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Smad6是一种由Smad1/5诱导产生的Smad抑制剂。小鼠Smad6启动子中骨形态发生蛋白反应元件的特征。

Smad6 is a Smad1/5-induced smad inhibitor. Characterization of bone morphogenetic protein-responsive element in the mouse Smad6 promoter.

作者信息

Ishida W, Hamamoto T, Kusanagi K, Yagi K, Kawabata M, Takehara K, Sampath T K, Kato M, Miyazono K

机构信息

Department of Biochemistry, Cancer Institute of the Japanese Foundation for Cancer Research (JFCR), and Research for the Future Program, Japan Society for the Promotion of Science, 1-37-1 Kami-ikebukuro, Toshima-ku, Tokyo 170-8455, Japan.

出版信息

J Biol Chem. 2000 Mar 3;275(9):6075-9. doi: 10.1074/jbc.275.9.6075.

Abstract

Smad6 is an inhibitory Smad that is induced by bone morphogenetic proteins (BMPs) and interferes with BMP signaling. We have isolated the mouse Smad6 promoter and identified the regions responsible for transcriptional activation by BMPs. The proximal BMP-responsive element (PBE) in the Smad6 promoter is important for the transcriptional activation by BMPs and contains a 28-base pair GC-rich sequence including four overlapping copies of the GCCGnCGC-like motif, which is a binding site for Drosophila Mad and Medea. We generated a luciferase reporter construct (3GC2-Lux) containing three repeats of the GC-rich sequence derived from the PBE. BMPs and BMP receptors induced transcriptional activation of 3GC2-Lux in various cell types, and this activation was enhanced by cotransfection of BMP-responsive Smads, i.e. Smad1 or Smad5. Moreover, direct DNA binding of BMP-responsive Smads and common-partner Smad4 to the GC-rich sequence of PBE was observed. These results indicate that the expression of Smad6 is regulated by the effects of BMP-activated Smad1/5 on the Smad6 promoter.

摘要

Smad6是一种抑制性Smad,由骨形态发生蛋白(BMP)诱导产生,并干扰BMP信号传导。我们分离出了小鼠Smad6启动子,并确定了负责BMP转录激活的区域。Smad6启动子中的近端BMP反应元件(PBE)对BMP的转录激活很重要,它包含一个28个碱基对的富含GC的序列,其中包括四个重叠的GCCGnCGC样基序拷贝,这是果蝇Mad和Medea的结合位点。我们构建了一个荧光素酶报告基因载体(3GC2-Lux),它含有三个源自PBE的富含GC序列的重复片段。BMP和BMP受体在各种细胞类型中诱导了3GC2-Lux的转录激活,并且通过共转染BMP反应性Smad,即Smad1或Smad5,这种激活作用得到增强。此外,还观察到BMP反应性Smad和共同伙伴Smad4与PBE的富含GC序列直接结合。这些结果表明,Smad6的表达受BMP激活的Smad1/5对Smad6启动子作用的调控。

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