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DKK1的三维结构表明其参与了经典和非经典Wnt信号通路。

[3D structure of DKK1 indicates its involvement in both canonical and non-canonical Wnt pathways].

作者信息

Khalili S, Rasaee M J, Bamdad T

机构信息

Department of Medical Biotechnology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

Department of Virology, School of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

出版信息

Mol Biol (Mosk). 2017 Jan-Feb;51(1):180-192. doi: 10.7868/S0026898417010098.

Abstract

Dikkoppf-1 (DKK1) is an antagonist of the canonical Wnt signaling pathway. The importance of DKK1 as a diagnostic and therapeutic agent in a wide range of diseases along with its significance in a variety of biological processes accentuate the necessity to decipher its 3D structure that would pave the way towards the development of relevant selective inhibitors. A DKK1 structure model predicted by the Robetta server with structural refinements including a 10 ns molecular dynamics run was subjected to functional and docking analyses. We hypothesize that the N-terminal region of the DKK1 molecule could be functionally important for both canonical and noncanonical Wnt pathways. Moreover, it seems that DKK1 could be involved in interactions with the Frizzled receptors, leading to the activation of the Planar Cell Polarity (PCP) pathway (activation of Jun N-terminal kinase (JNK) Pathway) and Wnt/Ca^(2+) pathway (activation of CamKII).

摘要

Dickkopf-1(DKK1)是经典Wnt信号通路的拮抗剂。DKK1作为多种疾病的诊断和治疗剂的重要性及其在各种生物过程中的意义,凸显了解析其三维结构的必要性,这将为开发相关的选择性抑制剂铺平道路。由Robetta服务器预测并经过包括10纳秒分子动力学运行在内的结构优化的DKK1结构模型,进行了功能和对接分析。我们假设DKK1分子的N端区域对于经典和非经典Wnt通路在功能上可能都很重要。此外,DKK1似乎可能参与与卷曲受体的相互作用,导致平面细胞极性(PCP)通路(Jun N端激酶(JNK)通路激活)和Wnt/Ca²⁺通路(钙/钙调蛋白依赖性蛋白激酶II(CamKII)激活)的激活。

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