Muscle-selective RUNX3 dependence of sensorimotor circuit development

Development. 2019 Oct 24;146(20):dev181750. doi: 10.1242/dev.181750.

Abstract

The control of all our motor outputs requires constant monitoring by proprioceptive sensory neurons (PSNs) that convey continuous muscle sensory inputs to the spinal motor network. Yet the molecular programs that control the establishment of this sensorimotor circuit remain largely unknown. The transcription factor RUNX3 is essential for the early steps of PSNs differentiation, making it difficult to study its role during later aspects of PSNs specification. Here, we conditionally inactivate Runx3 in PSNs after peripheral innervation and identify that RUNX3 is necessary for maintenance of cell identity of only a subgroup of PSNs, without discernable cell death. RUNX3 also controls the sensorimotor connection between PSNs and motor neurons at limb level, with muscle-by-muscle variable sensitivities to the loss of Runx3 that correlate with levels of RUNX3 in PSNs. Finally, we find that muscles and neurotrophin 3 signaling are necessary for maintenance of RUNX3 expression in PSNs. Hence, a transcriptional regulator that is crucial for specifying a generic PSN type identity after neurogenesis is later regulated by target muscle-derived signals to contribute to the specialized aspects of the sensorimotor connection selectivity.

Keywords: Dorsal root ganglia; Neuronal specification; Neurotrophins; Sensorimotor circuit; Sensory system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / genetics
  • Cell Differentiation / physiology
  • Cells, Cultured
  • Core Binding Factor Alpha 3 Subunit / genetics
  • Core Binding Factor Alpha 3 Subunit / metabolism*
  • Female
  • Ganglia, Spinal / cytology
  • Ganglia, Spinal / metabolism
  • Gene Expression Regulation, Developmental
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / metabolism
  • LIM-Homeodomain Proteins / genetics
  • LIM-Homeodomain Proteins / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Microfilament Proteins / genetics
  • Microfilament Proteins / metabolism
  • Motor Neurons / metabolism
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism
  • Nerve Growth Factors / genetics
  • Nerve Growth Factors / metabolism
  • Sensory Receptor Cells / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • Avil protein, mouse
  • Core Binding Factor Alpha 3 Subunit
  • Homeodomain Proteins
  • Isl2 protein, mouse
  • LIM-Homeodomain Proteins
  • Lbx1h protein, mouse
  • Microfilament Proteins
  • Muscle Proteins
  • Nerve Growth Factors
  • Transcription Factors
  • Hb9 protein, mouse