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Temporal transcription factors determine circuit membership by permanently altering motor neuron-to-muscle synaptic partnerships

Julia L Meng, Yupu Wang, Robert A. Carrillo, Ellie S. Heckscher

2020eLife28 citationsDOIOpen Access PDF

Abstract

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.

Topics & Concepts

NeuroscienceTranscription factorBiologyMotor neuronNerve netCalcium imagingGeneticsMedicineGeneCalciumInternal medicineSpinal cordNeurobiology and Insect Physiology ResearchDevelopmental Biology and Gene RegulationRetinal Development and Disorders
Temporal transcription factors determine circuit membership by permanently altering motor neuron-to-muscle synaptic partnerships | Litcius