Signaling from Ras to Rac and beyond: not just a matter of GEFs

被引:184
作者
Scita, G [1 ]
Tenca, P [1 ]
Frittoli, E [1 ]
Tocchetti, A [1 ]
Innocenti, M [1 ]
Giardina, G [1 ]
Di Fiore, PP [1 ]
机构
[1] European Inst Oncol, Dept Expt Oncol, I-20141 Milan, Italy
关键词
GEFs; Rac; Ras; Rho-GTPases; signal transduction;
D O I
10.1093/emboj/19.11.2393
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
Members of a family of intracellular molecular switches, the small GTPases, sense modifications of the extracellular environment and transduce them into a variety of homeostatic signals. Among small GTPases, Ras and the Rho family of proteins hierarchically and/or coordinately regulate signaling pathways leading to phenotypes as important as proliferation, differentiation and apoptosis, Ras and Rho-GTPases are organized in a complex network of functional interactions, whose molecular mechanisms are being elucidated. Starting from the simple concept of linear cascades of events (GTPase-->activator-->GTPase), the work of several laboratories is uncovering an increasingly complex scenario in which upstream regulators of GTPases also function as downstream effecters and influence the precise biological outcome. Furthermore, small GTPases assemble into macromolecular machineries that include upstream activators, downstream effecters, regulators and perhaps even final biochemical targets, We are starting to understand how these macromolecular complexes work and how they are regulated and targeted to their proper subcellular localization. Ultimately, the acquisition of a cogent picture of the various levels of integration and regulation in small GTPase-mediated signaling should define the physiology of early signal transduction events and the pathological implication of its subversion.
引用
收藏
页码:2393 / 2398
页数:6
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