The macromolecules comprising neural structures are constructed and assembled according to genetic information. Our objective is to study how genes control the structure and function of the nervous system. Behavioral mutants are isolated in Drosophila melanogaster including those that are conditional paralytic mutants. These are characterized beaviorally and genetically. Intracellular recordings are performed on larval muscle to identify and analyze those mutants with defects in nerve conduction, neuromuscular transmission, or muscle response. Among those mutants that we have been studying are those that block the propagation of action potential (e.g. nap ts, para ts) and those that cause repetitive firing of action potentials (e.g., Sh, bas MW1). Functional relationships among the various gene products comprising neuronal membranes are studied by examining epistatic and suppressive interactions in double mutants. Isolation of additonal mutants is being carried out to further extend our spectrum of genetic modifications of membrane excitability. This analysis establishes a framework for the eventual identification of the molecular components of the nervous system and may provide a better understanding of the underlying defect in certain heritable neurological disorders in humans.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS015390-07
Application #
3396199
Study Section
Genetics Study Section (GEN)
Project Start
1979-07-01
Project End
1987-06-30
Budget Start
1985-07-01
Budget End
1986-06-30
Support Year
7
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
Earth Sciences/Resources
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Cunningham, Patrick C; Waldeck, Katherine; Ganetzky, Barry et al. (2018) Neurodegeneration and locomotor dysfunction in Drosophila scarlet mutants. J Cell Sci 131:
Babcock, Daniel T; Shen, Wei; Ganetzky, Barry (2015) A neuroprotective function of NSF1 sustains autophagy and lysosomal trafficking in Drosophila. Genetics 199:511-22
Babcock, Daniel T; Ganetzky, Barry (2015) Transcellular spreading of huntingtin aggregates in the Drosophila brain. Proc Natl Acad Sci U S A 112:E5427-33
Babcock, Daniel T; Ganetzky, Barry (2015) Non-cell autonomous cell death caused by transmission of Huntingtin aggregates in Drosophila. Fly (Austin) 9:107-9
Ballard, Shannon L; Miller, Daniel L; Ganetzky, Barry (2014) Retrograde neurotrophin signaling through Tollo regulates synaptic growth in Drosophila. J Cell Biol 204:1157-72
Coyle, Ian P (2014) Confocal imaging of fluorescently labeled proteins in the Drosophila larval neuromuscular junction. Methods Mol Biol 1075:201-12
Campbell, Megan; Ganetzky, Barry (2013) Identification of Mob2, a novel regulator of larval neuromuscular junction morphology, in natural populations of Drosophila melanogaster. Genetics 195:915-26
Miller, Daniel L; Ballard, Shannon L; Ganetzky, Barry (2012) Analysis of synaptic growth and function in Drosophila with an extended larval stage. J Neurosci 32:13776-86
Chen, Xu; Ganetzky, Barry (2012) A neuropeptide signaling pathway regulates synaptic growth in Drosophila. J Cell Biol 196:529-43
Chen, Xu; Peterson, Jonathan; Nachman, Ronald J et al. (2012) Drosulfakinin activates CCKLR-17D1 and promotes larval locomotion and escape response in Drosophila. Fly (Austin) 6:290-7

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