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Neddylation is critical to cortical development by regulating Wnt/β-catenin signaling.
- Source :
-
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2020 Oct 20; Vol. 117 (42), pp. 26448-26459. Date of Electronic Publication: 2020 Oct 05. - Publication Year :
- 2020
-
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.<br />Competing Interests: The authors declare no competing interest.
- Subjects :
- Animals
Cell Differentiation physiology
Cell Proliferation
Cerebral Cortex metabolism
Female
Male
Mice
NEDD8 Protein genetics
Neural Stem Cells metabolism
Neurogenesis physiology
Neurons metabolism
Signal Transduction physiology
Ubiquitin-Activating Enzymes genetics
Ubiquitin-Activating Enzymes metabolism
Wnt Signaling Pathway physiology
beta Catenin metabolism
NEDD8 Protein metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1091-6490
- Volume :
- 117
- Issue :
- 42
- Database :
- MEDLINE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Publication Type :
- Academic Journal
- Accession number :
- 33020269
- Full Text :
- https://doi.org/10.1073/pnas.2005395117