Gloy Joachim, Hikasa Hiroki, Sokol Sergei Y
Department of Microbiology and Molecular Genetics, Harvard Medical School, and Molecular Medicine Unit, Beth Israel Deaconess Medical Center, 330 Brookline Avenue, Boston, MA 02215, USA.
Nat Cell Biol. 2002 May;4(5):351-7. doi: 10.1038/ncb784.
Dishevelled (Dsh) is required for the specification of cell fate and polarity by secreted Wnt proteins. Frodo, a novel conserved Dsh-binding protein, synergized with Xenopus Dsh (XDsh) in secondary axis induction in Xenopus laevis embryos. A dominant inhibitory construct and antisense oligonucleotide-mediated depletion of Frodo inhibited axial development in response to XDsh and XWnt8, and suppressed transcriptional activation of a reporter construct. At later embryonic stages, both dominant negative Frodo and antisense oligonucleotides interfered with the expression of regional neural markers and caused eye deficiencies, indicating that Frodo is required for normal eye and neural tissue development. Full-length Frodo RNA suppressed these loss-of-function phenotypes, attesting to their specificity. These findings establish a function for Frodo as an essential positive regulator of Wnt signalling.
分泌型Wnt蛋白在细胞命运决定和极性形成过程中需要Dishevelled(Dsh)蛋白的参与。Frodo是一种新发现的保守的Dsh结合蛋白,它能与非洲爪蟾的Dsh(XDsh)协同作用,诱导非洲爪蟾胚胎产生次级轴。一种显性抑制构建体和反义寡核苷酸介导的Frodo缺失抑制了对XDsh和XWnt8的轴向发育反应,并抑制了报告构建体的转录激活。在胚胎发育后期,显性负性Frodo和反义寡核苷酸均干扰了区域神经标志物的表达并导致眼部缺陷,这表明Frodo是正常眼部和神经组织发育所必需的。全长Frodo RNA抑制了这些功能丧失表型,证明了它们的特异性。这些发现确立了Frodo作为Wnt信号通路重要正向调节因子的功能。