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Strategies for controlling CRISPR/Cas9 off-target effects and biological variations in mammalian genome editing experiments

机译:控制CRISPR / CAS9偏离目标效应和哺乳动物基因组编辑实验中的生物变异的策略

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摘要

The CRISPR/Cas9 system has enabled efficient modification of genes in a variety of cellular systems for studying phenotypic effects of genetic perturbations. However, with this technology comes the inherent risk of generating off-target effects (OTEs) in addition to the desired modifications. As such, it can be difficult to conclusively determine that the observed phenotypic changes are in fact due to the intended modification of the target gene and not from random mutations elsewhere in the genome. In addition, biological variations observed within cultured cells or laboratory animals can also confound results and need to be addressed. In this article, we review potential sources of experimental and biological variation as well as propose experimental options to minimize and control OTEs and other variations in CRISPR genome editing experiments for exploratory research applications. Confirmation of on-target KO effect by orthogonal approaches is also discussed.
机译:CRISPR / CAS9系统能够在各种细胞系统中能够有效修饰,用于研究遗传扰动的表型效应。 然而,除了除了所需的修改之外,这种技术还具有生成偏离目标效果(OTES)的固有风险。 因此,很难确定观察到的表型变化实际上是由于靶基因的预期修饰而不是从基因组中其他地方的随机突变。 此外,在培养的细胞或实验动物中观察到的生物变化也可以混淆结果并且需要解决。 在本文中,我们审查了潜在的实验和生物变异来源,以及提出的实验选择,以最小化和控制oTES和其他变化的探索性研究应用程序的CRISPR基因组编辑实验。 还讨论了通过正交方法确认目标KO效应。

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