| Literature DB >> 33020269 |
Lei Zhang1, Hongyang Jing1, Haiwen Li1, Wenbing Chen1, Bin Luo1, Hongsheng Zhang1, Zhaoqi Dong1, Lei Li1, Huabo Su2, Wen-Cheng Xiong1,3, Lin Mei4,3.
Abstract
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.Entities:
Keywords: Nae1; Wnt/β-catenin signaling; cerebral cortex; neddylation; progenitor
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Year: 2020 PMID: 33020269 PMCID: PMC7584916 DOI: 10.1073/pnas.2005395117
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205