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Neddylation is critical to cortical development by regulating Wnt/β-catenin signaling
Author(s) -
Lei Zhang,
Hongyang Jing,
Philip L. Bailin,
Wenbing Chen,
Bin Luo,
Hongsheng Zhang,
Zhaoqi Dong,
Lei Li,
Huabo Su,
WenCheng Xiong,
Lin Mei
Publication year - 2020
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.2005395117
Subject(s) - neddylation , wnt signaling pathway , microbiology and biotechnology , neocortex , catenin , neurogenesis , ubiquitin , biology , progenitor cell , wnt3a , signal transduction , neuroscience , stem cell , genetics , ubiquitin ligase , gene
Wnt signaling plays a critical role in production and differentiation of neurons and undergoes a progressive reduction during cortical development. However, how Wnt signaling is regulated is not well understood. Here we provide evidence for an indispensable role of neddylation, a ubiquitylation-like protein modification, in inhibiting Wnt/β-catenin signaling. We show that β-catenin is neddylated; and inhibiting β-catenin neddylation increases its nuclear accumulation and Wnt/β-catenin signaling. To test this hypothesis in vivo, we mutated Nae1, an obligative subunit of the E1 for neddylation in cortical progenitors. The mutation leads to eventual reduction in radial glia progenitors (RGPs). Consequently, the production of intermediate progenitors (IPs) and neurons is reduced, and neuron migration is impaired, resulting in disorganization of the cerebral cortex. These phenotypes are similar to those of β-catenin gain-of-function mice. Finally, suppressing β-catenin expression is able to rescue deficits of Nae1 mutant mice. Together, these observations identified a mechanism to regulate Wnt/β-catenin signaling in cortical development.

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