Human and mouse dopamine transporter genes: conservation of 5'-flanking sequence elements and gene structures.

Article Details

Citation

Donovan DM, Vandenbergh DJ, Perry MP, Bird GS, Ingersoll R, Nanthakumar E, Uhl GR

Human and mouse dopamine transporter genes: conservation of 5'-flanking sequence elements and gene structures.

Brain Res Mol Brain Res. 1995 Jun;30(2):327-35.

PubMed ID
7637582 [ View in PubMed
]
Abstract

Synaptic reaccumulation of the neurotransmitter dopamine is mediated by the dopamine transporter (DAT), a member of the family of twelve transmembrane domain, sodium- and chloride-dependent neurotransmitter transporters. Several DAT features, including its exclusive expression in dopaminergic neurons, implication in cocaine action, and prominent role in the mechanisms of Parkinsonism-inducing neurotoxins, make understanding of the DAT gene of interest. Isolation and characterization of the human and mouse DAT genes has allowed elucidation of similarities between each and other members of this transporter gene family. Sequences 5' to transcriptional start sites contain G-C rich, TATA-less, CAAT-less regions with striking conservation between human and mouse gene flanking regions. These studies suggest sequence elements that are candidates to contribute to the dopamine transporter's dopaminergic cell-specific expression.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Sodium-dependent dopamine transporterQ01959Details
Sodium-dependent dopamine transporterQ61327Details