The long term goal of this project is to define basic molecular mechanisms that underlie circadian rhythms of behavior in vertebrates. A wide variety of biochemical and physiological processes are regulated by circadian clocks, resulting in coordinated daily rhythms of gene expression, metabolism, neurochemical and hormonal functions, and behavior. Disruption of the human circadian system due to disease, aging or voluntary disruption of sleep-wake cycles can lead to diminished sensory and motor performance, sleep disorders or affective disorders. An understanding of the biological basis of circadian rhythmicity will be important for undertanding and treatment of these disorders. The specific goal of this project is to identify and characterize vertebrate genes that are involved in circadian rhythmicity through mutational analysis of the zebrafish circadian system. Recent advances in zebrafish genetics and genomics, together with recently-developed methods for efficient measurement of zebrafish circadian rhythms, make this a useful and economical model system for genetic studies of vertebrate circadian clocks.
The specific aims of this project are to: 1) Screen for mutations that affect behavioral circadian rhythms in matugenized zebrafish, recover mutant lines, and characterize the phenotypes of these mutations at the system and cellular levels. 2) Map these mutations on the zebrafish genetic linkage map. 3) Clone and map zebrafish homologs of known circadian clock-related genes and determine whether any of these are disrupted by the newly identified mutations. 4) Use candidate and positional cloning techniques to clone mutated clock genes. This project is expected to result in the identification of novel vertebrate circadian clock genes, and in new information about the functional roles and mechanisms of action of previously- identified clock-related genes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH060939-03
Application #
6490865
Study Section
Special Emphasis Panel (ZRG1-MDCN-6 (01))
Program Officer
Brady, Linda S
Project Start
2000-01-01
Project End
2003-12-31
Budget Start
2002-01-01
Budget End
2002-12-31
Support Year
3
Fiscal Year
2002
Total Cost
$190,738
Indirect Cost
Name
University of Houston
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
800771594
City
Houston
State
TX
Country
United States
Zip Code
77204
Tan, Ying; DeBruyne, Jason; Cahill, Gregory M et al. (2008) Identification of a mutation in the Clock1 gene affecting zebrafish circadian rhythms. J Neurogenet 22:149-66
Rawashdeh, Oliver; de Borsetti, Nancy Hernandez; Roman, Gregg et al. (2007) Melatonin suppresses nighttime memory formation in zebrafish. Science 318:1144-6
Kaneko, Maki; Hernandez-Borsetti, Nancy; Cahill, Gregory M (2006) Diversity of zebrafish peripheral oscillators revealed by luciferase reporting. Proc Natl Acad Sci U S A 103:14614-9
Kaneko, Maki; Cahill, Gregory M (2005) Light-dependent development of circadian gene expression in transgenic zebrafish. PLoS Biol 3:e34
DeBruyne, Jason; Hurd, Mark W; Gutierrez, Laura et al. (2004) Isolation and phenogenetics of a novel circadian rhythm mutant in zebrafish. J Neurogenet 18:403-28
Cermakian, Nicolas; Pando, Matthew P; Thompson, Carol L et al. (2002) Light induction of a vertebrate clock gene involves signaling through blue-light receptors and MAP kinases. Curr Biol 12:844-8