Lef1 regulates COX-2 transcription in chondrocytes

被引:21
|
作者
Yun, Kangsun [1 ]
Im, Sin-Hyeog [1 ]
机构
[1] GIST, Dept Life Sci, Kwangju 500712, South Korea
关键词
COX-2; Lef1; beta-catenin; interleukin-1; beta; chondrocytes; transcription;
D O I
10.1016/j.bbrc.2007.09.129
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
Although the involvement of Wnt/beta-catenin signaling pathway in the regulation of COX-2 expression has been suggested, the underlying molecular mechanisms are still unclear. Here, we demonstrate that lymphoid enhancer-binding factor 1 (Left) in concert with P-catenin is associated with the transcriptional regulation of the gene encoding COX-2 in mouse chondrocytes. Our results show that co-overexpression of Left and P-catenin synergistically upregulates COX-2 expression. Furthermore, decrease of Left expression using Left siRNA results in the downregulation of COX-2 expression. Using bioinformatic analysis, we identified a conserved Lef1-binding site that is mapped at the 3' region of the genomic COX-2 locus. In vivo and in vitro binding of Left at the predicted binding site was proved using chromatin immunoprecipitation assays and electrophoretic mobility shift assays, respectively. Moreover, binding of Left and P-catenin to the Lef1-binding site transactivates COX-2 promoter activity. Our results indicate a pivotal role of Left in the regulation of COX-2 transcription in arthritic chondrocytes. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:270 / 275
页数:6
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