Abstract
Converting sensory information into motor commands is fundamental to most of our actions1,2. In Drosophila, visuomotor transformations are mediated by Visual Projection Neurons (VPNs)3,4. These neurons convert object location and motion into directional behaviors downstream through a synaptic gradient mechanism5. However, the molecular origins of such graded connectivity remain unknown. We addressed this question in a VPN cell type called LPLC26, which integrates looming motion and transforms it into an escape response through two parallel dorsoventral synaptic gradients at its inputs and outputs. We identified two corresponding dorsoventral expression gradients of cell recognition molecules within the LPLC2 population that regulate this synaptic connectivity. Dpr13 determines synaptic outputs of LPLC2 axons by interacting with its binding partner DIP-ε expressed in the Giant Fiber, a neuron that mediates escape7. Similarly, beat-VI regulates synaptic inputs onto LPLC2 dendrites by interacting with Side-II expressed in upstream motion-detecting neurons. Behavioral, physiological, and molecular experiments demonstrate that these coordinated molecular gradients control differential synaptic connectivity, enabling the accurate transformation of visual features into motor commands. As within-neuronal-type continuous variation in gene expression is also observed in the mammalian brain8, graded expression of cell recognition molecules may represent a common mechanism underlying synaptic specificity.
Competing Interest Statement
The authors have declared no competing interest.
