3.8 Article

The human tyrosine hydroxylase gene promoter

期刊

MOLECULAR BRAIN RESEARCH
卷 112, 期 1-2, 页码 8-23

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/S0169-328X(02)00694-0

关键词

human; tyrosine hydroxylase; brain; neurons; CNS; Parkinson's disease; stem cells; alcoholism; transplantation; transgenic mice; nurr1; NR4A2; bicoid; Gscl; goosecoid-like; HOXA4; HOXA5; GFP; EGFP; HNF-3beta; NRSE; neuron restrictive silencer element; development; Pitx3; promoter; transgene; neurons; dopaminergic neurons; dopamine; catecholamines; movement disorders; genetics

资金

  1. NINDS NIH HHS [R01 NS024204-13, R01 NS032519-12, NS24204, R01 NS032519-13, R01 NS032519-14, R01 NS024204-14, NS32519, R01 NS024204-12S1] Funding Source: Medline

向作者/读者索取更多资源

13.329 kilobases of the single copy human tyrosine hydroxylase (hTH) gene were isolated from a genomic library. The 5' flanking 11 kilobases fused to the reporter green fluorescent protein (GFP) drove high level expression in TH+ cells of the substantia nigra of embryonic and adult transgenic mice as determined by double label fluorescence microscopy. To provide a basis for future analysis of polymorphisms and structure-function studies, the previously unreported distal 10.5 kilobases of the hTH promoter were sequenced with an average coverage of 20-fold, the remainder with 4-fold coverage. Sequence features identified included four perfect matches to the bicoid binding element (BBE, consensus: BBTAATCYV) all of which exhibited specific binding by electrophoretic mobility shift assay (EMSA). Comparison to published sequences of mouse and rat TH promoters revealed five areas of exceptional homology shared by these species in the upstream TH promoter region -2 kb to -9 kb relative to the transcription start site. Within these conserved regions (CRs I-V), potential recognition sites for NR4A2 (Nurr1), HNF-3beta, HOXA4, and HOXA5 were shared across human, mouse, and rat TH promoters. (C) 2002 Published by Elsevier Science B.V.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

3.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据