MRC Centre for Developmental and Biomedical Genetics, and Department of Biomedical Science, University of Sheffield, Sheffield, S10 2TN, United Kingdom.
Genetics. 2012 Dec;192(4):1295-313. doi: 10.1534/genetics.112.144592. Epub 2012 Sep 28.
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 frizzled 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.
卷曲家族的七个成员 7 次跨膜受体通过经典的 Wnt 途径以及最佳特征的非经典途径信号转导,其中非经典途径是平面极性途径。经典和平面极性信号的激活都需要卷曲受体和盘状蛋白家族的细胞质蛋白之间的相互作用;然而,关于卷曲-盘状蛋白相互作用在这两种情况下是否相同,一直存在一些争议。研究表明,盘状蛋白的突变形式表明,卷曲蛋白仅需要稳定地将盘状蛋白募集到膜上,才能进行平面极性活性,这意味着经典信号转导的卷曲-盘状蛋白相互作用在质上是不同的。相反,研究果蝇中卷曲受体在经典和平面极性信号中的序列要求得出的结论是,很可能存在一种共同的作用机制。为了更好地理解卷曲受体的功能,我们在果蝇中进行了大规模的诱变,以分离影响平面极性活性的新突变,并鉴定出一组卷曲受体胞质面区域的错义突变,这些突变会阻断盘状蛋白的募集。有趣的是,尽管其中一些突变既影响平面极性又影响经典活性,就像以前报道的类似病变一样,我们发现了一组仅影响平面极性活性的突变。这些结果支持了这样一种观点,即平面极性和经典 Wnt 信号转导的卷曲-盘状蛋白相互作用在质上是不同的。