4.8 Article

Ankyrin-G regulates neurogenesis and Wnt signaling by altering the subcellular localization of β-catenin

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MOLECULAR PSYCHIATRY
卷 20, 期 3, 页码 388-397

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NATURE PUBLISHING GROUP
DOI: 10.1038/mp.2014.42

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  1. Simons Foundation (Simons Center for the Social Brain, Massachusetts Institute of Technology)
  2. NIH RO1 Grant [MH091115]
  3. Stanley Medical Research Institute
  4. Howard Hughes Medical Institute

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Ankyrin-G is a scaffolding protein required for the formation of the axon initial segment in neurons. Recent genome-wide association studies and whole-exome sequencing have identified ANK3, the gene coding for ankyrin-G, to be a risk gene for multiple neuropsychiatric disorders, such as bipolar disorder, schizophrenia and autism spectrum disorder. Here, we describe a novel role for ankyrin-G in neural progenitor proliferation in the developing cortex. We found that ankyrin-G regulates canonical Wnt signaling by altering the subcellular localization and availability of beta-catenin in proliferating cells. Ankyrin-G loss-of-function increases beta-catenin levels in the nucleus, thereby promoting neural progenitor proliferation. Importantly, abnormalities in proliferation can be rescued by reducing Wnt pathway signaling. Taken together, these results suggest that ankyrin-G is required for proper brain development.

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