Melinda Kehribar, Charlotte B. Wit, Ksenia Krasikova, Egemen Agi, Eric T. Reifenstein, Neele Wolterhoff, Lasse Q. Wriedt, Max von Kleist, P. Robin Hiesinger
Flies, like vertebrates, preserve the spatial organization of visual input through axonal projections into the brain, a principle called retinotopy. The best-known developmental mechanisms for retinotopy are molecular gradients in the target regions, yet Drosophila photoreceptors can form retinotopic maps ectopically in wrong brain regions. We show that a temporal gradient of axonal growth plus selective adhesion between photoreceptor axons precisely preserves the cellular eye pattern. Each of the 800 single eyes, the ommatidia, form a bundle of six axons that are held in place by inter-bundle adhesion through the protocadherin Flamingo and preserve their intra-bundle organization through the adhesion molecule Sidekick. Computational modeling of axon terminals as selectively adhesive soft bodies in a developmental wave generates the retinotopic pattern, including the shapes of the postsynaptic lamina neurons, which emerge without explicit encoding. Hence, a temporal gradient and two adhesive forces can ensure retinotopic map formation without a target-derived mechanism. VIDEO ABSTRACT.