| Literature DB >> 27300315 |
Min Liu1, Zhenlong Guan2, Qin Shen3, Frances Flinter4, Laura Domínguez1, Joo Wook Ahn5, David A Collier6, Timothy O'Brien1, Sanbing Shen7.
Abstract
The size of neural stem cell (NSC) pool at birth determines the starting point of adult neurogenesis. Aberrant neurogenesis is associated with major mental illness, in which ULK4 is proposed as a rare risk factor. Little is known about factors regulating the NSC pool, or function of the ULK4. Here, we showed that Ulk4(tm1a/tm1a) mice displayed a dramatically reduced NSC pool at birth. Ulk4 was expressed in a cell cycle-dependent manner and peaked in G2/M phases. Targeted disruption of the Ulk4 perturbed mid-neurogenesis and significantly reduced cerebral cortex in postnatal mice. Pathway analyses of dysregulated genes in Ulk4(tm1a/tm1a) mice revealed Ulk4 as a key regulator of cell cycle and NSC proliferation, partially through regulation of the Wnt signaling. In addition, we identified hemizygous deletion of ULK4 gene in 1.2/1,000 patients with pleiotropic symptoms including severe language delay and learning difficulties. ULK4, therefore, may significantly contribute to neurodevelopmental, neuropsychiatric, and neurodegenerative disorders. Stem Cells 2016;34:2318-2331.Entities:
Keywords: Cell cycle; Copy number variations; Neural progenitor; Neural stem cells; Neurogenesis; RNA sequencing; Ulk4; Wnt signaling
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Year: 2016 PMID: 27300315 DOI: 10.1002/stem.2423
Source DB: PubMed Journal: Stem Cells ISSN: 1066-5099 Impact factor: 6.277