REMOVER-PITCh:利用高度复用的 CRISPR-Cas9 进行微组学辅助长程基因替换。

IF 1.5 4区 生物学 Q4 CELL BIOLOGY
Shu Matsuzaki, Tetsushi Sakuma, Takashi Yamamoto
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引用次数: 0

摘要

目前已开发出多种基于 CRISPR-Cas9 的基因编辑技术,包括基因插入和基因替换,并将其应用于疾病的研究和治疗。为了提高基因插入的效率并以各种方式扩展该系统,人们进行了大量研究,但关于基因置换技术的报道相对较少,因此在这方面仍需进一步改进。在此,我们开发了 REMOVER-PITCh 系统,建立了一种高效的长程基因替换方法,并在人类培养细胞的两个基因组位点上证明了它的实用性。REMOVER-PITCh 依赖于称为 PITCh 的微组学辅助基因插入技术和高度复用的 CRISPR-Cas9。首先,我们利用该系统实现了约 20-kb GUSB 基因座的基因替换。其次,通过应用之前建立的基因敲入增强平台 LoAD 系统和 REMOVER-PITCh,我们实现了 ARSB 基因座约 200 kb 长基因区域的替换。我们的 REMOVER-PITCh 系统可以将各种序列分别从基因组中移除和整合到基因组中,这将有助于生成各种疾病和人源化模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
REMOVER-PITCh: microhomology-assisted long-range gene replacement with highly multiplexed CRISPR-Cas9.

A variety of CRISPR-Cas9-based gene editing technologies have been developed, including gene insertion and gene replacement, and applied to the study and treatment of diseases. While numerous studies have been conducted to improve the efficiency of gene insertion and to expand the system in various ways, there have been relatively few reports on gene replacement technology; therefore, further improvements are still needed in this context. Here, we developed the REMOVER-PITCh system to establish an efficient long-range gene replacement method and demonstrated its utility at two genomic loci in human cultured cells. REMOVER-PITCh depends on microhomology-assisted gene insertion technology called PITCh with highly multiplexed CRISPR-Cas9. First, we achieved gene replacement of about 20-kb GUSB locus using this system. Second, by applying the previously established knock-in-enhancing platform, the LoAD system, along with REMOVER-PITCh, we achieved the replacement of a longer gene region of about 200 kb at the ARSB locus. Our REMOVER-PITCh system will make it possible to remove and incorporate a variety of sequences from and into the genome, respectively, which will facilitate the generation of various disease and humanized models.

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来源期刊
CiteScore
3.70
自引率
4.80%
发文量
96
审稿时长
3 months
期刊介绍: In Vitro Cellular & Developmental Biology - Animal is a journal of the Society for In Vitro Biology (SIVB). Original manuscripts reporting results of research in cellular, molecular, and developmental biology that employ or are relevant to organs, tissue, tumors, and cells in vitro will be considered for publication. Topics covered include: Biotechnology; Cell and Tissue Models; Cell Growth/Differentiation/Apoptosis; Cellular Pathology/Virology; Cytokines/Growth Factors/Adhesion Factors; Establishment of Cell Lines; Signal Transduction; Stem Cells; Toxicology/Chemical Carcinogenesis; Product Applications.
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