制导致了几种异构体,这发生在脊椎动物的早期进化中,随后在硬骨鱼和四足动物中出现。三个Rab7谱系在单子叶植物和双子叶植物分化之前出现,随后Rab7基因的复制发生在特定的被子植物分支中。有趣的是,在一些掘足动物、纤毛虫和变形虫的代表中发现了几个Rab7拷贝。许多Rab拷贝的存在与它们表达水平的显著差异相关。分析的Rab亚家族的多样化也表现为非保守序列和结构特征,其中许多参与了与调节因子和效应器的相互作用。已经确定了区分Rab7和Rab9 GTP酶不同亚组的个别位点。
通过多种方法对Rab7和Rab9蛋白进行了系统发育重建。这些Rab GTP酶在系统发育、表达和结构水平上都表现出多样化。许多Rab7和Rab9异构体的存在表明它们的功能特化以及即使在单细胞真核生物中亚细胞运输的复杂性。在分析的Rab序列中确定的较少保守区域可能直接促成了这种分化。