Fukuhara S, Chikumi H, Gutkind J S
Oral and Pharyngeal Cancer Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, 9000 Rockville Pike, Building 30, Room 211, Bethesda, MD 20892-4330, USA.
FEBS Lett. 2000 Nov 24;485(2-3):183-8. doi: 10.1016/s0014-5793(00)02224-9.
A putative guanine nucleotide exchange factor (GEF), termed leukemia-associated RhoGEF (LARG), was recently identified upon fusion to the coding sequence of the MLL gene in acute myeloid leukemia. Although the function of LARG is still unknown, it exhibits a number of structural domains suggestive of a role in signal transduction, including a PDZ domain, a LH/RGS domain, and a Dbl homology/pleckstrin homology domain. Here, we show that LARG can activate Rho in vivo. Furthermore, we present evidence that LARG is an integral component of a novel biochemical route whereby G protein-coupled receptors (GPCRs) and heterotrimeric G proteins of the G alpha(12) family stimulate Rho-dependent signaling pathways.
一种被认为是鸟嘌呤核苷酸交换因子(GEF)的蛋白,称为白血病相关RhoGEF(LARG),最近在急性髓系白血病中与MLL基因的编码序列融合时被鉴定出来。尽管LARG的功能仍不清楚,但它具有一些提示其在信号转导中起作用的结构域,包括一个PDZ结构域、一个LH/RGS结构域和一个Dbl同源/普列克底物蛋白同源结构域。在此,我们表明LARG在体内可激活Rho。此外,我们提供证据表明LARG是一条新的生化途径的重要组成部分,通过该途径,G蛋白偶联受体(GPCR)和Gα(12)家族的异源三聚体G蛋白可刺激Rho依赖性信号通路。