Identification of an intronic cis-acting element in the human dopamine transporter gene

被引:10
|
作者
Zhao, Ying [1 ,2 ,3 ]
Zhou, Yanhong [1 ,2 ]
Xiong, Nian [1 ,2 ,4 ]
Lin, Zhicheng [1 ,2 ]
机构
[1] McLean Hosp, Div Alcohol & Drug Abuse, Belmont, MA 02478 USA
[2] Harvard Univ, Sch Med, Dept Psychiat, Boston, MA 02115 USA
[3] Xinxiang Med Univ, Sch Pharm, Xinxiang, Henan, Peoples R China
[4] Huazhong Univ Sci & Technol, Dept Neurol, Union Hosp, Tongji Med Coll, Wuhan 430074, Hubei, Peoples R China
基金
美国国家卫生研究院;
关键词
DAT; SLC6A3; Medication target; Promoter activity; Cell type-dependent; Primate-specific; TRANSCRIPTION FACTOR; REGIONAL DIFFERENCES; EXPRESSION; ACTIVATOR; PROMOTER; CONSUMPTION; REPRESSOR; SLC18A2; PROTEIN; MICE;
D O I
10.1007/s11033-011-1339-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The human dopamine transporter gene (hDAT) encodes the dopamine transporter in dopamine (DA) neurons to regulate DA transmission. hDAT expression varies significantly from neuron to neuron, and from individual to individual so that dysregulation of hDAT is related to many neuropsychiatric disorders. It is critical to identify hDAT-specific cis-acting elements that regulate the hDAT expression. Previous studies showed that hDAT Intron 1 displayed inhibitory activity for reporter gene expression. Here we report that the hDAT Intron 1 contains a 121-bp fragment that down-regulated both SV40 and hDAT promoter activities by 80% in vitro. Subfragments of 121-bp still down-regulated the SV40 promoter but not the hDAT promoter, as supported by nuclear protein-binding activities. Collectively, 121-bp is a silencer in vitro that might coordinate with transcriptional activities both inside and outside 121-bp in regulation of hDAT.
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页码:5393 / 5399
页数:7
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