Department of Molecular Genetics and Cell Biology, University of Chicago, Chicago, United States.
Program in Cell and Molecular Biology, University of Chicago, Chicago, United States.
Elife. 2020 May 11;9:e56898. doi: 10.7554/eLife.56898.
How circuit wiring is specified is a key question in developmental neurobiology. Previously, using the motor system as a model, we found the classic temporal transcription factor Hunchback acts in NB7-1 neuronal stem cells to control the number of NB7-1 neuronal progeny form functional synapses on dorsal muscles (Meng et al., 2019). However, it is unknown to what extent control of motor neuron-to-muscle synaptic partnerships is a general feature of temporal transcription factors. Here, we perform additional temporal transcription factor manipulations-prolonging expression of Hunchback in NB3-1, as well as precociously expressing Pdm and Castor in NB7-1. We use confocal microscopy, calcium imaging, and electrophysiology to show that in every manipulation there are permanent alterations in neuromuscular synaptic partnerships. Our data show temporal transcription factors, as a group of molecules, are potent determinants of synaptic partner choice and therefore ultimately control circuit membership.
神经回路如何布线是发育神经生物学的一个关键问题。此前,我们曾以运动系统为模型发现经典的时序转录因子 Hunchback 在 NB7-1 神经元干细胞中发挥作用,控制 NB7-1 神经元祖细胞形成功能性突触的数量,使其与背部肌肉连接(Meng 等人,2019 年)。然而,时序转录因子对运动神经元与肌肉突触连接的控制在多大程度上是普遍特征尚不清楚。在这里,我们进行了额外的时序转录因子操作——延长 NB3-1 中 Hunchback 的表达,以及在 NB7-1 中过早表达 Pdm 和 Castor。我们使用共聚焦显微镜、钙成像和电生理学显示,在每一种操作中,神经肌肉突触连接都发生了永久性改变。我们的数据表明,作为一组分子,时序转录因子是突触伙伴选择的有力决定因素,因此最终控制着回路的组成。