CCTop: An Intuitive, Flexible and Reliable CRISPR/Cas9 Target Prediction Tool

被引:697
作者
Stemmer, Manuel [1 ]
Thumberger, Thomas [1 ]
Keyer, Maria del Sol [1 ]
Wittbrodt, Joachim [1 ]
Mateo, Juan L. [1 ]
机构
[1] Heidelberg Univ, COS, Heidelberg, Germany
来源
PLOS ONE | 2015年 / 10卷 / 04期
基金
欧洲研究理事会;
关键词
GENOME; ZEBRAFISH; MEDAKA; SYSTEM; ENDONUCLEASE; BACTERIA; GENE;
D O I
10.1371/journal.pone.0124633
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Engineering of the CRISPR/Cas9 system has opened a plethora of new opportunities for site-directed mutagenesis and targeted genome modification. Fundamental to this is a stretch of twenty nucleotides at the 5' end of a guide RNA that provides specificity to the bound Cas9 endonuclease. Since a sequence of twenty nucleotides can occur multiple times in a given genome and some mismatches seem to be accepted by the CRISPR/Cas9 complex, an efficient and reliable in silico selection and evaluation of the targeting site is key prerequisite for the experimental success. Here we present the CRISPR/Cas9 target online predictor (CCTop, http://crispr.cos.uni-heidelberg.de) to overcome limitations of already available tools. CCTop provides an intuitive user interface with reasonable default parameters that can easily be tuned by the user. From a given query sequence, CCTop identifies and ranks all candidate sgRNA target sites according to their off-target quality and displays full documentation. CCTop was experimentally validated for gene inactivation, non-homologous end-joining as well as homology directed repair. Thus, CCTop provides the bench biologist with a tool for the rapid and efficient identification of high quality target sites.
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页数:11
相关论文
共 36 条
[1]   Targeted mutagenesis using CRISPR/Cas system in medaka [J].
Ansai, Satoshi ;
Kinoshita, Masato .
BIOLOGY OPEN, 2014, 3 (05) :362-371
[2]   Highly efficient CRISPR/Cas9-mediated knock-in in zebrafish by homology-independent DNA repair [J].
Auer, Thomas O. ;
Duroure, Karine ;
De Cian, Anne ;
Concordet, Jean-Paul ;
Del Bene, Filippo .
GENOME RESEARCH, 2014, 24 (01) :142-153
[3]  
Baena-Lopez L a., 2013, DEVELOPMENT
[4]   CRISPR-Cas Systems in Bacteria and Archaea: Versatile Small RNAs for Adaptive Defense and Regulation [J].
Bhaya, Devaki ;
Davison, Michelle ;
Barrangou, Rodolphe .
ANNUAL REVIEW OF GENETICS, VOL 45, 2011, 45 :273-297
[5]   ALTERING THE GENOME BY HOMOLOGOUS RECOMBINATION [J].
CAPECCHI, MR .
SCIENCE, 1989, 244 (4910) :1288-1292
[6]   Fate Restriction and Multipotency in Retinal Stem Cells [J].
Centanin, Lazaro ;
Hoeckendorf, Burkhard ;
Wittbrodt, Joachim .
CELL STEM CELL, 2011, 9 (06) :553-562
[7]   Efficient genome editing in Caenorhabditis elegans by CRISPR-targeted homologous recombination [J].
Chen, Changchun ;
Fenk, Lorenz A. ;
de Bono, Mario .
NUCLEIC ACIDS RESEARCH, 2013, 41 (20) :e193
[8]  
Cong L., 2013, Multiplex Genome Engineering Using CRISPR/Cas Systems. Science
[9]  
Farboud B, 2015, DRAMATIC ENHANCEMENT
[10]   Ensembl 2014 [J].
Flicek, Paul ;
Amode, M. Ridwan ;
Barrell, Daniel ;
Beal, Kathryn ;
Billis, Konstantinos ;
Brent, Simon ;
Carvalho-Silva, Denise ;
Clapham, Peter ;
Coates, Guy ;
Fitzgerald, Stephen ;
Gil, Laurent ;
Giron, Carlos Garcia ;
Gordon, Leo ;
Hourlier, Thibaut ;
Hunt, Sarah ;
Johnson, Nathan ;
Juettemann, Thomas ;
Kaehaeri, Andreas K. ;
Keenan, Stephen ;
Kulesha, Eugene ;
Martin, Fergal J. ;
Maurel, Thomas ;
McLaren, William M. ;
Murphy, Daniel N. ;
Nag, Rishi ;
Overduin, Bert ;
Pignatelli, Miguel ;
Pritchard, Bethan ;
Pritchard, Emily ;
Riat, Harpreet S. ;
Ruffier, Magali ;
Sheppard, Daniel ;
Taylor, Kieron ;
Thormann, Anja ;
Trevanion, Stephen J. ;
Vullo, Alessandro ;
Wilder, Steven P. ;
Wilson, Mark ;
Zadissa, Amonida ;
Aken, Bronwen L. ;
Birney, Ewan ;
Cunningham, Fiona ;
Harrow, Jennifer ;
Herrero, Javier ;
Hubbard, Tim J. P. ;
Kinsella, Rhoda ;
Muffato, Matthieu ;
Parker, Anne ;
Spudich, Giulietta ;
Yates, Andy .
NUCLEIC ACIDS RESEARCH, 2014, 42 (D1) :D749-D755