Cloning and characterization of the 5′-flanking region of the rat neuron-specific Class III β-tubulin gene

被引:34
作者
Dennis, K [1 ]
Uittenbogaard, M [1 ]
Chiaramello, A [1 ]
Moody, SA [1 ]
机构
[1] George Washington Univ, Inst Biomed Sci, Program Neurosci, Dept Anat & Cell Biol, Washington, DC 20037 USA
关键词
neuronal differentiation; promoter; E-box; GTTTT repeat; SP1 transcription factor; gene expression;
D O I
10.1016/S0378-1119(02)00801-6
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The promoter regions of several neuron-specific structural proteins (e.g. neurofilaments, peripherin, Talpha1-tubulin) have revealed potential regulatory elements that could contribute to the choice of a neuronal phenotype during development. We initiated study of the 5'-flanking region of the rat Class III neuron-specific beta-tubulin gene (betaIII-tubulin) because this gene is expressed at the time of terminal mitosis only in neurons and thus its promoter should be an excellent tool for studying neuron-specific gene expression during the transition from proliferative progenitor cell to early neuronal differentiation. We identified the minimal promoter region needed to drive expression of the betaIII-tubulin gene. This minimal region contains multiple putative binding sites for the transcription factors SP1 and AP2, as well as a central nervous system enhancer regulatory element and an E-box. A primer extension analysis identifies a single transcription start site. We highlight several putative regulatory elements that may modulate the expression of the betaIII-tubulin gene in a stage- and tissue-specific manner. In addition, we show that the first 490 bp of the promoter are sufficient to regulate betaIII-tubulin gene expression during neuronal differentiation of PCC7 cells. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
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页码:269 / 277
页数:9
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