Fernández-Medarde Alberto, Santos Eugenio
Centro de Investigación del cáncer, IBMCC, University of Salamanca, 37007 Salamanca, Spain.
Biochim Biophys Acta. 2011 Apr;1815(2):170-88. doi: 10.1016/j.bbcan.2010.11.001. Epub 2010 Nov 25.
RasGrf1 and RasGrf2 are highly homologous mammalian guanine nucleotide exchange factors which are able to activate specific Ras or Rho GTPases. The RasGrf genes are preferentially expressed in the central nervous system, although specific expression of either locus may also occur elsewhere. RasGrf1 is a paternally-expressed, imprinted gene that is expressed only after birth. In contrast, RasGrf2 is not imprinted and shows a wider expression pattern. A variety of isoforms for both genes are also detectable in different cellular contexts. The RasGrf proteins exhibit modular structures composed by multiple domains including CDC25H and DHPH motifs responsible for promoting GDP/GTP exchange, respectively, on Ras or Rho GTPase targets. The various domains are essential to define their intrinsic exchanger activity and to modulate the specificity of their functional activity so as to connect different upstream signals to various downstream targets and cellular responses. Despite their homology, RasGrf1 and RasGrf2 display differing target specificities and non overlapping functional roles in a variety of signaling contexts related to cell growth and differentiation as well as neuronal excitability and response or synaptic plasticity. Whereas both RasGrfs are activatable by glutamate receptors, G-protein-coupled receptors or changes in intracellular calcium concentration, only RasGrf1 is reported to be activated by LPA, cAMP, or agonist-activated Trk and cannabinoid receptors. Analysis of various knockout mice strains has uncovered a specific functional contribution of RasGrf1 in processes of memory and learning, photoreception, control of post-natal growth and body size and pancreatic β-cell function and glucose homeostasis. For RasGrf2, specific roles in lymphocyte proliferation, T-cell signaling responses and lymphomagenesis have been described.
RasGrf1和RasGrf2是高度同源的哺乳动物鸟嘌呤核苷酸交换因子,能够激活特定的Ras或Rho GTP酶。RasGrf基因在中枢神经系统中优先表达,尽管任何一个基因座的特异性表达也可能在其他地方出现。RasGrf1是一个父本表达的印记基因,仅在出生后表达。相比之下,RasGrf2没有印记,表现出更广泛的表达模式。在不同的细胞环境中也可检测到这两个基因的多种同工型。RasGrf蛋白呈现出由多个结构域组成的模块化结构,包括分别负责促进Ras或Rho GTP酶靶点上GDP/GTP交换的CDC25H和DHPH基序。各个结构域对于定义其内在交换活性和调节其功能活性的特异性至关重要,以便将不同的上游信号连接到各种下游靶点和细胞反应。尽管RasGrf1和RasGrf2具有同源性,但在与细胞生长和分化以及神经元兴奋性、反应或突触可塑性相关的各种信号传导环境中,它们表现出不同的靶点特异性和非重叠的功能作用。虽然两种RasGrf都可被谷氨酸受体、G蛋白偶联受体或细胞内钙浓度变化激活,但据报道只有RasGrf1可被溶血磷脂酸(LPA)、环磷酸腺苷(cAMP)或激动剂激活的酪氨酸激酶受体(Trk)和大麻素受体激活。对各种基因敲除小鼠品系的分析揭示了RasGrf1在记忆和学习、光感受、出生后生长和体型控制以及胰腺β细胞功能和葡萄糖稳态过程中的特定功能贡献。对于RasGrf2,已描述了其在淋巴细胞增殖、T细胞信号反应和淋巴瘤发生中的特定作用。