Department of Genetics, Albert Einstein College of Medicine, Bronx, New York, USA.
Dev Dyn. 2010 Jun;239(6):1708-22. doi: 10.1002/dvdy.22308.
To understand the mechanism by which canonical Wnt signaling sets boundaries for pattern formation in the otic vesicle (OV), we examined Tbx1 and Eya1-Six1 downstream of activated beta-catenin. Tbx1, the gene for velo-cardio-facial syndrome/DiGeorge syndrome (VCFS/DGS), is essential for inner ear development where it promotes Bmp4 and Otx1 expression and restricts neurogenesis. Using floxed beta-catenin gain-of-function (GOF) and loss-of-function (LOF) alleles, we found Tbx1 expression was down-regulated and maintained/enhanced in the two mouse mutants, respectively. Bmp4 was ectopically expressed and Otx1 was lost in beta-catenin GOF mutants. Normally, inactivation of Tbx1 causes expanded neurogenesis, but expression of NeuroD was down-regulated in beta-catenin GOF mutants. To explain this paradox, Eya1 and Six1, genes for branchio-oto-renal (BOR) syndrome were down-regulated in the OV of beta-catenin GOF mutants independently of Tbx1. Overall, this work helps explain the mechanism by which Wnt signaling modulates transcription factors required for neurogenesis and patterning of the OV.
为了理解经典 Wnt 信号在耳泡(OV)中为形态发生设定边界的机制,我们研究了激活的β-连环蛋白下游的 Tbx1 和 Eya1-Six1。Tbx1 是心脏面部综合征/ DiGeorge 综合征(VCFS/DGS)的基因,对于内耳发育至关重要,它促进 Bmp4 和 Otx1 的表达并限制神经发生。使用 floxed β-连环蛋白功能获得(GOF)和功能丧失(LOF)等位基因,我们发现 Tbx1 表达分别在两种小鼠突变体中下调和维持/增强。Bmp4 在β-连环蛋白 GOF 突变体中异位表达,而 Otx1 丢失。通常,Tbx1 的失活会导致神经发生扩张,但在β-连环蛋白 GOF 突变体中,NeuroD 的表达下调。为了解释这一矛盾,BOR 综合征的基因 Eya1 和 Six1 在β-连环蛋白 GOF 突变体的 OV 中独立于 Tbx1 下调。总的来说,这项工作有助于解释 Wnt 信号如何调节神经发生和 OV 模式形成所需的转录因子。