Department of Cell and Developmental Biology, Dental Research Institute, School of Dentistry, Seoul National University, Seoul 110-749, Korea.
Mol Cells. 2011 Nov;32(5):477-82. doi: 10.1007/s10059-011-0168-6. Epub 2011 Oct 21.
Sac1 phosphoinositide (PI) phosphatases are important regulators of PtdIns(4)P turnover at the ER, Golgi, and plasma membrane (PM) and are involved in diverse cellular processes including cytoskeletal organization and vesicular trafficking. Here, we present evidence that Sac1 regulates axon guidance in the embryonic CNS of Drosophila. Sac1 is expressed on three longitudinal axon tracts that are defined by the cell adhesion molecule Fasciclin II (Fas II). Mutations in the sac1 gene cause ectopic midline crossing of Fas II-positive axon tracts. This phenotype is rescued by neuronal expression of wild-type Sac1 but not by a catalytically-inactive mutant. Finally, sac1 displays dosage-sensitive genetic interactions with mutations in the genes that encode the midline repellent Slit and its axonal receptor Robo. Taken together, our results suggest that Sac1-mediated regulation of PIs is critical for Slit/Robo-dependent axon repulsion at the CNS midline.
Sac1 磷酸肌醇(PI)磷酸酶是内质网、高尔基体和质膜(PM)中 PtdIns(4)P 周转的重要调节剂,参与多种细胞过程,包括细胞骨架组织和囊泡运输。在这里,我们提供的证据表明 Sac1 调节果蝇胚胎中枢神经系统中的轴突导向。Sac1 在三个由细胞粘附分子 Fasciclin II(Fas II)定义的纵向轴突束上表达。Sac1 基因突变导致 Fas II 阳性轴突束的中线异位交叉。这种表型可以通过神经元表达野生型 Sac1 来挽救,但不能通过催化失活的突变体来挽救。最后,Sac1 与编码中线排斥物 Slit 及其轴突受体 Robo 的基因的突变表现出剂量敏感的遗传相互作用。总之,我们的结果表明,Sac1 介导的 PI 调节对于 Slit/Robo 依赖性轴突排斥在中枢神经系统中至关重要。