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sgRNAcas9:一个用于设计CRISPR sgRNA和评估潜在脱靶切割位点的软件包。

sgRNAcas9: a software package for designing CRISPR sgRNA and evaluating potential off-target cleavage sites.

作者信息

Xie Shengsong, Shen Bin, Zhang Chaobao, Huang Xingxu, Zhang Yonglian

机构信息

Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.

MOE Key Laboratory of Model Animal for Disease Study, Model Animal Research Center of Nanjing University, Nanjing, China.

出版信息

PLoS One. 2014 Jun 23;9(6):e100448. doi: 10.1371/journal.pone.0100448. eCollection 2014.

Abstract

Although the CRISPR/Cas9/sgRNA system efficiently cleaves intracellular DNA at desired target sites, major concerns remain on potential "off-target" cleavage that may occur throughout the whole genome. In order to improve CRISPR-Cas9 specificity for targeted genome editing and transcriptional control, we describe a bioinformatics tool "sgRNAcas9", which is a software package developed for fast design of CRISPR sgRNA with minimized off-target effects. This package consists of programs to perform a search for CRISPR target sites (protospacers) with user-defined parameters, predict genome-wide Cas9 potential off-target cleavage sites (POT), classify the POT into three categories, batch-design oligonucleotides for constructing 20-nt (nucleotides) or truncated sgRNA expression vectors, extract desired length nucleotide sequences flanking the on- or off-target cleavage sites for designing PCR primer pairs to validate the mutations by T7E1 cleavage assay. Importantly, by identifying potential off-target sites in silico, the sgRNAcas9 allows the selection of more specific target sites and aids the identification of bona fide off-target sites, significantly facilitating the design of sgRNA for genome editing applications. sgRNAcas9 software package is publicly available at BiooTools website (www.biootools.com) under the terms of the GNU General Public License.

摘要

尽管CRISPR/Cas9/sgRNA系统能够在所需靶位点高效切割细胞内DNA,但对于可能在整个基因组中发生的潜在“脱靶”切割仍存在重大担忧。为了提高CRISPR-Cas9在靶向基因组编辑和转录控制方面的特异性,我们描述了一种生物信息学工具“sgRNAcas9”,它是一个软件开发包,用于快速设计具有最小脱靶效应的CRISPR sgRNA。该软件包包含多个程序,可使用用户定义的参数搜索CRISPR靶位点(原间隔序列)、预测全基因组范围内Cas9潜在脱靶切割位点(POT)、将POT分为三类、批量设计用于构建20个核苷酸(nt)或截短的sgRNA表达载体的寡核苷酸、提取位于靶上或靶外切割位点侧翼的所需长度核苷酸序列,以设计PCR引物对,通过T7E1切割试验验证突变。重要的是,通过在计算机上识别潜在的脱靶位点,sgRNAcas9允许选择更特异的靶位点,并有助于识别真正的脱靶位点,显著促进用于基因组编辑应用的sgRNA设计。sgRNAcas9软件包可根据GNU通用公共许可证条款在BiooTools网站(www.biootools.com)上公开获取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42ae/4067335/1c416c12291d/pone.0100448.g001.jpg

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