用Cas9和AAV修复模板进行基因组工程,成功和陷
M C Birling1, Y Hérault2,3, G Pavlovic2
1CNRS, INSERM, CELPHEDIA, Institut Clinique de la Souris (ICS), Université de Strasbourg, Illkirch, PHENOMIN, France. birlingm@igbmc.fr.
概括
再组合腺相关病毒 (rAAV) 与CRISPR/Cas9相结合,增强基因组编辑,用于创建动物模型. 这种方法提高了产生精确突变的效率,克服了以前的交付挑战.
科学领域:
- 分子生物学分子生物学
- 遗传学 是一个遗传学.
- 生物技术是生物技术.
背景情况:
- 克里斯普尔/Cas9是产生动物模型的强大工具.
- 为精确的突变提供捐赠者DNA,如敲入,仍然是低效的.
- 再组合腺相关病毒 (rAAV) 为捐赠者DNA输送提供了一个有前途的解决方案.
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