Program in Neuroscience and Mental Health, Hospital for Sick Children, Toronto, ON M5G 1L7, Canada; McEwen Center for Regenerative Medicine, University Health Network, Toronto, ON M5G 1L7, Canada.
Program in Neuroscience and Mental Health, Hospital for Sick Children, Toronto, ON M5G 1L7, Canada.
Dev Cell. 2015 Jan 12;32(1):31-42. doi: 10.1016/j.devcel.2014.11.031. Epub 2014 Dec 31.
Ankrd11 is a potential chromatin regulator implicated in neural development and autism spectrum disorder (ASD) with no known function in the brain. Here, we show that knockdown of Ankrd11 in developing murine or human cortical neural precursors caused decreased proliferation, reduced neurogenesis, and aberrant neuronal positioning. Similar cellular phenotypes and aberrant ASD-like behaviors were observed in Yoda mice carrying a point mutation in the Ankrd11 HDAC-binding domain. Consistent with a role for Ankrd11 in histone acetylation, Ankrd11 was associated with chromatin and colocalized with HDAC3, and expression and histone acetylation of Ankrd11 target genes were altered in Yoda neural precursors. Moreover, the Ankrd11 knockdown-mediated decrease in precursor proliferation was rescued by inhibiting histone acetyltransferase activity or expressing HDAC3. Thus, Ankrd11 is a crucial chromatin regulator that controls histone acetylation and gene expression during neural development, thereby providing a likely explanation for its association with cognitive dysfunction and ASD.
ANKRD11 是一种潜在的染色质调节因子,与神经发育和自闭症谱系障碍(ASD)有关,但其在大脑中的功能尚不清楚。在这里,我们发现,在发育中的小鼠或人类皮质神经前体细胞中敲低 Ankrd11 会导致增殖减少、神经发生减少和神经元位置异常。在携带 Ankrd11 HDAC 结合域点突变的 Yoda 小鼠中观察到类似的细胞表型和异常的 ASD 样行为。与 Ankrd11 参与组蛋白乙酰化的作用一致,Ankrd11 与染色质相关,并与 HDAC3 共定位,Yoda 神经前体细胞中 Ankrd11 靶基因的表达和组蛋白乙酰化发生改变。此外,通过抑制组蛋白乙酰转移酶活性或表达 HDAC3,可挽救 Ankrd11 敲低介导的前体细胞增殖减少。因此,ANKRD11 是一种关键的染色质调节因子,可在神经发育过程中控制组蛋白乙酰化和基因表达,从而为其与认知功能障碍和 ASD 的关联提供了可能的解释。