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

被引:49
|
作者
Durak, O. [1 ]
de Anda, F. C. [1 ]
Singh, K. K. [1 ]
Leussis, M. P. [2 ,3 ,4 ,5 ,6 ]
Petryshen, T. L. [2 ,3 ,4 ,5 ,6 ]
Sklar, P. [7 ,8 ,9 ]
Tsai, L-H [1 ]
机构
[1] MIT, Picower Inst Learning & Memory, Dept Brain & Cognit Sci, Cambridge, MA 02139 USA
[2] Massachusetts Gen Hosp, Psychiat & Neurodevelopmental Genet Unit, Ctr Human Genet Res, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Dept Psychiat, Boston, MA 02114 USA
[4] Harvard Univ, Sch Med, Dept Psychiat, Boston, MA 02115 USA
[5] Broad Inst Harvard, Stanley Ctr Psychiat Res, Cambridge, MA USA
[6] MIT, Cambridge, MA 02139 USA
[7] Mt Sinai Sch Med, Div Psychiat Genom, Dept Psychiat, New York, NY USA
[8] Mt Sinai Sch Med, Dept Neurosci, New York, NY USA
[9] Mt Sinai Sch Med, Dept Genet & Genom Sci, New York, NY USA
关键词
GENOME-WIDE ASSOCIATION; BIPOLAR-DISORDER; CORTICAL DEVELOPMENT; INITIAL SEGMENT; RISK VARIANT; E-CADHERIN; SCHIZOPHRENIA; CELL; ANK3; PATHWAY;
D O I
10.1038/mp.2014.42
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:388 / 397
页数:10
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