Letamendia A, Labbé E, Attisano L
Department of Anatomy and Cell Biology, University of Toronto, Ontario, Canada.
J Bone Joint Surg Am. 2001;83-A Suppl 1(Pt 1):S31-9.
Several studies have shown that cooperation between transforming growth factor beta (TGF-beta) and Wnt/wingless signaling pathways plays a role in controlling certain developmental events. These factors elicit their biological effects through distinct pathways in which TGF-beta and Wnt signaling induce activation of the transcriptional regulators Smads and lymphoid enhancer binding factor/T-cell-specific factor (LEF/TCF), respectively. To understand the mechanism for cooperativity between these pathways, we have investigated the molecular mechanism for this synergistic effect.
Transcriptional assays were conducted by transient transfection of HepG2 cells with use of luciferase reporter constructs. Protein/protein interaction studies were conducted in vitro with the use of glutathione-S-transferase pull-down assays and in intact cells by immunoprecipitation and immunoblotting.
We show that Smads physically interact with LEF1/TCF transcription factors and that specific DNA binding sites in the Xenopus twin promoter are required for synergistic activation by TGF-beta and Wnt pathways. In addition, we demonstrate that TGF-beta-dependent activation of LEF1/TCF target genes can occur independently of beta-catenin, an essential component of the Wnt signaling pathway.
TGF-beta and Wnt signaling pathways can independently or cooperatively regulate LEF1/TCF target genes. This suggests that the cooperation between these pathways may be important for the specification of cell fates during development.
多项研究表明,转化生长因子β(TGF-β)与Wnt/无翅信号通路之间的合作在控制某些发育事件中发挥作用。这些因子通过不同的途径引发其生物学效应,其中TGF-β和Wnt信号分别诱导转录调节因子Smads以及淋巴样增强子结合因子/T细胞特异性因子(LEF/TCF)的激活。为了解这些信号通路之间协同作用的机制,我们研究了这种协同效应的分子机制。
使用荧光素酶报告基因构建体对HepG2细胞进行瞬时转染,以进行转录分析。利用谷胱甘肽-S-转移酶下拉试验在体外进行蛋白质/蛋白质相互作用研究,并通过免疫沉淀和免疫印迹在完整细胞中进行研究。
我们发现Smads与LEF1/TCF转录因子存在物理相互作用,并且非洲爪蟾双启动子中的特定DNA结合位点是TGF-β和Wnt信号通路协同激活所必需的。此外,我们证明,LEF1/TCF靶基因的TGF-β依赖性激活可以独立于Wnt信号通路的重要组成部分β-连环蛋白而发生。
TGF-β和Wnt信号通路可以独立或协同调节LEF1/TCF靶基因。这表明这些信号通路之间的合作可能对发育过程中细胞命运的特化很重要。