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GABA transporters inDrosophila melanogaster: molecular cloning, behavior, and physiology

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Invertebrate Neuroscience

Abstract

Molecular cloning of GABA transporter-homologous cDNAs from aDrosophila melanogaster headspecific library was accomplished using a conserved oligomer from a highly conserved domain within the mammalian GABA transporters. Partial DNA sequencing of these cDNAs demonstrated homology with the mammalian transporters, indicating these are ancient, evolutionarily conserved molecules. Although theDrosophila cDNAs had distinct restriction enzyme patterns, they recognized the same locus inDrosophila genomic DNA, suggesting that the multiple isoforms might arise via alternative splicing. Antibodies specific for the mammalian GABA transporters GAT1, GAT2 and GAT3 recognized non-overlapping and developmentally distinct patterns of expression inDrosophila neuronal tissues. Treatment of larval instars with nipecotic acid, a generalized GABA reuptake inhibitor, revealed specific, dose-dependent alterations in behavior consistent with the presence of multiple transporter molecules with differing affinities for this drug. Synaptic current recordings revealed that nipecotic acid treated larvae have an increase in latency jitter of evoked quantal release, resulting in a broader average excitatory junctional current which was manifested in a broader EJP. These results imply that alterations in the development of the CNS occur if GABAergic neurotransmission is protentiated during development. The data suggest that, as in mammals, there are multiple GABA transporters inDrosophila whose expression is differentially regulated.

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Authors and Affiliations

  1. Department of Pharmacology and Physiological Sciences, St. Louis University School of Medicine, 63104, St Louis, MO, USA

    W. S. Neckameyer & R. L. Cooper

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  1. W. S. Neckameyer
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  2. R. L. Cooper
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Correspondence to W. S. Neckameyer.

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Neckameyer, W.S., Cooper, R.L. GABA transporters inDrosophila melanogaster: molecular cloning, behavior, and physiology. Invertebrate Neuroscience 3, 279–294 (1998). https://doi.org/10.1007/BF02577688

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