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Dichotomous cis-regulatory motifs mediate the maturation of the neuromuscular junction by retrograde BMP signaling.

Robin VuilleumierMo MiaoSonia Medina-GiroClara-Maria EllStephane FlibotteTianshun LianGrant KauweAnnie CollinsSophia LyGeorge PyrowolakisA Pejmun HaghighiDouglas W Allan
Published in: Nucleic acids research (2022)
Retrograde bone morphogenetic protein (BMP) signaling at the Drosophila neuromuscular junction (NMJ) has served as a paradigm to study TGF-β-dependent synaptic function and maturation. Yet, how retrograde BMP signaling transcriptionally regulates these functions remains unresolved. Here, we uncover a gene network, enriched for neurotransmission-related genes, that is controlled by retrograde BMP signaling in motor neurons through two Smad-binding cis-regulatory motifs, the BMP-activating (BMP-AE) and silencer (BMP-SE) elements. Unpredictably, both motifs mediate direct gene activation, with no involvement of the BMP derepression pathway regulators Schnurri and Brinker. Genome editing of candidate BMP-SE and BMP-AE within the locus of the active zone gene bruchpilot, and a novel Ly6 gene witty, demonstrated the role of these motifs in upregulating genes required for the maturation of pre- and post-synaptic NMJ compartments. Our findings uncover how Smad-dependent transcriptional mechanisms specific to motor neurons directly orchestrate a gene network required for synaptic maturation by retrograde BMP signaling.
Keyphrases
  • mesenchymal stem cells
  • bone regeneration
  • genome wide
  • genome wide identification
  • copy number
  • transcription factor
  • genome editing
  • transforming growth factor
  • spinal cord injury
  • prefrontal cortex