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与自闭症相关的ANK2调节胚胎神经发育。

Autism-associated ANK2 regulates embryonic neurodevelopment.

作者信息

Kawano Shotaro, Baba Masayuki, Fukushima Hotaka, Miura Daiki, Hashimoto Hitoshi, Nakazawa Takanobu

机构信息

Laboratory of Molecular Biology, Department of Bioscience, Graduate School of Life Sciences, Tokyo University of Agriculture, Tokyo, 156-8502, Japan.

Laboratory of Molecular Neuropharmacology, Graduate School of Pharmaceutical Sciences, Osaka University, Suita, Osaka, 565-0871, Japan.

出版信息

Biochem Biophys Res Commun. 2022 May 21;605:45-50. doi: 10.1016/j.bbrc.2022.03.058. Epub 2022 Mar 12.

DOI:10.1016/j.bbrc.2022.03.058
PMID:35313230
Abstract

Autism spectrum disorder (ASD) is a neurodevelopmental condition characterized by altered social communication, restricted interests, and stereotypic behaviors. Although the molecular and cellular pathogeneses of ASD remain elusive, impaired neural stem cell differentiation and neuronal migration during cortical development are suggested to be critically involved in ASD. ANK2, which encodes for a cytoskeletal scaffolding protein involved in recruiting membrane proteins into specialized membrane domains, has been identified as a high-confidence ASD risk gene. However, the role of ANK2 in early neural development remains unclear. In this study, we analyzed the role of ANK2 in the cerebral cortex of developing mouse using in utero electroporation. We provide evidence suggesting that ANK2 regulates neural stem cell differentiation and neuronal migration in the embryonic cerebral cortex, where Ank2 is highly expressed. We also demonstrated that Ank2 knockdown alters the expression of genes involved in neural development. Taken together, these results support the view that ANK2 haploinsufficiency in patients may impair neural development, resulting in an increased risk of ASD. Our study findings provide new insights into the molecular and cellular pathogenesis of ASD, given that among high-confidence ASD genes, ANK2 is rare in that it encodes for a scaffolding protein for the membrane protein complex required for neuronal functions.

摘要

自闭症谱系障碍(ASD)是一种神经发育疾病,其特征为社交沟通改变、兴趣受限和刻板行为。尽管ASD的分子和细胞发病机制仍不清楚,但有研究表明,在皮质发育过程中神经干细胞分化和神经元迁移受损与ASD密切相关。ANK2编码一种细胞骨架支架蛋白,参与将膜蛋白募集到特殊膜结构域中,已被确定为一个高可信度的ASD风险基因。然而,ANK2在早期神经发育中的作用仍不清楚。在本研究中,我们利用子宫内电穿孔技术分析了ANK2在发育中小鼠大脑皮质中的作用。我们提供的证据表明,ANK2在胚胎大脑皮质中高度表达,它调节神经干细胞分化和神经元迁移。我们还证明,敲低Ank2会改变神经发育相关基因的表达。综上所述,这些结果支持这样一种观点,即患者ANK2单倍剂量不足可能会损害神经发育,导致ASD风险增加。鉴于在高可信度的ASD基因中,ANK2很罕见,因为它编码神经元功能所需膜蛋白复合物的支架蛋白,我们的研究结果为ASD的分子和细胞发病机制提供了新的见解。

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Autism-associated ANK2 regulates embryonic neurodevelopment.与自闭症相关的ANK2调节胚胎神经发育。
Biochem Biophys Res Commun. 2022 May 21;605:45-50. doi: 10.1016/j.bbrc.2022.03.058. Epub 2022 Mar 12.
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A Mutation in the ANK2 Gene Causing ASD and a Review of the Literature.ANK2基因中的一种突变导致自闭症谱系障碍及文献综述。
Mol Genet Genomic Med. 2025 Mar;13(3):e70083. doi: 10.1002/mgg3.70083.
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Integrated gene expression and alternative splicing analysis in human and mouse models of Rett syndrome.雷特综合征人类和小鼠模型中的综合基因表达与可变剪接分析。
Sci Rep. 2025 Jan 22;15(1):2778. doi: 10.1038/s41598-025-86114-8.
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A Neuron-Like Cellular Model for Severe Tinnitus Associated with Rare Variations in the ANK2 Gene.一种与ANK2基因罕见变异相关的严重耳鸣的类神经元细胞模型。
Mol Neurobiol. 2025 May;62(5):6467-6477. doi: 10.1007/s12035-024-04674-8. Epub 2025 Jan 15.
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Roles of ANK2/ankyrin-B in neurodevelopmental disorders: Isoform functions and implications for autism spectrum disorder and epilepsy.ANK2/锚蛋白B在神经发育障碍中的作用:异构体功能及其对自闭症谱系障碍和癫痫的影响。
Curr Opin Neurobiol. 2025 Feb;90:102938. doi: 10.1016/j.conb.2024.102938. Epub 2024 Dec 3.
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Chronic Ultrasound Prenatal Stress Altered the Brain's Neurochemical Systems in Newborn Rats.慢性超声产前应激改变了新生大鼠大脑的神经化学系统。
Neural Plast. 2024 Feb 13;2024:3829941. doi: 10.1155/2024/3829941. eCollection 2024.
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A multi-ancestry cerebral cortex transcriptome-wide association study identifies genes associated with smoking behaviors.一项多血统大脑皮层转录组全基因组关联研究鉴定出与吸烟行为相关的基因。
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