经改造的 Cas9 变体可绕过 Keap1 在人体细胞中介导的降解,提高表观基因组编辑效率。

IF 16.6 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jianfeng Chen, Siyuan Su, Adrian Pickar-Oliver, Anna M Chiarella, Quentin Hahn, Dennis Goldfarb, Erica W Cloer, George W Small, Smaran Sivashankar, Dale A Ramsden, Michael B Major, Nathaniel A Hathaway, Charles A Gersbach, Pengda Liu
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引用次数: 0

摘要

作为一种高效便捷的基因组编辑工具,Cas9 已被广泛应用于生物医学研究,并在治疗人类疾病方面进行了评估。目前已经发现了大量 Cas9、dCas9 和其他相关原核生物内切酶的工程变体。然而,由于这些细菌酶并不天然存在于哺乳动物细胞中,人们对哺乳动物宿主是否以及如何识别和调控细菌Cas9蛋白仍然知之甚少。在这里,我们发现 Keap1 是一种哺乳动物内源性 E3 连接酶,它以一种类似于 "ETGE "的降解子依赖方式靶向 Cas9/dCas9/Fanzor 进行泛素化和降解。逃避Keap1识别的Cas9-'ETGE'-like degron突变体在细胞中显示出更强的基因编辑能力。dCas9-'ETGE'-like degron突变体延长了蛋白半衰期和蛋白在染色质上的保留时间,从而提高了CRISPRa和CRISPRi的功效。此外,与Keap1结合的Cas9也会通过与Keap1底物或结合伙伴竞争Keap1的结合而损害Keap1的功能,而工程化的Cas9突变体对Keap1生物学的干扰较小。因此,我们的研究揭示了哺乳动物特异性的 Cas9 调控,并提供了新的 Cas9 设计,它们不仅具有更强的基因调控能力,而且对破坏内源性 Keap1 信号转导的影响最小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Engineered Cas9 variants bypass Keap1-mediated degradation in human cells and enhance epigenome editing efficiency.

As a potent and convenient genome-editing tool, Cas9 has been widely used in biomedical research and evaluated in treating human diseases. Numerous engineered variants of Cas9, dCas9 and other related prokaryotic endonucleases have been identified. However, as these bacterial enzymes are not naturally present in mammalian cells, whether and how bacterial Cas9 proteins are recognized and regulated by mammalian hosts remain poorly understood. Here, we identify Keap1 as a mammalian endogenous E3 ligase that targets Cas9/dCas9/Fanzor for ubiquitination and degradation in an 'ETGE'-like degron-dependent manner. Cas9-'ETGE'-like degron mutants evading Keap1 recognition display enhanced gene editing ability in cells. dCas9-'ETGE'-like degron mutants exert extended protein half-life and protein retention on chromatin, leading to improved CRISPRa and CRISPRi efficacy. Moreover, Cas9 binding to Keap1 also impairs Keap1 function by competing with Keap1 substrates or binding partners for Keap1 binding, while engineered Cas9 mutants show less perturbation of Keap1 biology. Thus, our study reveals a mammalian specific Cas9 regulation and provides new Cas9 designs not only with enhanced gene regulatory capacity but also with minimal effects on disrupting endogenous Keap1 signaling.

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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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