Identification of putative transcription factor binding sites in rodent selenoprotein W promoter

被引:8
作者
Amantana, A
Vorachek, WR
Butler, JA
Ream, W
Whanger, PD
机构
[1] Oregon State Univ, Dept Environm & Mol Toxicol, Corvallis, OR 97331 USA
[2] Oregon State Univ, Dept Microbiol, Corvallis, OR 97331 USA
关键词
selenoprotein W promoter; transcriptional regulation; specificity protein 1; C6; cells;
D O I
10.1016/j.jinorgbio.2004.06.003
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
To understand transcriptional regulation of the selenoprotein W (SeW) gene, we used in vitro binding assays to identify transcription factors that may be involved in the transcriptional regulation of the SeW gene. Using protein from rat C6 (glial) cell nuclear extracts, oligonucleotides containing putative regulatory elements in the SeW promoter and antibodies, we observed that specificity protein 1(Sp1) transcription factor binds to the Sp1 consensus sequence in the SeW promoter as well as to the metal response element (MRE). Although competition analysis showed specific binding at the TFII-1 site, super-shift analysis using anti-TFII-1 antibody did not yield any super-shifted band. Therefore, the SeW gene may be a target for Sp1 whose binding to various regulatory sequences of the SeW promoter may activate or repress the transcription of SeW. The MRE, GRE, AP-1 and LF-A1 sites were also tested but no evidence was obtained for specific binding as indicated by lack of competition with unlabeled probes. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1513 / 1520
页数:8
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