Nonhuman Primate Genomes Have Limited Relevance for Evaluating Human CRISPR Off-Target Effects.

IF 4.6 3区 医学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Laura Blaha, Mia Bosinger, Dale L Bodian, Victoria Qu, Jason B Warner, Christopher M Borges, Christian Mueller
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Abstract

Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) technology has revolutionized genetic medicine by enabling precise genome editing for therapeutic benefit. CRISPR nucleases are programmed to target genomic sites with sequence complementarity to the spacer region of an associated guide RNA. However, these nucleases may target genomic loci with sequences similar to the target site, which can lead to unintended disruption of off-target genes. The risks associated with these off-target editing events are critical to assess as CRISPR-based in vivo editing systems advance to clinical development. Nonhuman primates (NHPs) are common model species for evaluating the human safety of many therapeutic modalities, but their relevance for evaluating human CRISPR off-target activity has yet to be determined. In this study, 1,220,908 Cas12a and 6,159,066 Cas9 spacer sequences targeting human genes were designed, and off-target editing sites were computationally predicted in humans and five common NHP species. Of the 7,413 Cas12a and 570,754 Cas9 spacers meeting defined on- and off-target inclusion criteria, only 14-21% of Cas12a and 7-15% of Cas9 human off-targets per spacer are recapitulated in the genomes of NHPs commonly used in preclinical studies. These results highlight the limitations of NHPs for the study of human CRISPR spacer specificity and contextualize human risk informed by these studies.

非人类灵长类基因组对评估人类CRISPR脱靶效应的相关性有限。
聚类规则间隔短回文重复序列(CRISPR)技术通过实现精确的基因组编辑以获得治疗益处,彻底改变了遗传医学。CRISPR核酸酶被编程为靶向与相关引导RNA的间隔区序列互补的基因组位点。然而,这些核酸酶可能靶向与目标位点序列相似的基因组位点,这可能导致非目标基因的意外破坏。随着基于crispr的体内编辑系统向临床发展,评估与这些脱靶编辑事件相关的风险至关重要。非人灵长类动物(NHPs)是评估许多治疗方式对人类安全性的常见模型物种,但它们与评估人类CRISPR脱靶活性的相关性尚未确定。在这项研究中,设计了1,220,908个Cas12a和6,159,066个靶向人类基因的Cas9间隔序列,并在人类和5个常见的NHP物种中计算预测了脱靶编辑位点。在符合定义的靶向和脱靶纳入标准的7,413个Cas12a和570,754个Cas9间隔物中,每个间隔物中只有14-21%的Cas12a和7-15%的Cas9人类脱靶在临床前研究中常用的NHPs基因组中被概括。这些结果突出了NHPs在研究人类CRISPR间隔物特异性方面的局限性,并将这些研究提供的人类风险背景化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Human gene therapy
Human gene therapy 医学-生物工程与应用微生物
CiteScore
6.50
自引率
4.80%
发文量
131
审稿时长
4-8 weeks
期刊介绍: Human Gene Therapy is the premier, multidisciplinary journal covering all aspects of gene therapy. The Journal publishes in-depth coverage of DNA, RNA, and cell therapies by delivering the latest breakthroughs in research and technologies. Human Gene Therapy provides a central forum for scientific and clinical information, including ethical, legal, regulatory, social, and commercial issues, which enables the advancement and progress of therapeutic procedures leading to improved patient outcomes, and ultimately, to curing diseases.
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