Hilton Emma, Rex Maria, Old Robert
Biomolecular Medicine Group, Department of Biological Sciences, University of Warwick, Gibbet Hill Road, Coventry CV4 7AL, UK.
Mech Dev. 2003 Oct;120(10):1127-38. doi: 10.1016/j.mod.2003.08.004.
Xenopus Nodal-related (Xnr) 5 is one of the earliest expressed components of a network of TGF-beta factors participating in endoderm and mesoderm formation. Zygotic gene expression is not required for induction of Xnr5; rather, expression is dependent on the maternal factors VegT, localised throughout the vegetal pole, and beta-catenin, functional in the future dorsal region of the embryo. Using transient assays with a luciferase reporter in Xenopus embryos, we have defined a minimal promoter, which mimics the response of the endogenous gene to applied factors. Expression of luciferase from the minimal promoter is dorsal-specific and requires two T-box half sites and a functional beta-catenin/XTcf-3 pathway. Mutation of two Tcf/Lef sites in the minimal promoter permits induction by VegT to wild-type promoter levels in the presence of a dominant-negative XTcf-3, indicating that beta-catenin/XTcf-3 are repressive and are not required as transactivators of Xnr5 transcription. The activity of the Tcf/Lef mutant promoter is similar in both ventral and dorsal sides of the embryo. In transgenic experiments, the dorsal specificity of expression of a beta-gal reporter driven by the wild-type minimal promoter is abolished upon mutation of these Tcf/Lef sites. We propose a model in which XTcf-3 functions as a repressor of Xnr5 throughout the blastula embryo, except where repression is lifted by the binding of beta-catenin in the dorsal region. This removal of repression allows activation of the promoter by VegT in the dorsal vegetal region. Subsequently, zygotically expressed LEF1 supersedes the role of beta-catenin/XTcf-3.
非洲爪蟾Nodal相关蛋白(Xnr)5是参与内胚层和中胚层形成的转化生长因子β(TGF-β)因子网络中最早表达的成分之一。诱导Xnr5并不需要合子基因表达;相反,其表达依赖于母体因子VegT(定位于整个植物极)和β-连环蛋白(在胚胎未来的背侧区域起作用)。通过在非洲爪蟾胚胎中使用荧光素酶报告基因进行瞬时分析,我们确定了一个最小启动子,它模拟了内源基因对所施加因子的反应。最小启动子驱动的荧光素酶表达具有背侧特异性,并且需要两个T-box半位点和一条功能性的β-连环蛋白/XTcf-3信号通路。最小启动子中两个Tcf/Lef位点的突变允许在存在显性负性XTcf-3的情况下,由VegT诱导至野生型启动子水平,这表明β-连环蛋白/XTcf-3起抑制作用,而不是作为Xnr5转录的反式激活因子所必需。Tcf/Lef突变启动子的活性在胚胎的腹侧和背侧均相似。在转基因实验中,当这些Tcf/Lef位点发生突变时,由野生型最小启动子驱动的β-半乳糖苷酶报告基因表达的背侧特异性就会消失。我们提出了一个模型,其中XTcf-3在整个囊胚期胚胎中作为Xnr5的抑制因子起作用,除了在背侧区域β-连环蛋白结合解除抑制的地方。这种抑制的解除允许VegT在背侧植物区域激活启动子。随后,合子表达型LEF1取代了β-连环蛋白/XTcf-3的作用。