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SMAD介导的YY1活性调节对BMP反应及GATA4/5/6依赖性鸡Nkx2.5增强子的心脏特异性表达的调控。

SMAD-mediated modulation of YY1 activity regulates the BMP response and cardiac-specific expression of a GATA4/5/6-dependent chick Nkx2.5 enhancer.

作者信息

Lee Kyu-Ho, Evans Samuel, Ruan Todd Y, Lassar Andrew B

机构信息

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, 240 Longwood Avenue Boston, MA 02115, USA.

出版信息

Development. 2004 Oct;131(19):4709-23. doi: 10.1242/dev.01344. Epub 2004 Aug 25.

DOI:10.1242/dev.01344
PMID:15329343
Abstract

Prior work has indicated that BMP signals act in concert with FGF8, WNT11 and WNT antagonists to induce the formation of cardiac tissue in the vertebrate embryo. In an effort to understand how these signaling pathways control the expression of key cardiac regulators, we have characterized the cis-regulatory elements of the chick tinman homolog chick Nkx2.5. We find that at least three distinct cardiac activating regions (CARs) of chick Nkx2.5 cooperate to regulate early expression in the cardiac crescent and later segmental expression in the developing heart. In this report, we focus our attention on a 3' BMP-responsive enhancer, termed CAR3, which directs robust cardiac transgene expression. By systematic mutagenesis and gel shift analysis of this enhancer, we demonstrate that GATA4/5/6, YY1 and SMAD1/4 are all necessary for BMP-mediated induction and heart-specific expression of CAR3. Adjacent YY1 and SMAD-binding sites within CAR3 constitute a minimal BMP response element, and interaction of SMAD1/4 with the N terminus of YY1 is required for BMP-mediated induction of CAR3. Our data suggest that BMP-mediated activation of this regulatory region reflects both the induction of GATA genes by BMP signals, as well as modulation of the transcriptional activity of YY1 by direct interaction of this transcription factor with BMP-activated SMADs.

摘要

先前的研究表明,骨形态发生蛋白(BMP)信号与成纤维细胞生长因子8(FGF8)、无翅型MMTV整合位点家族成员11(WNT11)及WNT拮抗剂协同作用,诱导脊椎动物胚胎心脏组织的形成。为了了解这些信号通路如何控制关键心脏调节因子的表达,我们对鸡tinman同源物鸡Nkx2.5的顺式调控元件进行了表征。我们发现,鸡Nkx2.5的至少三个不同的心脏激活区域(CARs)协同调节心脏新月区的早期表达以及发育中心脏的后期节段性表达。在本报告中,我们将注意力集中在一个3' BMP反应增强子,称为CAR3,它可指导强大的心脏转基因表达。通过对该增强子进行系统诱变和凝胶迁移分析,我们证明GATA4/5/6、YY1和SMAD1/4对于BMP介导的CAR3诱导和心脏特异性表达都是必需的。CAR3内相邻的YY1和SMAD结合位点构成了一个最小的BMP反应元件,BMP介导的CAR3诱导需要SMAD1/4与YY1的N末端相互作用。我们的数据表明,BMP介导的该调控区域的激活既反映了BMP信号对GATA基因的诱导,也反映了该转录因子与BMP激活的SMAD直接相互作用对YY1转录活性的调节。

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