在没有双链断裂或捐赠DNA的情况下进行基因组搜索和替换编辑
Andrew V Anzalone1,2,3, Peyton B Randolph1,2,3, Jessie R Davis1,2,3
1Merkin Institute of Transformative Technologies in Healthcare, Broad Institute of Harvard and MIT, Cambridge, MA, USA.
Nature
|October 22, 2019
概括
主编辑是一种新的基因组编辑技术, 这种多功能工具可以高效地修复大多数引起疾病的变种,
科学领域:
- 分子生物学
- 遗传学
- 生物技术
背景情况:
- 在没有副产品的情况下, 很难有效地纠正基因变异.
- 现有的基因组编辑方法在精度和范围上有局限性.
研究的目的:
- 这是一种多功能且精确的基因组编辑方法.
- 证明原始编辑能够纠正人类细胞中的各种基因突变.
主要方法:
- 主编辑使用了与反转录酶融合的催化受损的Cas9.
- 一个主要编辑指导RNA (pegRNA) 编程系统以准特定的DNA位点并编码编辑.
- 在人类细胞中进行了超过175次编辑, 包括插入,删除和所有12个点突变类型.
主要成果:
- 成功纠正状细胞病和泰萨克斯病的遗传原因.
- 在PRNP中安装了保护性转换,并精确地插入了标签/表位.
- 原始编辑表现出高效率和较少的副产品比同质导向的修复.
- 与标准的Cas9核酶相比,显示了较低的目标外编辑.
结论:
- 主编辑扩展了基因组编辑的能力.
- 这种方法有可能纠正多达89%的已知与疾病相关的遗传变异.
- 提供精确和多功能的基因疾病纠正方法.
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