4.8 Article

Sequential phosphorylation of NDEL1 by the DYRK2-GSK3β complex is critical for neuronal morphogenesis

期刊

ELIFE
卷 8, 期 -, 页码 -

出版社

ELIFE SCIENCES PUBLICATIONS LTD
DOI: 10.7554/eLife.50850

关键词

-

类别

资金

  1. National Research Foundation of Korea [2015M3C7A1030964, 2017M3C7A1047875, 2017R1A5A1015366, 2017R1A2B2009031]
  2. Ministry of Science, ICT and Future Planning [19-BR-02-01]
  3. Canadian Institutes of Health Research
  4. National Research Foundation of Korea [2017R1A5A1015366, 2015M3C7A1030964, 2017M3C7A1047875, 2017R1A2B2009031] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Neuronal morphogenesis requires multiple regulatory pathways to appropriately determine axonal and dendritic structures, thereby to enable the functional neural connectivity. Yet, however, the precise mechanisms and components that regulate neuronal morphogenesis are still largely unknown. Here, we newly identified the sequential phosphorylation of NDEL1 critical for neuronal morphogenesis through the human kinome screening and phospho-proteomics analysis of NDEL1 from mouse brain lysate. DYRK2 phosphorylates NDEL1 S336 to prime the phosphorylation of NDEL1 S332 by GSK3 beta. TARA, an interaction partner of NDEL1, scaffolds DYRK2 and GSK3 beta to form a tripartite complex and enhances NDEL1 S336/S332 phosphorylation. This dual phosphorylation increases the filamentous actin dynamics. Ultimately, the phosphorylation enhances both axonal and dendritic outgrowth and promotes their arborization. Together, our findings suggest the NDEL1 phosphorylation at S336/S332 by the TARA-DYRK2-GSK3 beta complex as a novel regulatory mechanism underlying neuronal morphogenesis.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据