Promoter analysis of the Drosophila genes encoding TFIIB and TATA box-binding protein

被引:0
|
作者
Cho, N
Oh, Y
Hwang, SY
Han, D
Park, SP
Yoon, J
Han, K
Baek, K [1 ]
机构
[1] Kyung Hee Univ, Dept Genet Engn, Yongin City 449701, South Korea
[2] Kyung Hee Univ, Inst Genet Engn, Yongin City 449701, South Korea
[3] Taejon Univ, Dept Microbiol, Taejon 300716, South Korea
[4] Hallym Univ, Dept Genet Engn, Chunchon 200702, South Korea
关键词
Drosophila; promoter analysis; TBP; TFIIB;
D O I
暂无
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
We have analyzed the 5'-flanking regions of the Drosophila genes encoding the TFIIB and TATA box-binding proteins (TBP) and mapped the regulatory regions required for their efficient expression. We found that the 500 bp long region (-439 to +60) and the 401 bp long region (-261 to +138) are required for the efficient expression of TFIIB and TBP genes, respectively. In the TFIIB promoter region, the upstream DNA between -439 and -280 and the downstream DNA between +8 and +60 are necessary for the stimulation of promoter activity. The upstream DNA between -439 and -280 stimulates transcription in an orientation dependent manner. In the TBP promoter region, the upstream DNA between -261 and -207, and the downstream DNA between +15 and +138 are necessary for the stimulation of promoter activity. The upstream DNA (-261 to -207) required for TBP promoter activity contains a 11 bp long palindromic sequence and a DNA replication-related element sequence. Particularly, we could find that the downstream promoter regions of TFIIB and TBP genes contain the conserved nucleotide sequences, suggesting the presence of a common regulatory mechanism for the expression of these two genes.
引用
收藏
页码:770 / 776
页数:7
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