Disturbed daily rhythms have been implicated in a variety of brain disorders. These rhythms are regulated by at least two intertwined pathways, one is the circadian clock and a second is the masking pathway that mediates activity in response to light. This proposal addresses these pathways using the fruit fly, Drosophila melanogaster. The genetic basis of circadian and masking function appears conserved, suggesting that findings in the fly will be widely applicable. A critical role for an enigmatic and highly conserved ion channel narrow abdomen (na) has been identified in both circadian output and masking regulation. These observations underlie the overall goal of this proposal, which is to provide an integrated view of na function in both masking and circadian rhythms at the behavioral, neuronal, and molecular levels.
The specific aims of this proposal are: 1. To map the neural substrates of na function. NA may function in circadian pacemaker neurons to regulate masking behavior. Tissue-specific rescue and assessments of NA distribution will be performed to address NA function in circadian and photoreceptor neurons. The regulation of NA by the clock and/or light will also be examined. 2. To define the electrophysiological phenotype of na mutant neurons. A method has been developed to examine the electrical properties of Drosophila pacemaker neurons. Characterization of ionic currents in these key neurons, the effects of na on these currents, as well as the electrophysiological properties of the elusive NA channel itself will be examined, including regulation by the circadian clock and/or light. 3. To assess the consequences of altered NA channel properties. NA is a unique and conserved member of the voltage-gated cation channel family. NA reveals many signatures of ion channels including highly conserved pore selectivity and voltage sensor sequences. The function of NA channels with altered pore or voltage sensor sequences will be tested by behavioral rescue. In total, these studies will define the electrophysiological function of NA within distinct anatomic pathways relevant to circadian and masking regulation. Given the conservation of clocks and NA, this proposal should illuminate human daily rhythms and their contribution to disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
1R01NS052903-01A1
Application #
6969516
Study Section
Special Emphasis Panel (ZRG1-BRS (01))
Program Officer
Mitler, Merrill
Project Start
2005-09-01
Project End
2009-08-31
Budget Start
2005-09-01
Budget End
2006-08-31
Support Year
1
Fiscal Year
2005
Total Cost
$343,406
Indirect Cost
Name
Northwestern University at Chicago
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
160079455
City
Evanston
State
IL
Country
United States
Zip Code
60201
Flourakis, Matthieu; Allada, Ravi (2015) Patch-clamp electrophysiology in Drosophila circadian pacemaker neurons. Methods Enzymol 552:23-44
Flourakis, Matthieu; Kula-Eversole, Elzbieta; Hutchison, Alan L et al. (2015) A Conserved Bicycle Model for Circadian Clock Control of Membrane Excitability. Cell 162:836-48
Lear, Bridget C; Darrah, Eric J; Aldrich, Benjamin T et al. (2013) UNC79 and UNC80, putative auxiliary subunits of the NARROW ABDOMEN ion channel, are indispensable for robust circadian locomotor rhythms in Drosophila. PLoS One 8:e78147
Lim, Chunghun; Lee, Jongbin; Choi, Changtaek et al. (2011) The novel gene twenty-four defines a critical translational step in the Drosophila clock. Nature 470:399-403
Allada, Ravi; Chung, Brian Y (2010) Circadian organization of behavior and physiology in Drosophila. Annu Rev Physiol 72:605-24
Zhang, Luoying; Chung, Brian Y; Lear, Bridget C et al. (2010) DN1(p) circadian neurons coordinate acute light and PDF inputs to produce robust daily behavior in Drosophila. Curr Biol 20:591-9
Kilman, Valerie L; Zhang, Luoying; Meissner, Rose-Anne et al. (2009) Perturbing dynamin reveals potent effects on the Drosophila circadian clock. PLoS One 4:e5235
Zhang, Luoying; Lear, Bridget C; Seluzicki, Adam et al. (2009) The CRYPTOCHROME photoreceptor gates PDF neuropeptide signaling to set circadian network hierarchy in Drosophila. Curr Biol 19:2050-5
Kilman, Valerie L; Allada, Ravi (2009) Genetic analysis of ectopic circadian clock induction in Drosophila. J Biol Rhythms 24:368-78
Chung, Brian Y; Kilman, Valerie L; Keath, J Russel et al. (2009) The GABA(A) receptor RDL acts in peptidergic PDF neurons to promote sleep in Drosophila. Curr Biol 19:386-90

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