Abstract

Sensory axons projecting to the central nervous system are organized into topographic maps that represent the locations of sensory stimuli. In some sensory systems, even adjacent sensory axons are arranged topographically, forming "fine-scale" topographic maps. Although several broad molecular gradients are known to instruct coarse topography, we know little about the molecular signaling that regulates fine-scale topography at the level of two adjacent axons. Here, we provide evidence that trans-synaptic BMP signaling mediates local inter-neuronal communication to regulate fine-scale topography in the nociceptive system of Drosophila larvae. We first show that the topographic separation of the axon terminals of adjacent nociceptors requires their common postsynaptic target, the A08n neurons. This phenotype is recapitulated by knockdown of the BMP ligand, Dpp, in these neurons. In addition, removing the type-II BMP receptors or their effector (Mad transcription factor) in single nociceptors impairs the fine-scale topography, suggesting the contribution of BMP signaling originated from A08n. This signaling is likely mediated by phospho-Mad in the presynaptic terminals of nociceptors to ensure local inter-neuronal communication. Finally, reducing Dpp levels in A08n reduces the nociceptor-A08n synaptic contacts. Our data support that trans-synaptic BMP signaling establishes the fine-scale topography by facilitating the formation of topographically correct synapses. Local BMP signaling for synapse formation may be a developmental strategy that independently regulates neighboring axon terminals for fine-scale topography.Significance Statement Sensory axons projecting to the central nervous system (CNS) are organized spatially to represent the locations of sensory stimuli. This occurs even between adjacent sensory axons. While much has been learned about the rough spatial arrangement of sensory axons in the CNS, the molecular signaling that arranges two adjacent axons remains poorly understood. The present study shows that this process is regulated by local inter-neuronal communication via a trans-synaptic BMP signaling that facilitates the synapse formation of the sensory axons that are appropriately located.

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