首页> 美国卫生研究院文献>Genetics >Structure–Function Dissection of the Frizzled Receptor in Drosophila melanogaster Suggests Different Mechanisms of Action in Planar Polarity and Canonical Wnt Signaling
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Structure–Function Dissection of the Frizzled Receptor in Drosophila melanogaster Suggests Different Mechanisms of Action in Planar Polarity and Canonical Wnt Signaling

机译:果蝇毛躁受体的结构-功能解剖表明在平面极性和规范Wnt信号作用的不同机制。

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摘要

Members of the Frizzled family of sevenpass transmembrane receptors signal via the canonical Wnt pathway and also via noncanonical pathways of which the best characterized is the planar polarity pathway. Activation of both canonical and planar polarity signaling requires interaction between Frizzled receptors and cytoplasmic proteins of the Dishevelled family; however, there has been some dispute regarding whether the Frizzled–Dishevelled interactions are the same in both cases. Studies looking at mutated forms of Dishevelled suggested that stable recruitment of Dishevelled to membranes by Frizzled was required only for planar polarity activity, implying that qualitatively different Frizzled–Dishevelled interactions underlie canonical signaling. Conversely, studies looking at the sequence requirements of Frizzled receptors in the fruit fly Drosophila melanogaster for canonical and planar polarity signaling have concluded that there is most likely a common mechanism of action. To understand better Frizzled receptor function, we have carried out a large-scale mutagenesis in Drosophila to isolate novel mutations in that affect planar polarity activity and have identified a group of missense mutations in cytosolic-facing regions of the Frizzled receptor that block Dishevelled recruitment. Interestingly, although some of these affect both planar polarity and canonical activity, as previously reported for similar lesions, we find a subset that affect only planar polarity activity. These results support the view that qualitatively different Frizzled–Dishevelled interactions underlie planar polarity and canonical Wnt signaling.
机译:七次穿越膜受体的卷曲蛋白家族成员通过经典的Wnt途径以及非经典途径(其特征最明显的是平面极性途径)发出信号。规范和平面极性信号的激活都需要卷曲的受体和Disheveled家族的细胞质蛋白之间的相互作用。但是,关于两种情况下的“翻卷—散乱”交互是否相同存在争议。研究了Disheveled的突变形式的研究表明,只有平面极性活动才需要Frizzled将Disheveled稳定地募集到膜上,这暗示着规范上不同的Frizzled-Dishevelled相互作用是基础。相反,研究果蝇果蝇中卷曲的受体对经典和平面极性信号的序列要求的研究得出结论,最有可能是一种共同的作用机制。为了更好地了解卷曲蛋白受体的功能,我们在果蝇中进行了大规模诱变,以分离出影响平面极性活性的新突变,并在卷曲蛋白受体的胞质面临区域中识别出一组阻止错乱募集的错义突变。有趣的是,尽管其中一些影响平面极性和规范活动,如先前报道的类似病变,但我们发现了一个仅影响平面极性活动的子集。这些结果支持以下观点:在平面极性和经典Wnt信号基础上,本质上不同的毛躁-杂乱的相互作用。

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