Cradick Thomas J, Qiu Peng, Lee Ciaran M, Fine Eli J, Bao Gang
Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Georgia, USA.
Mol Ther Nucleic Acids. 2014 Dec 2;3(12):e214. doi: 10.1038/mtna.2014.64.
Precise genome editing using engineered nucleases can significantly facilitate biological studies and disease treatment. In particular, clustered regularly interspaced short palindromic repeats (CRISPR) with CRISPR-associated (Cas) proteins are a potentially powerful tool for modifying a genome by targeted cleavage of DNA sequences complementary to designed guide strand RNAs. Although CRISPR/Cas systems can have on-target cleavage rates close to the transfection rates, they may also have relatively high off-target cleavage at similar genomic sites that contain one or more base pair mismatches, and insertions or deletions relative to the guide strand. We have developed a bioinformatics-based tool, COSMID (CRISPR Off-target Sites with Mismatches, Insertions, and Deletions) that searches genomes for potential off-target sites (http://crispr.bme.gatech.edu). Based on the user-supplied guide strand and input parameters, COSMID identifies potential off-target sites with the specified number of mismatched bases and insertions or deletions when compared with the guide strand. For each site, amplification primers optimal for the chosen application are also given as output. This ranked-list of potential off-target sites assists the choice and evaluation of intended target sites, thus helping the design of CRISPR/Cas systems with minimal off-target effects, as well as the identification and quantification of CRISPR/Cas induced off-target cleavage in cells.
使用工程核酸酶进行精确的基因组编辑能够显著促进生物学研究和疾病治疗。特别是,成簇规律间隔短回文重复序列(CRISPR)与CRISPR相关(Cas)蛋白相结合,是一种通过靶向切割与设计的引导链RNA互补的DNA序列来修饰基因组的潜在强大工具。尽管CRISPR/Cas系统的靶向切割率可能接近转染率,但它们在含有一个或多个碱基对错配以及相对于引导链存在插入或缺失的相似基因组位点上,也可能具有相对较高的脱靶切割率。我们开发了一种基于生物信息学的工具COSMID(具有错配、插入和缺失的CRISPR脱靶位点),用于在基因组中搜索潜在的脱靶位点(http://crispr.bme.gatech.edu)。基于用户提供的引导链和输入参数,COSMID能够识别与引导链相比具有指定数量错配碱基以及插入或缺失的潜在脱靶位点。对于每个位点,还会输出适合所选应用的扩增引物。这份潜在脱靶位点的排名列表有助于选择和评估预期的靶位点,从而帮助设计具有最小脱靶效应的CRISPR/Cas系统,以及识别和定量CRISPR/Cas在细胞中诱导的脱靶切割。