Department of Applied Biology, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto 606-8585, Japan.
Exp Cell Res. 2013 Aug 15;319(14):2179-95. doi: 10.1016/j.yexcr.2013.05.024. Epub 2013 Jun 5.
The Drosophila sponge (spg)/CG31048 gene belongs to the dedicator of cytokinesis (DOCK) family genes that are conserved in a wide variety of species. DOCK family members are known as DOCK1-DOCK11 in mammals. Although DOCK1 and DOCK2 involve neurite elongation and immunocyte differentiation, respectively, the functions of other DOCK family members are not fully understood. Spg is a Drosophila homolog of mammalian DOCK3 and DOCK4. Specific knockdown of spg by the GMR-GAL4 driver in eye imaginal discs induced abnormal eye morphology in adults. To mark the photoreceptor cells in eye imaginal discs, we used a set of enhancer trap strains that express lacZ in various sets of photoreceptor cells. Immunostaining with anti-Spg antibodies and anti-lacZ antibodies revealed that Spg is localized mainly in R7 photoreceptor cells. Knockdown of spg by the GMR-GAL4 driver reduced signals of R7 photoreceptor cells, suggesting involvement of Spg in R7 cell differentiation. Furthermore, immunostaining with anti-dpERK antibodies showed the level of activated ERK signal was reduced extensively by knockdown of spg in eye discs, and both the defects in eye morphology and dpERK signals were rescued by over-expression of the Drosophila raf gene, a component of the ERK signaling pathway. Furthermore, the Duolink in situ Proximity Ligation Assay method detected interaction signals between Spg and Rap1 in and around the plasma membrane of the eye disc cells. Together, these results indicate Spg positively regulates the ERK pathway that is required for R7 photoreceptor cell differentiation and the regulation is mediated by interaction with Rap1 during development of the compound eye.
果蝇海绵(spg)/CG31048 基因属于细胞分裂(DOCK)家族基因,该家族基因在多种物种中保守。DOCK 家族成员在哺乳动物中被称为 DOCK1-DOCK11。尽管 DOCK1 和 DOCK2 分别参与神经突伸长和免疫细胞分化,但其他 DOCK 家族成员的功能尚未完全阐明。Spg 是哺乳动物 DOCK3 和 DOCK4 的果蝇同源物。通过 GMR-GAL4 驱动子特异性敲低眼盘中的 spg,导致成虫中出现异常的眼睛形态。为了标记眼盘中的光感受器细胞,我们使用了一组增强子捕获株,这些株在各种光感受器细胞中表达 lacZ。用抗 Spg 抗体和抗 lacZ 抗体进行免疫染色显示,Spg 主要定位于 R7 光感受器细胞中。通过 GMR-GAL4 驱动子敲低 spg 降低了 R7 光感受器细胞的信号,表明 Spg 参与 R7 细胞分化。此外,用抗 dpERK 抗体进行免疫染色显示,在眼盘中敲低 spg 后,dpERK 信号的激活水平大大降低,并且通过过表达 ERK 信号通路的组成部分果蝇 raf 基因,可挽救眼睛形态和 dpERK 信号的缺陷。此外,Duolink 原位邻近连接分析方法检测到眼盘细胞的质膜内和周围的 Spg 和 Rap1 之间的相互作用信号。综上所述,这些结果表明 Spg 正向调节 ERK 通路,该通路对于 R7 光感受器细胞分化是必需的,并且该调节是通过发育过程中 Spg 与 Rap1 的相互作用介导的。