Gamma-aminobutryic acid (GABA) is the principal inhibitory neurotransmitter in both vertebrate and invertebrate nervous systems. GABA transporters largely mediate termination of GABA-stimulated inhibitory responses by the selective reuptake of GABA from the synaptic cleft. In this physiological context, efficient GABA transport mechanisms ensure the fidelity of neurotransmission. In addition, diversity in the mammalian GABA transporter isoforms is believed to regulate different aspects of GABAergic neurotransmission; preliminary work suggests the same is true for Drosophila. We cloned several partial GABA transporter-homologous cDNAs from a Drosophila head library that displayed extensive sequence homology with mammalian GABA transporters. The existence of experimentally accessible GABA transporters in Drosophila (DGATs) facilitates undertaking a molecular- genetic approach to better understand the neurochemical actions of GABA on behaviors. We hypothesize that alterations in GABA-mediated neurotransmission via perturbations in DGAT function will result in aberrant behaviors. We also hypothesize that different members of the DGAT family regulate different aspects of GABA-mediated behaviors. To verify these hypotheses, we will address three specific aims: 1) We will analyze pharmacologically induced behaviors In the adult fly that result from perturbations in GABA transporter function and GABA- mediated neurotransmission. 2) We will identify distinct members of the Drosophila GABA transporter family (DGATs) and functionally characterize the proteins by expressing them in Insect cells. 3) We will analyze the behavioral phenotypes of mutant strains of flies with abnormal GABA transporter expression. The proposed work will extend our knowledge of basic regulatory mechanisms governing GABA-mediated neurotransmission.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
3F32GM063491-02S1
Application #
6707156
Study Section
Biological Sciences 2 (BIOL)
Program Officer
Tompkins, Laurie
Project Start
2001-09-01
Project End
2003-08-31
Budget Start
2003-03-01
Budget End
2003-08-31
Support Year
2
Fiscal Year
2003
Total Cost
$23,210
Indirect Cost
Name
Saint Louis University
Department
Pharmacology
Type
Schools of Medicine
DUNS #
050220722
City
Saint Louis
State
MO
Country
United States
Zip Code
63103