Tissue-specific and neural activity-regulated expression of human BDNF gene in BAC transgenic mice

被引:30
|
作者
Koppel, Indrek [1 ]
Aid-Pavlidis, Tamara [1 ]
Jaanson, Kaur [1 ]
Sepp, Mari [1 ]
Pruunsild, Priit [1 ]
Palm, Kaia [1 ]
Timmusk, Tonis [1 ]
机构
[1] Tallinn Univ Technol, Dept Gene Technol, EE-12618 Tallinn, Estonia
来源
BMC NEUROSCIENCE | 2009年 / 10卷
基金
英国惠康基金;
关键词
GREEN FLUORESCENT PROTEIN; NERVE GROWTH-FACTOR; NEUROTROPHIC FACTOR; RAT-BRAIN; MESSENGER-RNA; NEURONAL-ACTIVITY; CHOLINERGIC NEURONS; MULTIPLE PROMOTERS; CALCIUM REGULATION; MOLECULAR-CLONING;
D O I
10.1186/1471-2202-10-68
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Brain-derived neurotrophic factor (BDNF) is a small secreted protein that has important roles in the developing and adult nervous system. Altered expression or changes in the regulation of the BDNF gene have been implicated in a variety of human nervous system disorders. Although regulation of the rodent BDNF gene has been extensively investigated, in vivo studies regarding the human BDNF gene are largely limited to postmortem analysis. Bacterial artificial chromosome (BAC) transgenic mice harboring the human BDNF gene and its regulatory flanking sequences constitute a useful tool for studying human BDNF gene regulation and for identification of therapeutic compounds modulating BDNF expression. Results: In this study we have generated and analyzed BAC transgenic mice carrying 168 kb of the human BDNF locus modified such that BDNF coding sequence was replaced with the sequence of a fusion protein consisting of N-terminal BDNF and the enhanced green fluorescent protein (EGFP). The human BDNF-BAC construct containing all BDNF 5' exons preceded by different promoters recapitulated the expression of endogenous BDNF mRNA in the brain and several non-neural tissues of transgenic mice. All different 5' exon-specific BDNF-EGFP alternative transcripts were expressed from the transgenic human BDNF-BAC construct, resembling the expression of endogenous BDNF. Furthermore, BDNF-EGFP mRNA was induced upon treatment with kainic acid in a promotor-specific manner, similarly to that of the endogenous mouse BDNF mRNA. Conclusion: Genomic region covering 67 kb of human BDNF gene, 84 kb of upstream and 17 kb of downstream sequences is sufficient to drive tissue-specific and kainic acid-induced expression of the reporter gene in transgenic mice. The pattern of expression of the transgene is highly similar to BDNF gene expression in mouse and human. This is the first study to show that human BDNF gene is regulated by neural activity.
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页数:14
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