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Both ciliary and non-ciliary functions of Foxj1a confer Wnt/β-catenin signaling in zebrafish left-right patterning

机译:Foxj1a的睫状和非睫状功能均在斑马鱼左右模式中赋予Wnt /β-catenin信号传导

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The Wnt/β-catenin pathway is implicated in left-right (LR) axis determination; however, the underlying mechanism remains elusive. Prompted by our recent discovery that Wnt signaling regulates ciliogenesis in the zebrafish Kupffer's vesicle (KV) via Foxj1a, a ciliogenic transcription factor, we decided to elucidate functions of Foxj1a in Wnt-regulated LR pattern formation. We showed that targeted injection of wnt8a mRNA into a single cell at the 128-cell stage is sufficient to induce ectopic foxj1a expression and ectopic cilia. By interrogating the transcription circuit of foxj1a regulation, we found that both Lef1 and Tcf7 bind to a consensus element in the foxj1a promoter region. Depletion of Lef1 and Tcf7 inhibits foxj1a transcription in the dorsal forerunner cells, downregulates cilia length and number in KV, and randomizes LR asymmetry. Targeted overexpression of a constitutively active form of Lef1 also induced an ectopic protrusion that contains ectopic transcripts for sox17 , foxj1a , and charon , and ectopic monocilia. Further genetic studies using this ectopic expression platform revealed two distinct functions of Foxj1a; mediating Wnt-governed monocilia length elongation as well as charon transcription. The novel Foxj1a- charon regulation is conserved in KV, and importantly, it is independent of the canonical role of Foxj1a in the biosynthesis of motile cilia. Together with the known function of motile cilia movement in generating asymmetric expression of charon , our data put forward a hypothesis that Foxj1a confers both ciliary and non-ciliary functions of Wnt signaling, which converge on charon to regulate LR pattern formation.
机译:Wnt /β-catenin途径与左右(LR)轴的测定有关。但是,基本机制仍然难以捉摸。根据我们最近的发现提示,Wnt信号通过一个纤毛发生转录因子Foxj1a调节斑马鱼库普弗囊泡(KV)的纤毛发生,我们决定阐明Foxj1a在Wnt调控的LR模式形成中的功能。我们表明,将wnt8a mRNA定向注射到128细胞阶段的单个细胞中足以诱导异位foxj1a表达和异位纤毛。通过询问foxj1a调控的转录回路,我们发现Lef1和Tcf7都与foxj1a启动子区域的共有元件结合。 Lef1和Tcf7的耗竭抑制了背部前体细胞中的foxj1a转录,下调了纤毛的长度和KV数量,并使LR不对称随机化。有针对性的Lef1活性形式的过表达也诱导了异位突起,该异位突起包含sox17,foxj1a和charon的异位转录本,以及异位单纤毛。使用该异位表达平台的进一步遗传研究显示了Foxj1a的两个不同功能。介导Wnt控制的单纤毛长度延长以及charon转录。新的Foxj1a-charon调节在KV中是保守的,重要的是,它独立于Foxj1a在能动纤毛的生物合成中的典型作用。连同运动的纤毛运动在产生不对称表达的charon中的已知功能一起,我们的数据提出了一个假设,即Foxj1a赋予Wnt信号的纤毛和非纤毛功能,它们会收敛在charon上以调节LR模式的形成。

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