异常拼接在ALS/FTD中使C9ORF72重复扩张变异
Suzhou Yang1,2, Denethi Wijegunawardana1,2, Udit Sheth3,4
1Department of Neuroscience, Yale University School of Medicine, New Haven, CT 06520, USA.
bioRxiv : the preprint server for biology
|November 28, 2023
概括
C9ORF72基因的核酸重复扩张 (NRE) 导致ALS和FTD. 这项研究揭示了NRE触发异常拼接,影响RNA输出和翻译,为这些神经退行性疾病提供了新的见解.
科学领域:
- 遗传学 是一个遗传学.
- 神经科学是一个神经科学.
- 分子生物学分子生物学
背景情况:
- C9ORF72基因核酸重复扩张 (NRE) 是肌缩侧面硬化症 (ALS) 和前性痴呆症 (FTD) 的主要遗传原因.
- 内部NREs影响细胞质翻译机制的机制尚不清楚.
研究的目的:
- 调查C9ORF72基因中的内基NREs是如何从核中处理和出口的.
- 确定异常拼接在C9ORF72相关的ALS和FTD病变发生过程中的作用.
主要方法:
- 从患者衍生细胞中捕获和测序含有NRE的RNA.
- 在患者衍生的运动神经元和人类大脑组织中分析C9ORF72异常拼接.
- 报告员测试评估NRE对密码拼接部位激活的影响.
主要成果:
- 发现C9 NRE通过下游5拼接位的使用而被外化,导致它们从核中以各种拼接的mRNA异型形式出口.
- 在NRE阳性运动神经元和脑组织中,C9ORF72的异常拼接显著增加.
- 病理性的NREs足以激活记者mRNA中的神秘拼接位.
结论:
- 重复诱导的异常拼接在NRE含有RNAs的生物发生,核出口和翻译中发挥着关键作用.
- 异常拼接是将C9ORF72 NREs与ALS和FTD病原体联系起来的关键机制.
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