通过CRISPR/Cas9进行体内基因组编辑
Keiichiro Suzuki1, Yuji Tsunekawa2, Reyna Hernandez-Benitez1,3
1Gene Expression Laboratory, Salk Institute for Biological Studies, 10010 N. Torrey Pines Rd, La Jolla, California 92037, USA.
Nature
|November 17, 2016
概括
科学家们开发了一种新的基因编辑方法, 这种基于CRISPR/Cas9的工具可以有效地将DNA整合到各种细胞中,从而促进遗传疾病的基因疗法.
科学领域:
- 生物医学研究
- 基因治疗
- 遗传学
背景情况:
- 工程核酶在生物医学研究中具有临床应用的潜力.
- 目前的活体向转基因整合方法效率低下,特别是在非分裂细胞中,阻碍了遗传疾病的研究和治疗.
研究的目的:
- 开发一种新的,高效的用于分化和非分化细胞中的向DNA整合的方法,用于体外和体内应用.
- 在临床前模型中展示新方法的治疗潜力.
主要方法:
- 基于CRISPR/Cas9技术的同类独立目标集成策略 (HITI) 的开发.
- 在体外和体内测试HITI对DNA敲门的有效性,包括在产后哺乳动物的神经元中.
- 在视网膜色素炎的老鼠模型中评估HITI,以评估其改善视觉功能的治疗潜力.
主要成果:
- 在分裂和不分裂的细胞中,HITI策略可实现强大的DNA敲击.
- 在产后哺乳动物的神经元中成功应用HITI.
- 在使用HITI的视网膜色素炎小鼠模型中显示出视觉功能的改善,显示出治疗效果.
结论:
- 该方法提供了针对性DNA整合的强大和高效方法,克服了现有技术的局限性.
- 这一战略为基础生物学研究和针对遗传疾病的基因治疗开发开辟了新的可能性.
- 在临床前的视网膜退化模型中,HITI是一个有前途的治疗工具.
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