发布: 2017年04月05日第7卷第7期 DOI: 10.21769/BioProtoc.2211 浏览次数: 22177
评审: Longping Victor TseRajesh B. ThippeshappaAnonymous reviewer(s)
Abstract
The programmable Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-associated nuclease 9 (Cas9) technology revolutionized genome editing by providing an efficient way to cut the genome at a desired location (Ledford, 2015). In mammalian cells, DNA lesions trigger the error-prone non-homologous end joining (NHEJ) DNA repair mechanism. However, in presence of a DNA repair template, Homology-Directed Repair (HDR) can occur leading to precise repair of the lesion site. This last process can be exploited to enable precise knock-in changes by introducing the desired genomic alteration on the repair template. In this protocol we describe the delivery of long repair templates (> 200 nucleotides) using recombinant Adeno Associated Virus (rAAV) for CRISPR-Cas9-based knock-in of a C-terminal tag sequence in a human cell line.
Keywords: CRISPR-Cas9 (CRISPR-Cas9)Background
Despite numerous reports on knock-out model systems generated by CRISPR-Cas9, knock-in reports are still lagging behind. Because of the many applications, generating knock-in cell lines remains an obvious goal of genome editing. The introduction of knock-in alterations generally relies on the presence of a repair template DNA and activation of the HDR repair mechanism after a site-specific double strand (ds)DNA break is introduced in the genome close to the site of alteration. Different templates can be delivered to the repair machinery ranging from a classical linearized vector containing extensive homology regions and an optional selection cassette, to single strand (ss)DNA oligonucleotides of about 200 nucleotides (Chen et al., 2011). Although ssDNA oligonucleotides are a popular tool, they can only be used to introduce small alterations such as mutations or epitope tags because of DNA synthesis limitations. In addition, the lack of a selection cassette requires robust screening strategies to identify correct clones as no selective pressure is applied on the HDR process. Successful use of integration-deficient rAAV for homologous recombination was already shown before the availability of tailored nucleases (Khan et al., 2011). Both its efficient delivery and ssDNA genome make rAAV a powerful tool to deliver donor repair templates for homologous recombination. Moreover, the secondary structures at the end of the ssDNA molecule block exonuclease activity and stabilize the donor DNA. Even without the use of specific nucleases, knock-in efficiencies of up to 0.7% were obtained in fibroblasts cells (Russell and Hirata, 1998), which was further increased by introducing selection cassettes.
By combining CRISPR-Cas9 with rAAV-mediated repair template delivery, knock-in cell lines can be generated in a robust manner with efficiencies well beyond 50% when selection cassettes are used. This protocol describes the complete procedure for epitope tagging of a gene of choice in the HCT116 colon carcinoma cell line using CRISPR-Cas9 and rAAV. A timeline for the complete experimental procedure is shown in Figure 1.
Figure 1. Timeline for the generation of a knock-in cell line using CRISPR-Cas9 and rAAV-assisted repair template delivery. Dotted timespans indicate periods of incubation or expansion, requiring limited to no hands-on time.
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文章信息
版权信息
© 2017 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Vandemoortele, G., De Sutter, D. and Eyckerman, S. (2017). Robust Generation of Knock-in Cell Lines Using CRISPR-Cas9 and rAAV-assisted Repair Template Delivery. Bio-protocol 7(7): e2211. DOI: 10.21769/BioProtoc.2211.
分类
分子生物学 > DNA > 诱/突变
分子生物学 > DNA > DNA 重组
细胞生物学 > 细胞工程 > CRISPR-cas9
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