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Cloning and expression of a rat brain GABA transporter

Journal Article · · Science (Washington, D.C.); (USA)
; ; ;  [1]; ; ;  [2]; ;  [3]
  1. California Institute of Technology, Pasadena, CA (USA)
  2. Roche Institute of Molecular Biology, Nutley, NJ (USA)
  3. Hebrew Univ., Jerusalem (Israel)
A complementary DNA clone (designated GAT-1) encoding a transporter for the neurotransmitter {gamma}-aminobutyric acid (GABA) has been isolated from rat brain, and its functional properties have been examined in Xenopus oocytes. Oocytes injected with GAT-1 synthetic messenger RNA accumulated ({sup 3}H)GABA to levels above control values. The transporter encoded by GAT-1 has a high affinity for GABA, is sodium- and chloride-dependent, and is pharmacologically similar to neuronal GABA transporters. The GAT-1 protein shares antigenic determinants with a native rat brain GABA transporter. The nucleotide sequence of GAT-1 predicts a protein of 599 amino acids with a molecular weight of 67 kilodaltons. Hydropathy analysis of the deduced protein suggests multiple transmembrane regions, a feature shared by several cloned transporters; however, database searches indicate that GAT-1 is not homologous to any previously identified proteins. Therefore, GAT-1 appears to be a member of a previously uncharacterized family of transport molecules.
OSTI ID:
5763143
Journal Information:
Science (Washington, D.C.); (USA), Journal Name: Science (Washington, D.C.); (USA) Vol. 249:4974; ISSN SCIEA; ISSN 0036-8075
Country of Publication:
United States
Language:
English