Bharathi V, Pallavi S K, Bajpai R, Emerald B S, Shashidhara L S
Centre for Cellular and Molecular Biology, Uppal Road, Hyderabad, India 500 007.
J Cell Sci. 2004 Apr 15;117(Pt 10):1911-22. doi: 10.1242/jcs.01034.
We report cloning and characterization of coro, which codes for the Drosophila homologue of the F-actin binding protein coronin. Viable alleles of coro produce a variety of phenotypes in leg, wing and eye development, which are similar to the phenotypes observed as a result of mutations in genes associated with the actin cytoskeleton and/or membrane trafficking. Homozygous lethal mutations in coro results in the disruption of the actin cytoskeleton in wing imaginal discs. Formation of both basolateral septate junctions and apical adherens junctions are also adversely affected in epithelial cells. Both viable and lethal alleles of coro show genetic interactions with syntaxin1A, a gene required for membrane trafficking. They also show enhanced response to over-expression of Decapentaplegic (Dpp) and its receptor Thick vein. Tracing of Dpp morphogen using a Dpp::GFP fusion construct suggested defects in the endocytic pathway, which resulted in uniform distribution of Dpp along the AP axis rather than a gradient from the AP boundary. Our results provide a genetic link between endocytosis/exocytosis events involving F actin-coated vesicles and the establishment of morphogen gradient.
我们报道了coro的克隆和特征分析,它编码果蝇中F-肌动蛋白结合蛋白冠蛋白的同源物。coro的可行等位基因在腿部、翅膀和眼睛发育中产生多种表型,这些表型与因肌动蛋白细胞骨架和/或膜运输相关基因突变而观察到的表型相似。coro中的纯合致死突变导致翅成虫盘肌动蛋白细胞骨架的破坏。上皮细胞中基底外侧分隔连接和顶端黏附连接的形成也受到不利影响。coro的可行和致死等位基因均与膜运输所需的基因Syntaxin1A表现出遗传相互作用。它们还显示出对过表达的Decapentaplegic(Dpp)及其受体Thick vein的反应增强。使用Dpp::GFP融合构建体追踪Dpp形态发生素表明内吞途径存在缺陷,这导致Dpp沿前后轴均匀分布,而不是从前-后边界形成梯度。我们的结果提供了涉及F-肌动蛋白包被囊泡的内吞/外排事件与形态发生素梯度建立之间的遗传联系。