We all have memories and we all know that we forget some of the crucial ones - especially as we grow older. Our long-term objective is to understand how a brain encodes memory at the molecular and cellular level. We use the fruit fly Drosophila as our model system because it can learn, it has a relatively simple brain and it is amenable to a genetic approach. This application focuses on the Drosophila amnesiac (amn) mutant. Mutant amn flies have poor memory. The amn gene encodes a putative preproneuropeptide with homology to the mammalian neuromodulator pituitary adenylyl cyclase activating peptide (PACAP). We will take molecular genetic and behavioral approaches to understand the role of amn in memory.
Our specific aims are: 1. Identify the AMN neuropeptide fragment(s) that are required for memory. Are all the putative fragments of the precursor required for memory and if not, which ones are? Is the PACAP homology important? 2, Identify the memory-relevant AMN receptor(s). Are the predicted fly PACAP-type receptors involved in memory? Are they the AMN receptor(s)? 3. Delineate the intracellular signaling cascade affected by AMN. We have a mutant in a new potential component of PACAP signaling - a receptor tyrosine kinase, off-track. We will analyze the involvement of off-track in learning and more specifically, in AMN signaling. The genes involved in Drosophila learning have related mammalian genes that function similarly. Furthermore, it is becoming increasingly clear that learning-like synaptic plasticity is engaged- in the relevant neural circuits - by drugs of human abuse. Therefore molecules we identify in Drosophila learning may ultimately be useful in human mnemonic and drug rehabilitation therapy.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH069883-05
Application #
7323313
Study Section
Integrative, Functional and Cognitive Neuroscience 8 (IFCN)
Program Officer
Beckel-Mitchener, Andrea C
Project Start
2003-12-01
Project End
2009-06-19
Budget Start
2007-12-01
Budget End
2009-06-19
Support Year
5
Fiscal Year
2008
Total Cost
$305,291
Indirect Cost
Name
University of Massachusetts Medical School Worcester
Department
Biology
Type
Schools of Medicine
DUNS #
603847393
City
Worcester
State
MA
Country
United States
Zip Code
01655
Perrat, Paola N; DasGupta, Shamik; Wang, Jie et al. (2013) Transposition-driven genomic heterogeneity in the Drosophila brain. Science 340:91-5
Burke, Christopher J; Huetteroth, Wolf; Owald, David et al. (2012) Layered reward signalling through octopamine and dopamine in Drosophila. Nature 492:433-7
Perisse, Emmanuel; Waddell, Scott (2011) Associative memory: without a trace. Curr Biol 21:R579-81
Huetteroth, Wolf; Waddell, Scott (2011) Bringing fly brains in line. Nat Methods 8:461-3
Pitman, Jena L; Huetteroth, Wolf; Burke, Christopher J et al. (2011) A pair of inhibitory neurons are required to sustain labile memory in the Drosophila mushroom body. Curr Biol 21:855-61
Huetteroth, Wolf; Waddell, Scott (2011) Hungry flies tune to vinegar. Cell 145:17-8
Burke, Christopher J; Waddell, Scott (2011) Remembering nutrient quality of sugar in Drosophila. Curr Biol 21:746-50
Krashes, Michael J; Waddell, Scott (2011) Drosophila appetitive olfactory conditioning. Cold Spring Harb Protoc 2011:pdb.prot5609
Krashes, Michael J; Waddell, Scott (2011) Drosophila aversive olfactory conditioning. Cold Spring Harb Protoc 2011:pdb.prot5608
Koon, Alex C; Ashley, James; Barria, Romina et al. (2011) Autoregulatory and paracrine control of synaptic and behavioral plasticity by octopaminergic signaling. Nat Neurosci 14:190-9

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