Control of synaptic specificity by limiting promiscuous synapse formation

Xu, C.; Theisen, E.; Rumbaut, E.; Shum, B.; Peng, J.; Tarnogorska, D.; Borycz, J. A.; Tan, L.; Courgeon, M.; Meinertzhagen, I. A.; Pecot, M. Y.

doi:10.1101/415695

bioRxiv · 10.1101/415695

Control of synaptic specificity by limiting promiscuous synapse formation

Xu, C.·Theisen, E.·Rumbaut, E.·Shum, B.·Peng, J.·Tarnogorska, D.·Borycz, J. A.·Tan, L.·Courgeon, M.·Meinertzhagen, I. A.·Pecot, M. Y.

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Abstract

The ability of neurons to distinguish appropriate from inappropriate synaptic partners in their local environment is fundamental to the proper assembly and function of neural circuits. How synaptic partner selection is regulated is a longstanding question in Neurobiology. A prevailing hypothesis is that appropriate partners express complementary molecules that match them together and promote synaptogenesis. Dpr and DIP IgSF proteins bind heterophilically and are expressed in a complementary manner between synaptic partners in the Drosophila visual system. Here, we show that in the lamina, DIP mis-expression is sufficient to promote synapse formation with Dpr-expressing neurons, and that DIP proteins are not necessary for synaptogenesis but rather function to prevent ectopic synapse formation. These findings indicate that Dpr-DIP interactions regulate synaptic specificity by biasing synapse formation towards specific cell-types. We propose that synaptogenesis occurs independent of synaptic partner choice, and that precise synaptic connectivity is established by limiting promiscuous synapse formation.

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Xu, C., Theisen, E., Rumbaut, E., Shum, B., Peng, J., Tarnogorska, D., Borycz, J. A., Tan, L., Courgeon, M., Meinertzhagen, I. A., Pecot, M. Y.. 2018-09-12. Control of synaptic specificity by limiting promiscuous synapse formation. https://doi.org/10.1101/415695

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