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Investigating the molecular mechanisms that underlie tiling in Drosophila R7 photoreceptors Jennifer Salamé George Fox University
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Topographical maps: a major principle of organization in the nervous system cell body synapse These synapses do not overlap (i.e. are "tiled").
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Human retina is an example of a topographical map
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Fly R7 photoreceptors: a great model to study tiling
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Neuron circuit development occurs through two steps: axon pathfinding and synapse formation
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Synapse Formation 1. filopodia search 2. cell adhesion stabilizes 3. pre-synaptic components accumulate 4. post-synaptic assembly
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R7 axons require an Activin signal to tile Wild-type R7s imp 3 mutant R7s
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Test the hypothesis that excessive synapse formation causes the tiling defect
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Test the hypothesis that excessive synapse formation causes the tiling defect Excessive synapse formation Axon pathfinding error
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Necessary Approach 1: test whether synapse formation is necessary for the tiling defect
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Necessary Not necessary Approach 1: test whether synapse formation is necessary for the tiling defect
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Create syd-1, imp 3 R7s Wild type imp 3 mutant: tiling defect imp 3, syd-1 double mutant: ????? syd-1 mutant: cannot form synapses
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imp 3 syd-1 Test for non-complementation Create a syd-1, imp 3 double mutantchromosome syd-1 Bal x imp 3 Bal x imp 3 syd-1 Bal
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syd-1, imp 3 has a tiling defect
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Approach 2: test whether excessive synapse formation is sufficient to cause a tiling defect
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yes sufficient not sufficient
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C. elegans rsy-1 mutant neurons form excessive synapses
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Create drsy-1 mutant R7s in Drosophila FRT82drsy-1(Del) Bal x x drsy-1(Del) FRT82 Bal FRT82drsy-1(Del) Bal Test with PCR and eye color FRT82 Positive Control Candidates Bal
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drsy-1 mutants do not have a tiling defect
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Effect on synapse formation of drsy-1 mutation is inconclusive
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Conclusions Synapse formation is not necessary for a tiling defect Excessive synapse formation may not be sufficient to cause a tiling defect Disrupting Activin pathway seems to affect axon pathfinding Axon pathfinding error
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Future Research Directions Quantify synapses in drsy-1 mutants Quantify synapses in tiling defect mutants Identify genes regulated by Activin pathway in R7s
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Acknowledgments UO Institute of Molecular Biology Dr. Tory Herman Jennifer Jeffress Erik Lyons Jon Kniss Scott Holbrook University of Oregon SPUR Program Dr. Peter O’Day Chelsie Fish Other SPUR Interns!
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