Life Sciences Institute and Department of Cell and Developmental Biology, University of Michigan, Ann Arbor, Michigan 48109, USA.
J Neurosci. 2011 Mar 2;31(9):3309-19. doi: 10.1523/JNEUROSCI.6307-10.2011.
Dendrites and axons are two major neuronal compartments with differences that are critical for neuronal functions. To learn about the differential regulation of dendritic and axonal development, we conducted a genetic screen in Drosophila and isolated the dendritic arbor reduction 1 (dar1) mutants, which display defects in dendritic but not axonal growth. The dar1 gene encodes a novel transcription regulator in the Krüppel-like factor family. Neurons lacking dar1 function have severely reduced growth of microtubule- but not F-actin-based dendritic branches. In contrast, overexpression of Dar1 dramatically increased the growth of microtubule-based dendritic branches. Our results suggest that Dar1 promotes dendrite growth in part by suppressing the expression of the microtubule-severing protein Spastin. Our study thus uncovers a novel transcriptional program for microtubule regulation that preferentially controls dendrite growth.
树突和轴突是两种主要的神经元区室,它们之间的差异对神经元功能至关重要。为了了解树突和轴突发育的差异调节,我们在果蝇中进行了遗传筛选,分离出树突分支减少 1(dar1)突变体,该突变体表现出树突而非轴突生长的缺陷。dar1 基因编码 Krüppel 样因子家族中的一种新型转录调节因子。缺乏 dar1 功能的神经元的微管而非 F-肌动蛋白基树突分支的生长严重减少。相比之下,Dar1 的过表达显著增加了基于微管的树突分支的生长。我们的结果表明,Dar1 通过抑制微管切割蛋白 Spastin 的表达来促进树突生长。因此,我们的研究揭示了一个新的微管调节转录程序,该程序优先控制树突生长。