Lee S, Parent C A, Insall R, Firtel R A
Department of Biology, Center for Molecular Genetics, University of California, San Diego, La Jolla, California 92093-0634, USA.
Mol Biol Cell. 1999 Sep;10(9):2829-45. doi: 10.1091/mbc.10.9.2829.
We have identified a novel Ras-interacting protein from Dictyostelium, RIP3, whose function is required for both chemotaxis and the synthesis and relay of the cyclic AMP (cAMP) chemoattractant signal. rip3 null cells are unable to aggregate and lack receptor activation of adenylyl cyclase but are able, in response to cAMP, to induce aggregation-stage, postaggregative, and cell-type-specific gene expression in suspension culture. In addition, rip3 null cells are unable to properly polarize in a cAMP gradient and chemotaxis is highly impaired. We demonstrate that cAMP stimulation of guanylyl cyclase, which is required for chemotaxis, is reduced approximately 60% in rip3 null cells. This reduced activation of guanylyl cyclase may account, in part, for the defect in chemotaxis. When cells are pulsed with cAMP for 5 h to mimic the endogenous cAMP oscillations that occur in wild-type strains, the cells will form aggregates, most of which, however, arrest at the mound stage. Unlike the response seen in wild-type strains, the rip3 null cell aggregates that form under these experimental conditions are very small, which is probably due to the rip3 null cell chemotaxis defect. Many of the phenotypes of the rip3 null cell, including the inability to activate adenylyl cyclase in response to cAMP and defects in chemotaxis, are very similar to those of strains carrying a disruption of the gene encoding the putative Ras exchange factor AleA. We demonstrate that aleA null cells also exhibit a defect in cAMP-mediated activation of guanylyl cyclase similar to that of rip3 null cells. A double-knockout mutant (rip3/aleA null cells) exhibits a further reduction in receptor activation of guanylyl cyclase, and these cells display almost no cell polarization or movement in cAMP gradients. As RIP3 preferentially interacts with an activated form of the Dictyostelium Ras protein RasG, which itself is important for cell movement, we propose that RIP3 and AleA are components of a Ras-regulated pathway involved in integrating chemotaxis and signal relay pathways that are essential for aggregation.
我们从盘基网柄菌中鉴定出一种新型的Ras相互作用蛋白RIP3,趋化作用以及环磷酸腺苷(cAMP)趋化信号的合成与传递都需要其发挥功能。rip3基因缺失的细胞无法聚集,腺苷酸环化酶缺乏受体激活,但在悬浮培养中,它们能够响应cAMP诱导聚集期、聚集后以及细胞类型特异性基因表达。此外,rip3基因缺失的细胞无法在cAMP梯度中正确极化,趋化作用严重受损。我们证明,趋化作用所需的cAMP对鸟苷酸环化酶的刺激在rip3基因缺失的细胞中降低了约60%。鸟苷酸环化酶激活的降低可能部分解释了趋化作用的缺陷。当用cAMP脉冲处理细胞5小时以模拟野生型菌株中发生的内源性cAMP振荡时,细胞会形成聚集体,然而,其中大多数会在丘状阶段停滞。与野生型菌株中的反应不同,在这些实验条件下形成的rip3基因缺失细胞聚集体非常小,这可能是由于rip3基因缺失细胞的趋化缺陷。rip3基因缺失细胞的许多表型,包括无法响应cAMP激活腺苷酸环化酶以及趋化缺陷,与携带假定的Ras交换因子AleA编码基因破坏的菌株非常相似。我们证明,aleA基因缺失的细胞在cAMP介导的鸟苷酸环化酶激活方面也表现出与rip3基因缺失细胞类似的缺陷。双敲除突变体(rip3/aleA基因缺失细胞)在鸟苷酸环化酶的受体激活方面进一步降低,并且这些细胞在cAMP梯度中几乎没有细胞极化或移动。由于RIP3优先与盘基网柄菌Ras蛋白RasG的激活形式相互作用,而RasG本身对细胞运动很重要,我们提出RIP3和AleA是Ras调节途径的组成部分,该途径参与整合对聚集至关重要的趋化作用和信号传递途径。