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

被引:36
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
收藏
页码:269 / 277
页数:9
相关论文
共 32 条
[1]   The transcriptional regulator Yin Yang 1 activates the myelin PLP gene [J].
Berndt, JA ;
Kim, JG ;
Tosic, M ;
Kim, C ;
Hudson, LD .
JOURNAL OF NEUROCHEMISTRY, 2001, 77 (03) :935-942
[2]   The neuron-restrictive silencer element: A dual enhancer/silencer crucial for patterned expression of a nicotinic receptor gene in the brain [J].
Bessis, A ;
Champtiaux, N ;
Chatelin, L ;
Changeux, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (11) :5906-5911
[3]   DIFFERENTIAL EXPRESSION OF 2 NEURAL CELL-SPECIFIC BETA-TUBULIN MESSENGER-RNAS DURING RAT-BRAIN DEVELOPMENT [J].
BOND, JF ;
ROBINSON, GS ;
FARMER, SR .
MOLECULAR AND CELLULAR BIOLOGY, 1984, 4 (07) :1313-1319
[4]   STRUCTURE AND TRANSCRIPTIONAL REGULATION OF THE GFAP GENE [J].
BRENNER, M .
BRAIN PATHOLOGY, 1994, 4 (03) :245-257
[5]   The GAP-43 gene is a direct downstream target of the basic helix-loop-helix transcription factors [J].
Chiaramello, A ;
Neuman, T ;
Peavy, DR ;
Zuber, MX .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (36) :22035-22043
[6]  
CLEVELAND DW, 1985, ANNU REV BIOCHEM, V54, P331, DOI 10.1146/annurev.bi.54.070185.001555
[7]  
EASTER SS, 1993, J NEUROSCI, V13, P285
[8]  
GLOSTER A, 1994, J NEUROSCI, V14, P7319
[9]  
Katsetos CD, 2001, ARCH PATHOL LAB MED, V125, P613
[10]   Related enhancers in the intron of the beta 1 tubulin gene of Drosophila melanogaster are essential for maternal and CNS-specific expression during embryogenesis [J].
Kohler, J ;
SchaferPreuss, S ;
Buttgereit, D .
NUCLEIC ACIDS RESEARCH, 1996, 24 (13) :2543-2550