C9orf72的重复扩张破坏了核细胞质运输
Ke Zhang1, Christopher J Donnelly2, Aaron R Haeusler3
1Department of Neurology, School of Medicine, Johns Hopkins University.
Nature
|August 27, 2015
概括
在C9orf72的GGGGCC重复扩张导致ALS和FTD. 研究人员发现,通过向重复RNA来修复核细胞质运输缺陷,可以治疗这些神经退行性疾病.
科学领域:
- 神经科学
- 遗传学
- 分子生物学
背景情况:
- C9orf72 六核酸重复扩张 (HRE) 是肌缩侧面硬化 (ALS) 和前性痴呆 (FTD) 的主要遗传原因.
- 之前的研究表明涉及HRE RNA的有毒功能增益机制,RanGAP1被确定为潜在的相互作用者.
研究的目的:
- 调查核细胞质运输在C9orf72相关的神经退化中的作用.
- 确定与C9orf72突变相关的ALS和FTD的治疗点.
主要方法:
- 在Drosophila的基因查中,RanGAP被确定为HRE诱导的神经退行症的抑制剂.
- 研究了HRERNA和RanGAP之间的相互作用.
- 在HRE表达的,患者衍生的神经元和大脑组织中检查核细胞质运输.
- 测试的小分子和反意义的寡核化物用于拯救运输缺陷.
主要成果:
- 在模型中,RanGAP是一种核细胞质运输调节剂,抑制HRE介导的神经退行.
- RanGAP与HRERNA进行物理相互作用,并且在模型和患者衍生细胞/组织中显示出错位.
- 通过准HRE G四重复器来挽救一个赤字.
结论:
- 核细胞质运输缺陷是C9orf72ALS和FTD的主要致病途径.
- 针对这些传输缺陷为这些破坏性神经退行性疾病提供了一个有前途的药物治疗策略.
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