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HT Experiment :

Experiment Id  GSE217297 Name  Transcriptional control of motor pool formation and motor circuit connectivity by the LIM-HD protein Isl2
Experiment Type  RNA-Seq Study Type  WT vs. Mutant
Source  GEO Curation Date  2024-06-25
description  The fidelity of motor control requires the precise positional arrangement of motor pools and the establishment of synaptic connections between these pools. In the developing spinal cord, motor nerves project to specific target muscles and receive proprioceptive input from the muscles via the sensorimotor circuit. LIM-homeodomain transcription factors are known to successively restrict specific motor neuronal fates during neural development; however, it remains unclear to what extent they contribute to limb-based motor pools and locomotor circuits. Here, we showed in mice that deletion of Isl2 resulted in scattered motor pools, primarily in the median motor column and lateral LMC (LMCl) populations, and lacked Pea3 expression in the hindlimb motor pools, accompanied by reduced terminal axon branching and disorganized neuromuscular junctions. Transcriptomic analysis of Isl2-deficient spinal cords revealed that a variety of genes involved in motor neuron differentiation, axon development, and synapse organization were downregulated in hindlimb motor pools. Moreover, the loss of Isl2 impaired sensorimotor connectivity and hindlimb locomotion. Together, our studies indicate that Isl2 plays a critical role in organizing motor pool position and sensorimotor circuits in hindlimb motor pools. RNA-seq of the ventral brachial and lumbar spinal cords, E12.5 embryonic spinal cords (from 3 animals of Isl2+/- and 3 animals of Isl2 KO). Ventral spinal cords were harvested and trimmed around the Hb9::GFP reporter.
  • variables:
  • anatomical structure,
  • genotype,
  • bulk RNA-seq

1 Publications

Trail: HTExperiment

12 Samples

Trail: HTExperiment