由于Chd8在小鼠皮层发育过程中发生的哈普隆缺陷,导致基因表达的细胞类型特异性失调
Kristina M Yim1, Marybeth Baumgartner1, Martina Krenzer1,2
1Department of Genetics, Yale School of Medicine, New Haven, CT 06510, USA.
bioRxiv : the preprint server for biology
|August 26, 2024
概括
失去CHD8功能会破坏发育中的大脑中的基因调节,影响自闭症谱系障碍 (ASD) 风险. 这项研究揭示了小鼠皮质中细胞特异性基因表达变化,影响了前代细胞和神经元.
科学领域:
- 神经科学是一个神经科学.
- 遗传学 遗传学 是一个
- 发展生物学 发展生物学
背景情况:
- 染色体直酶CHD8中的破坏性变异与自闭症谱系障碍 (ASD) 有关.
- CHD8是一种转录调节器,对神经发育至关重要.
- 假设CHD8功能丧失会破坏大脑基因调节网络,导致ASD.
研究的目的:
- 为了研究CHD8发育中的大脑功能丧失的细胞类型特异性转录效应.
- 为了识别野生类型和Chd8突变小鼠的皮质中的失调基因.
主要方法:
- 单细胞和单核RNA测序被用来描述基因表达.
- 基因表达在胚胎和幼年野生类型和Chd8突变小鼠皮层中进行了分析.
主要成果:
- CHD8和其他自闭症风险基因在发育中的小鼠和人类皮质中表现出保存的表达轨迹.
- 在Chd8突变放射性质细胞中,与神经发育障碍,神经元投射,染色质重塑,信号和迁移相关的基因被调节失调.
- 在Chd8突变激发性皮质神经元中,参与突触组织和活动的基因被失调,这表明突触生成受损或成熟延迟.
结论:
- CHD8功能丧失导致发育中的皮质复杂的转录失调.
- 这些调节障碍可能对神经前体和成熟的刺激神经元产生明显的影响.
- 研究结果提供了关于与CHD8.8相关的ASD病因的分子机制的见解.
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