The precise recognition of appropriate synaptic partner neurons is a critical step during neural circuit assembly. However, little is known about the developmental context in which recognition specificity is important to establish synaptic contacts. We show that in the Drosophila visual system, sequential segregation of photoreceptor afferents, reflecting their birth order, lead to differential positioning of their growth cones in the early target region. By combining loss- and gain-of-function analyses we demonstrate that relative differences in the expression of the transcription factor Sequoia regulate R cell growth cone segregation. This initial growth cone positioning is consolidated via cell-adhesion molecule Capricious in R8 axons. Further, we show that the initial growth cone positioning determines synaptic layer selection through proximity-based axon-target interactions. Taken together, we demonstrate that birth order dependent pre-patterning of afferent growth cones is an essential pre-requisite for the identification of synaptic partner neurons during visual map formation in Drosophila.
A nervous system requires a precise network of connections between cells called neurons to work properly. Within the brain, the fiber-like connections between pairs of neurons are not running crisscross like a pile of spaghetti. Instead, connected partner neurons are organized into distinct layers and columns.
Many questions remain about how these partner neurons find each other and how the layers of fiber-like connections form. To answer these questions, scientists often study the part of the fruit fly nervous system that controls the insect’s vision. This brain-like structure is simple and can be easily manipulated with genetic engineering. Fruit fly studies have helped identify some molecules that play a role in helping partner cells find one another and connect. These studies have also shown that the timing of brain cell development appears to play a role. But the role that layer formation plays in the process is still a mystery.
Now, Kulkarni et al. show that the birthdate of neurons in the fruit fly visual system helps organize them into layers. These neurons are generated early in the development of the fly. Shortly after birth, a molecular clock under the control of a protein called Sequoia starts within each newly generated neuron. The Sequoia protein is a transcription factor and controls the activity of many genes, and the molecular clock provides the growing neuron fibers with information about where and when to look for its partner neurons.
By manipulating the amount and time that Sequoia is produced in the fly visual system, Kulkarni et al. show that this clock helps arrange the growing cells into layers. Cells with similar birthdates connect and are arranged into layers. How much and when Sequoia is produced dictates where each new layer begins. The next steps for the research will be to learn more about how the clock works and identify any intermediaries between the clock and cell growth patterns.
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