Seabra Miguel C, Wasmeier Christina
Cell and Molecular Biology Section, Division of Biomedical Sciences, Faculty of Medicine, Imperial College London, London SW7 2AZ, UK.
Curr Opin Cell Biol. 2004 Aug;16(4):451-7. doi: 10.1016/j.ceb.2004.06.014.
The remarkable degree of specificity with which Rab GTPases recognise distinct subsets of intracellular membranes forms the basis of their ability to act as key cellular regulators, determining the recruitment of downstream effectors to the right membrane at the right time. The molecular mechanisms controlling Rab localisation, however, have proved tricky issues to address. It is becoming increasingly apparent that multiple factors contribute to the specificity of Rab localisation and the close coordination of membrane targeting with Rab activation. With important new insights into the mode of action of the general Rab regulators REP and RabGDI, as well as the demonstration that novel factors such as Yip3/Pra1 act as GDI displacement factors and that signals within Rab proteins contribute to targeting specificity, a better understanding of the concepts governing Rab recruitment and function is now beginning to emerge. The diversity of cellular processes regulated by Rab family members is made possible, not only by the wide range of effectors they recruit, but also by the different mechanisms regulating their own targeting and activation.
Rab GTP 酶识别细胞内膜不同亚群的显著特异性程度,构成了它们作为关键细胞调节因子发挥作用的基础,决定了下游效应器在正确的时间被招募到正确的膜上。然而,控制 Rab 定位的分子机制已被证明是难以解决的问题。越来越明显的是,多种因素促成了 Rab 定位的特异性以及膜靶向与 Rab 激活的紧密协调。随着对一般 Rab 调节因子 REP 和 RabGDI 作用模式的重要新见解,以及诸如 Yip3/Pra1 等新因子作为 GDI 置换因子的证明,以及 Rab 蛋白内的信号有助于靶向特异性,现在开始对控制 Rab 招募和功能的概念有了更好的理解。Rab 家族成员调节的细胞过程的多样性不仅通过它们招募的广泛效应器得以实现,还通过调节其自身靶向和激活的不同机制得以实现。