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通过对受体基因家族进行多重CRISPR靶向绘制Wnt-Frizzled相互作用图谱。

Mapping of Wnt-Frizzled interactions by multiplex CRISPR targeting of receptor gene families.

作者信息

Voloshanenko Oksana, Gmach Philipp, Winter Jan, Kranz Dominique, Boutros Michael

机构信息

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.

出版信息

FASEB J. 2017 Nov;31(11):4832-4844. doi: 10.1096/fj.201700144R. Epub 2017 Jul 21.

Abstract

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.

摘要

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

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ee/5636703/07771db0e41b/fasebj201700144Rf1.jpg

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