Rab protein evolution and the history of the eukaryotic endomembrane system

被引:67
作者
Brighouse, Andrew [1 ,2 ]
Dacks, Joel B. [3 ]
Field, Mark C. [1 ]
机构
[1] Univ Cambridge, Dept Pathol, Cambridge CB2 1QP, England
[2] Kings Coll London Sch Med, London SE1 1UL, England
[3] Univ Alberta, Dept Cell Biol, Edmonton, AB T6G 2H7, Canada
基金
加拿大自然科学与工程研究理事会; 英国惠康基金;
关键词
Trafficking; Evolution; Eukaryogenesis; Rab protein; Systems biology; MEMBRANE-FUSION; ENDOPLASMIC-RETICULUM; TRYPANOSOMA-BRUCEI; STRUCTURAL BASIS; ESCORT PROTEIN; GTPASE FAMILY; LIPID RAFTS; TRAFFICKING; DOMAIN; ENDOCYTOSIS;
D O I
10.1007/s00018-010-0436-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Spectacular increases in the quantity of sequence data genome have facilitated major advances in eukaryotic comparative genomics. By exploiting homology with classical model organisms, this makes possible predictions of pathways and cellular functions currently impossible to address in intractable organisms. Echoing realization that core metabolic processes were established very early following evolution of life on earth, it is now emerging that many eukaryotic cellular features, including the endomembrane system, are ancient and organized around near-universal principles. Rab proteins are key mediators of vesicle transport and specificity, and via the presence of multiple paralogues, alterations in interaction specificity and modification of pathways, contribute greatly to the evolution of complexity of membrane transport. Understanding system-level contributions of Rab proteins to evolutionary history provides insight into the multiple processes sculpting cellular transport pathways and the exciting challenges that we face in delving further into the origins of membrane trafficking specificity.
引用
收藏
页码:3449 / 3465
页数:17
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