Giros B, el Mestikawy S, Bertrand L, Caron M G
Department of Cell Biology, Duke University Medical Center, Durham, NC 27710.
FEBS Lett. 1991 Dec 16;295(1-3):149-54. doi: 10.1016/0014-5793(91)81406-x.
We report the cloning of a rat cDNA encoding a functional dopamine transporter. This cDNA, derived from an intron-containing gene, encodes a protein of 620 amino acids. Hydropathicity analysis of the protein sequence suggests the presence of 12 putative transmembrane domains. The protein displays considerable identity with transporters for noradrenaline and GABA (64 and 30%, respectively). Transient expression of the cDNA in COS7 cells directs the expression of dopamine uptake activity with appropriate pharmacology and in a sodium-dependent fashion. In situ hybridization reveals that the mRNA for this transporter is expressed in the substantia nigra and ventral tegmental area, regions that contain dopaminergic cell bodies.
我们报道了编码功能性多巴胺转运体的大鼠cDNA的克隆。该cDNA来源于一个含内含子的基因,编码一个由620个氨基酸组成的蛋白质。对该蛋白质序列的亲水性分析表明存在12个假定的跨膜结构域。该蛋白质与去甲肾上腺素和GABA转运体具有相当高的同源性(分别为64%和30%)。该cDNA在COS7细胞中的瞬时表达以适当的药理学特性和钠依赖性方式指导多巴胺摄取活性的表达。原位杂交显示该转运体的mRNA在黑质和腹侧被盖区表达,这些区域含有多巴胺能细胞体。