Gao F B, Brenman J E, Jan L Y, Jan Y N
Howard Hughes Medical Institute, Departments of Physiology and Biochemistry, University of California at San Francisco, San Francisco, California 94143-0725, USA.
Genes Dev. 1999 Oct 1;13(19):2549-61. doi: 10.1101/gad.13.19.2549.
Signaling between neurons requires highly specialized subcellular structures, including dendrites and axons. Dendrites exhibit diverse morphologies yet little is known about the mechanisms controlling dendrite formation in vivo. We have developed methods to visualize the stereotyped dendritic morphogenesis in living Drosophila embryos. Dendrite development is altered in prospero mutants and in transgenic embryos expressing a constitutively active form of the small GTPase cdc42. From a genetic screen, we have identified several genes that control different aspects of dendrite development including dendritic outgrowth, branching, and routing. These genes include kakapo, a large cytoskeletal protein related to plectin and dystrophin; flamingo, a seven-transmembrane protein containing cadherin-like repeats; enabled, a substrate of the tyrosine kinase Abl; and nine potentially novel loci. These findings begin to reveal the molecular mechanisms controlling dendritic morphogenesis.
神经元之间的信号传导需要高度特化的亚细胞结构,包括树突和轴突。树突呈现出多样的形态,但对于体内控制树突形成的机制却知之甚少。我们已经开发出方法来可视化活体果蝇胚胎中刻板的树突形态发生过程。在prospero突变体以及表达持续激活形式的小GTP酶cdc42的转基因胚胎中,树突发育发生了改变。通过遗传筛选,我们鉴定出了几个控制树突发育不同方面的基因,包括树突生长、分支和路径选择。这些基因包括kakapo,一种与网蛋白和肌营养不良蛋白相关的大型细胞骨架蛋白;flamingo,一种含有钙黏蛋白样重复序列的七次跨膜蛋白;enabled,酪氨酸激酶Abl的底物;以及九个潜在的新基因座。这些发现开始揭示控制树突形态发生的分子机制。