Gene structure and promoter analysis of the rat BTEB2 gene

被引:6
作者
Mori, D [1 ]
Okuro, N [1 ]
Fujii-Kuriyama, Y [1 ]
Sogawa, K [1 ]
机构
[1] Tohoku Univ, Grad Sch Life Sci, Dept Biomol Sci, Aoba Ku, Sendai, Miyagi 9808578, Japan
基金
日本学术振兴会; 日本科学技术振兴机构;
关键词
GC box; gene structure; pseudogene; transcription factor; zinc finger;
D O I
10.1016/S0378-1119(02)01203-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Rat BTEB2 protein is a transcription factor with three zinc fingers that binds to GC box, and is expressed in the placenta, intestine, and testis. To understand mechanisms of gene expression of BTEB2, we have cloned the rat BTEB2 gene from a rat liver genomic library and determined the gene structure. The BTEB2 gene contained 4 exons. In the process of cloning of the BTEB2 gene, we cloned two pseudogenes for BTEB2, one of which was a processed gene. The upstream region of the bona fide gene was fused to a luciferase reporter gene, and the generated BTEB2-luciferase chimeric plasmid was transiently transfected into HeLa cells that expressed endogenous BTEB2 mRNA. Significant expression of luciferase activity was observed. Deletion analysis of the promoter region of the BTEB2 gene revealed that at least three regions are important for the activity. Upon investigation of cis-acting elements in the regions, the GC box, CCAAT box and NF-1 binding site were found. As binding factors, Sp1, CBFa, and NF-1 were identified to the DNA elements by gel mobility shift assays using specific antibodies. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:163 / 170
页数:8
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