利用 CRISPECTOR2.0 量化等位基因特异性 CRISPR 编辑活性。

IF 16.6 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Guy Assa, Nechama Kalter, Michael Rosenberg, Avigail Beck, Oshry Markovich, Tanya Gontmakher, Ayal Hendel, Zohar Yakhini
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引用次数: 0

摘要

脱靶效应严重阻碍了 CRISPR-Cas 基因组编辑技术的安全高效使用。由于脱靶活性受基因组序列的影响,序列变异的存在导致不同等位基因或个体的靶上和脱靶情况各不相同。然而,目前还没有一种可靠的工具可以量化等位基因背景下的基因组编辑活性。在这里,我们介绍 CRISPECTOR2.0,它是我们之前发布的软件工具 CRISPECTOR 的扩展版本,具有等位基因特异性编辑活性量化选项。CRISPECTOR2.0 通过使用从头样本特异性单核苷酸变异(SNV)检测和基于统计的等位基因调用算法,实现了无参照、等位基因感知、靶上和靶下活性的精确量化。我们展示了 CRISPECTOR2.0 在分析包含多个等位基因的样本和量化等位基因特异性编辑活性方面的功效,使用的数据来自不同的细胞类型,包括原代人类细胞、植物和一个原始的广泛的人类细胞系数据库。我们发现了 SNV 诱导原间隔相邻基序变化,从而导致等位基因特异性编辑的情况。耐人寻味的是,在携带远端 SNV 的区域也观察到了不同的等位基因编辑,这暗示了其他表观遗传因素的参与。我们的发现凸显了等位基因特异性编辑测量的重要性,它是适应高效、准确和安全的个性化基因组编辑的里程碑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantifying allele-specific CRISPR editing activity with CRISPECTOR2.0.

Off-target effects present a significant impediment to the safe and efficient use of CRISPR-Cas genome editing. Since off-target activity is influenced by the genomic sequence, the presence of sequence variants leads to varying on- and off-target profiles among different alleles or individuals. However, a reliable tool that quantifies genome editing activity in an allelic context is not available. Here, we introduce CRISPECTOR2.0, an extended version of our previously published software tool CRISPECTOR, with an allele-specific editing activity quantification option. CRISPECTOR2.0 enables reference-free, allele-aware, precise quantification of on- and off-target activity, by using de novo sample-specific single nucleotide variant (SNV) detection and statistical-based allele-calling algorithms. We demonstrate CRISPECTOR2.0 efficacy in analyzing samples containing multiple alleles and quantifying allele-specific editing activity, using data from diverse cell types, including primary human cells, plants, and an original extensive human cell line database. We identified instances where an SNV induced changes in the protospacer adjacent motif sequence, resulting in allele-specific editing. Intriguingly, differential allelic editing was also observed in regions carrying distal SNVs, hinting at the involvement of additional epigenetic factors. Our findings highlight the importance of allele-specific editing measurement as a milestone in the adaptation of efficient, accurate, and safe personalized genome editing.

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来源期刊
Nucleic Acids Research
Nucleic Acids Research 生物-生化与分子生物学
CiteScore
27.10
自引率
4.70%
发文量
1057
审稿时长
2 months
期刊介绍: Nucleic Acids Research (NAR) is a scientific journal that publishes research on various aspects of nucleic acids and proteins involved in nucleic acid metabolism and interactions. It covers areas such as chemistry and synthetic biology, computational biology, gene regulation, chromatin and epigenetics, genome integrity, repair and replication, genomics, molecular biology, nucleic acid enzymes, RNA, and structural biology. The journal also includes a Survey and Summary section for brief reviews. Additionally, each year, the first issue is dedicated to biological databases, and an issue in July focuses on web-based software resources for the biological community. Nucleic Acids Research is indexed by several services including Abstracts on Hygiene and Communicable Diseases, Animal Breeding Abstracts, Agricultural Engineering Abstracts, Agbiotech News and Information, BIOSIS Previews, CAB Abstracts, and EMBASE.
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