Suppr超能文献

Wnt配体依赖性负反馈调节因子Nkd1的激活

Wnt ligand-dependent activation of the negative feedback regulator Nkd1.

作者信息

Larraguibel Jahdiel, Weiss Alexander R E, Pasula Daniel J, Dhaliwal Rasmeet S, Kondra Roman, Van Raay Terence J

机构信息

Department of Molecular and Cellular Biology, University of Guelph, Guelph, ON N1G 2W1, Canada.

Department of Molecular and Cellular Biology, University of Guelph, Guelph, ON N1G 2W1, Canada

出版信息

Mol Biol Cell. 2015 Jun 15;26(12):2375-84. doi: 10.1091/mbc.E14-12-1648. Epub 2015 Apr 22.

Abstract

Misregulation of Wnt signaling is at the root of many diseases, most notably colorectal cancer, and although we understand the activation of the pathway, we have a very poor understanding of the circumstances under which Wnt signaling turns itself off. There are numerous negative feedback regulators of Wnt signaling, but two stand out as constitutive and obligate Wnt-induced regulators: Axin2 and Nkd1. Whereas Axin2 behaves similarly to Axin in the destruction complex, Nkd1 is more enigmatic. Here we use zebrafish blastula cells that are responsive Wnt signaling to demonstrate that Nkd1 activity is specifically dependent on Wnt ligand activation of the receptor. Furthermore, our results support the hypothesis that Nkd1 is recruited to the Wnt signalosome with Dvl2, where it becomes activated to move into the cytoplasm to interact with β-catenin, inhibiting its nuclear accumulation. Comparison of these results with Nkd function in Drosophila generates a unified and conserved model for the role of this negative feedback regulator in the modulation of Wnt signaling.

摘要

Wnt信号通路的失调是许多疾病的根源,最显著的是结直肠癌,尽管我们了解该信号通路的激活过程,但对于Wnt信号通路自我关闭的情况却知之甚少。Wnt信号通路有许多负反馈调节因子,但有两个作为组成型且必需的Wnt诱导调节因子尤为突出:Axin2和Nkd1。虽然Axin2在破坏复合物中的行为与Axin相似,但Nkd1则更为神秘。在这里,我们使用对Wnt信号有反应的斑马鱼囊胚细胞来证明Nkd1的活性特别依赖于受体的Wnt配体激活。此外,我们的结果支持这样的假设,即Nkd1与Dvl2一起被招募到Wnt信号小体中,在那里它被激活并进入细胞质与β-连环蛋白相互作用,抑制其核内积累。将这些结果与Nkd在果蝇中的功能进行比较,为这种负反馈调节因子在Wnt信号通路调节中的作用产生了一个统一且保守的模型。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验