HUMAN AND MOUSE DOPAMINE TRANSPORTER GENES - CONSERVATION OF 5'-FLANKING SEQUENCE ELEMENTS AND GENE STRUCTURES

被引:64
作者
DONOVAN, DM
VANDENBERGH, DJ
PERRY, MP
BIRD, GS
INGERSOLL, R
NANTHAKUMAR, E
UHL, GR
机构
[1] MOLEC NEUROBIOL BRANCH, BALTIMORE, MD 21224 USA
[2] NIDA, ADDICT RES CTR, DIV INTRAMURAL RES, OFF DIRECTOR, BALTIMORE, MD 21224 USA
[3] GENET CORE FACIL, BALTIMORE, MD 21205 USA
[4] JOHNS HOPKINS UNIV, SCH MED, DEPT NEUROL, BALTIMORE, MD 21205 USA
[5] JOHNS HOPKINS UNIV, SCH MED, DEPT NEUROSCI, BALTIMORE, MD 21205 USA
来源
MOLECULAR BRAIN RESEARCH | 1995年 / 30卷 / 02期
关键词
TRANSPORTER; PROMOTER; GENE; PARKINSONS DISEASE; COCAINE;
D O I
10.1016/0169-328X(95)00018-N
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:327 / 335
页数:9
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