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在非洲爪蟾囊胚中,早期合子基因Xnr5的VegT激活需要解除Tcf介导的抑制作用。

VegT activation of the early zygotic gene Xnr5 requires lifting of Tcf-mediated repression in the Xenopus blastula.

作者信息

Hilton Emma, Rex Maria, Old Robert

机构信息

Biomolecular Medicine Group, Department of Biological Sciences, University of Warwick, Gibbet Hill Road, Coventry CV4 7AL, UK.

出版信息

Mech Dev. 2003 Oct;120(10):1127-38. doi: 10.1016/j.mod.2003.08.004.

DOI:10.1016/j.mod.2003.08.004
PMID:14568102
Abstract

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.

摘要

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。

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