Ikeda Toshiyuki, Saito Taku, Ushita Masahiro, Yano Fumiko, Kan Akinori, Itaka Keiji, Moro Toru, Nakamura Kozo, Kawaguchi Hiroshi, Chung Ung-Il
Sensory and Motor System Medicine, Faculty of Medicine, University of Tokyo, Hongo 7-3-1, Bunkyo, Tokyo 113-8655, Japan.
Biochem Biophys Res Commun. 2007 Jun 1;357(2):383-90. doi: 10.1016/j.bbrc.2007.03.133. Epub 2007 Apr 2.
The present study attempted to identify and characterize the embryonic promoter of Sox6, a determinant regulator of chondrogenic differentiation. A common transcription start region for human and mouse Sox6 was initially identified, which contained a highly conserved sequence, A-box. Tandem repeats of A-box had a strong transcriptional activity both at the basal level and in response to Sox9. Cells carrying the 4xA-box-DsRed2 reporter fluoresced only upon chondrogenic differentiation. The 46-bp core enhancer region (CES6) was then identified in the 3' half of A-box, within which a C/EBP-binding motif was identified. Overexpressed C/EBPbeta activated the Sox6 promoter, and mutant 4xCES6 constructs lacking the C/EBP motif lost their basal activity. CES6 and nuclear extracts formed a specific complex, which was supershifted by anti-C/EBPbeta antibody, and in vitro translated C/EBPbeta specifically bound to CES6. Thus, we successfully identified the Sox6 promoter and its core enhancer and characterized the interactions with regulatory transcription factors.
本研究试图鉴定并表征Sox6的胚胎启动子,Sox6是软骨形成分化的决定性调节因子。最初鉴定出人类和小鼠Sox6的一个共同转录起始区域,其包含一个高度保守的序列,即A盒。A盒的串联重复在基础水平以及对Sox9的应答中均具有强大的转录活性。携带4xA盒-DsRed2报告基因的细胞仅在软骨形成分化时发出荧光。随后在A盒的3' 半区鉴定出46个碱基对的核心增强子区域(CES6),在该区域内鉴定出一个C/EBP结合基序。过表达的C/EBPβ激活Sox6启动子,而缺乏C/EBP基序的突变4xCES6构建体失去其基础活性。CES6与核提取物形成特异性复合物,该复合物被抗C/EBPβ抗体超迁移,并且体外翻译的C/EBPβ特异性结合CES6。因此,我们成功鉴定了Sox6启动子及其核心增强子,并表征了与调节转录因子的相互作用。