Onai Takayuki, Matsuo-Takasaki Mami, Inomata Hidehiko, Aramaki Toshihiro, Matsumura Michiru, Yakura Rieko, Sasai Noriaki, Sasai Yoshiki
Organogenesis and Neurogenesis Group, Center for Developmental Biology, RIKEN, Chuo, Kobe, Japan.
EMBO J. 2007 May 2;26(9):2350-60. doi: 10.1038/sj.emboj.7601684. Epub 2007 Apr 12.
In Xenopus, an asymmetric distribution of Wnt activity that follows cortical rotation in the fertilized egg leads to the dorsal-ventral (DV) axis establishment. However, how a clear DV polarity develops from the initial difference in Wnt activity still remains elusive. We report here that the Teashirt-class Zn-finger factor XTsh3 plays an essential role in dorsal determination by enhancing canonical Wnt signaling. Knockdown of the XTsh3 function causes ventralization in the Xenopus embryo. Both in vivo and in vitro studies show that XTsh3 substantially enhances Wnt signaling activity in a beta-catenin-dependent manner. XTsh3 cooperatively promotes the formation of a secondary axis on the ventral side when combined with weak Wnt activity, whereas XTsh3 alone has little axis-inducing ability. Furthermore, Wnt1 requires XTsh3 for its dorsalizing activity in vivo. Immunostaining and protein analyses indicate that XTsh3 is a nuclear protein that physically associates with beta-catenin and efficiently increases the level of beta-catenin in the nucleus. We discuss the role of XTsh3 as an essential amplifying factor of canonical Wnt signaling in embryonic dorsal determination.
在非洲爪蟾中,受精卵中皮质旋转后Wnt活性的不对称分布导致背腹(DV)轴的建立。然而,Wnt活性的初始差异如何发展为清晰的DV极性仍不清楚。我们在此报告,T恤衫类锌指因子XTsh3通过增强经典Wnt信号传导在背侧决定中起关键作用。XTsh3功能的敲低导致非洲爪蟾胚胎腹化。体内和体外研究均表明,XTsh3以β-连环蛋白依赖性方式显著增强Wnt信号活性。当与弱Wnt活性结合时,XTsh3协同促进腹侧次级轴的形成,而单独的XTsh3几乎没有轴诱导能力。此外,Wnt1在体内的背化活性需要XTsh3。免疫染色和蛋白质分析表明,XTsh3是一种核蛋白,与β-连环蛋白物理结合,并有效增加细胞核中β-连环蛋白的水平。我们讨论了XTsh3作为经典Wnt信号在胚胎背侧决定中的重要放大因子的作用。