首页> 外文期刊>Cell >A Centrosomal Cdc20-APC Pathway Controls Dendrite Morphogenesis in Postmitotic Neurons
【24h】

A Centrosomal Cdc20-APC Pathway Controls Dendrite Morphogenesis in Postmitotic Neurons

机译:中央Cdc20 APC通路控制有丝分裂后神经元中的树突形态发生。

获取原文
获取原文并翻译 | 示例
           

摘要

The ubiquitin ligase anaphase-promoting complex (APC) recruits the coactivator Cdc20 to drive mitosis in cycling cells. However, the nonmitotic functions of Cdc20-APC have remained unexplored. We report that Cdc20-APC plays an essential role in dendrite morphogenesis in postmitotic neurons. Knockdown of Cdc20 in cerebellar slices and in postnatal rats in vivo profoundly impairs the formation of granule neuron dendrite arbors in the cerebellar cortex. Remarkably, Cdc20 is enriched at the centrosome in neurons, and the centrosomal localization is.crit-ical for Cdc20-dependent dendrite development. We also find that the centrosome-associated protein histone deacetylase 6 (HDAC6) promotes the poly-ubiquitination of Cdc20, stimulates the activity of centrosomal Cdc20-APC, and drives the differentiation of dendrites. These findings define a postmitotic function for Cdc20-APC in the morphogenesis of dendrites in the mammalian brain. The identification of a centrosomal Cdc20-APC ubiquitin signaling pathway holds important implications for diverse biological processes, including neuronal connec_tivity and plasticity.
机译:泛素连接酶后期促进复合物(APC)募集辅助激活剂Cdc20以驱动循环细胞中的有丝分裂。但是,Cdc20-APC的非有丝分裂功能尚未开发。我们报道Cdc20 APC在有丝分裂后神经元的树突形态发生中起重要作用。在体内小脑切片和产后大鼠中敲除Cdc20会严重损害小脑皮层中颗粒神经元树突状乔木的形成。值得注意的是,Cdc20在神经元的中心体富集,中心体定位对于依赖Cdc20的枝晶发育至关重要。我们还发现,与中心体相关的蛋白组蛋白脱乙酰基酶6(HDAC6)促进Cdc20的多聚泛素化,刺激中心体Cdc20-APC的活性,并驱动树突的分化。这些发现定义了Cdc20-APC在哺乳动物脑中树突的形态发生中的有丝分裂后功能。中心体Cdc20-APC泛素信号通路的鉴定对包括神经元连接性和可塑性在内的多种生物过程具有重要意义。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号