Voloshanenko Oksana, Gmach Philipp, Winter Jan, Kranz Dominique, Boutros Michael
Division of Signaling and Functional Genomics, German Cancer Research Center (DKFZ), Heidelberg, Germany; and Department of Cell and Molecular Biology, Medical Faculty Mannheim, Heidelberg University, Heidelberg, Germany
Division of Signaling and Functional Genomics, German Cancer Research Center (DKFZ), Heidelberg, Germany; and Department of Cell and Molecular Biology, Medical Faculty Mannheim, Heidelberg University, Heidelberg, Germany.
FASEB J. 2017 Nov;31(11):4832-4844. doi: 10.1096/fj.201700144R. Epub 2017 Jul 21.
Signaling pathway modules are often encoded by several closely related paralogous genes that can have redundant roles and are therefore difficult to analyze by loss-of-function analysis. A typical example is the Wnt signaling pathway, which in mammals is mediated by 19 Wnt ligands that can bind to 10 Frizzled (FZD) receptors. Although significant progress in understanding Wnt-FZD receptor interactions has been made in recent years, tools to generate systematic interaction maps have been largely lacking. Here we generated cell lines with multiplex mutant alleles of , , and and demonstrate that these cells are unresponsive to canonical Wnt ligands. Subsequently, we performed genetic rescue experiments with combinations of FZDs and canonical Wnts to create a functional ligand-receptor interaction map. These experiments showed that whereas several Wnt ligands, such as Wnt3a, induce signaling through a broad spectrum of FZD receptors, others, such as Wnt8a, act through a restricted set of genes. Together, our results map functional interactions of FZDs and 10 Wnt ligands and demonstrate how multiplex targeting by clustered regularly interspaced short palindromic repeat (CRISPR)/Cas9 can be used to systematically elucidate the functions of multigene families.-Voloshanenko, O., Gmach, P., Winter, J., Kranz, D., Boutros, M. Mapping of Wnt-Frizzled interactions by multiplex CRISPR targeting of receptor gene families.
信号通路模块通常由几个密切相关的旁系同源基因编码,这些基因可能具有冗余作用,因此难以通过功能缺失分析进行研究。一个典型的例子是Wnt信号通路,在哺乳动物中,该通路由19种Wnt配体介导,这些配体可与10种卷曲蛋白(FZD)受体结合。尽管近年来在理解Wnt-FZD受体相互作用方面取得了重大进展,但生成系统相互作用图谱的工具却一直非常缺乏。在这里,我们构建了具有 、 和 多重突变等位基因的细胞系,并证明这些细胞对经典Wnt配体无反应。随后,我们用FZDs和经典Wnts的组合进行了基因拯救实验,以创建一个功能性配体-受体相互作用图谱。这些实验表明,虽然几种Wnt配体,如Wnt3a,可通过多种FZD受体诱导信号传导,但其他配体,如Wnt8a,则通过一组有限的 基因起作用。总之,我们的结果绘制了FZDs与10种Wnt配体之间的功能相互作用图谱,并证明了如何通过成簇规律间隔短回文重复序列(CRISPR)/Cas9多重靶向来系统地阐明多基因家族的功能。-沃洛沙年科,O.,格马赫,P.,温特,J.,克兰兹,D.,布特罗斯,M.通过受体基因家族的多重CRISPR靶向绘制Wnt-卷曲蛋白相互作用图谱