Ozasa Fumito, Morishita Kazushige, Dang Ngoc Anh Suong, Miyata Seiji, Yoshida Hideki, Yamaguchi Masamitsu
Department of Applied Biology, The Center for Advanced Insect Research, Kyoto Institute of Technology.
Cell Struct Funct. 2017 Aug 26;42(2):117-129. doi: 10.1247/csf.17014. Epub 2017 Jul 13.
The dedicator of cytokinesis (DOCK) family proteins are known as one of guanine nucleotide exchange factors (GEFs), that contribute to cellular signaling processes by activating small G proteins. Although mammalian Zizimin is known to be a GEF for Cdc42 of Rho family small GTPase, its role in vivo is not well understood. Here we studied in vivo function of Drosophila Zizimin (Ziz). Knockdown of Ziz in eye imaginal discs induced the rough eye phenotype accompanied with fusion of ommatidia, loss of bristles and loss of pigments. Immunostaining analyses revealed that Ziz mainly localizes in the secondary pigment cells (SPCs) and tertiary pigment cells (TPCs) in pupal retinae. Ziz-knockdown induced SPC- and TPC-like cells with aberrant morphology in the pupal retina. Delta (Dl), a downstream target of EGFR signaling is known to regulate pigment cell differentiation. Loss-of-function mutation of Dl suppressed the rough eye phenotype and the defect in differentiation of SPCs and TPCs in Ziz-knockdown flies. Moreover, Ziz-knockdown increased Dl expression level especially in SPCs and TPCs. In addition, mutations of rhomboid-1 and roughoid that are activators of EGFR signaling pathway also suppressed both the rough eye phenotype and the defect in differentiation of SPCs and TPCs in Ziz-knockdown flies. Activation of EGFR signaling in Ziz-knockdown flies were further confirmed by immunostaining with anti-diphospho ERK IgG. These results indicate that Ziz negatively regulates the Dl expression in SPCs and TPCs to control differentiation of pigment cells and this regulation is mediated by EGFR signaling pathway.Key words: Zizimin, DOCK, EGFR signaling pathway, pigment cell, Drosophila.
胞质分裂 dedicator(DOCK)家族蛋白是鸟嘌呤核苷酸交换因子(GEF)之一,通过激活小 G 蛋白促进细胞信号传导过程。尽管已知哺乳动物的 Zizimin 是 Rho 家族小 GTP 酶 Cdc42 的 GEF,但其在体内的作用尚不清楚。在这里,我们研究了果蝇 Zizimin(Ziz)的体内功能。在眼成虫盘中敲低 Ziz 会诱导粗糙眼表型,伴有小眼融合、刚毛缺失和色素缺失。免疫染色分析表明,Ziz 主要定位于蛹视网膜中的次生色素细胞(SPC)和三生色素细胞(TPC)。敲低 Ziz 会在蛹视网膜中诱导出形态异常的 SPC 样和 TPC 样细胞。Delta(Dl)是 EGFR 信号的下游靶点,已知其可调节色素细胞分化。Dl 的功能丧失突变抑制了粗糙眼表型以及敲低 Ziz 的果蝇中 SPC 和 TPC 分化的缺陷。此外,敲低 Ziz 会增加 Dl 的表达水平,尤其是在 SPC 和 TPC 中。此外,EGFR 信号通路激活剂 rhomboid-1 和 roughoid 的突变也抑制了敲低 Ziz 的果蝇中的粗糙眼表型以及 SPC 和 TPC 分化的缺陷。用抗二磷酸化 ERK IgG 进行免疫染色进一步证实了敲低 Ziz 的果蝇中 EGFR 信号的激活。这些结果表明,Ziz 通过负调节 SPC 和 TPC 中 Dl 的表达来控制色素细胞的分化,并且这种调节是由 EGFR 信号通路介导的。关键词:Zizimin、DOCK、EGFR 信号通路、色素细胞、果蝇