Single Cas9 nickase induced generation of NRAMP1 knockin cattle with reduced off-target effects

被引:152
作者
Gao, Yuanpeng [1 ,2 ]
Wu, Haibo [1 ,2 ]
Wang, Yongsheng [1 ,2 ]
Liu, Xin [1 ,2 ]
Chen, Linlin [2 ]
Li, Qian [1 ,2 ]
Cui, Chenchen [1 ,2 ]
Liu, Xu [1 ,2 ]
Zhang, Jingcheng [2 ]
Zhang, Yong [1 ,2 ]
机构
[1] Northwest A&F Univ, Coll Vet Med, Yangling 712100, Shaanxi, Peoples R China
[2] Northwest A&F Univ, Key Lab Anim Biotechnol, Minist Agr, Yangling 712100, Shaanxi, Peoples R China
关键词
CRISPR-Cas9; Off-target; Homologous recombination; Chromatin immunoprecipitation sequencing (ChIP-seq); Nickase; Single-strand break; Tuberculosis; BOVIS BCG VACCINATION; ZINC-FINGER TARGETER; DOUBLE-STRAND BREAKS; HOMOLOGOUS RECOMBINATION; GENE; REPAIR; CRISPR-CAS9; SPECIFICITY; NUCLEASES; MUTAGENESIS;
D O I
10.1186/s13059-016-1144-4
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: The CRISPR-Cas9 system is a widely utilized platform for transgenic animal production in various species, although its off-target effects should be addressed. Several applications of this tool have been proposed in model animals but remain insufficient for transgenic livestock production. Results: Here, we report the first application of single Cas9 nickase (Cas9n) to induce gene insertion at a selected locus in cattle. We identify the main binding sites of a catalytically inactive Cas9 (dCas9) protein in bovine fetal fibroblast cells (BFFs) with chromatin immunoprecipitation sequencing (ChIP-seq). Subsequently, we demonstrate that a single Cas9n-induced single-strand break can stimulate the insertion of the natural resistance-associated macrophage protein-1 (NRAMP1) gene with reduced, but still considerable, off-target effects. Through somatic cell nuclear transfer, we finally obtain transgenic cattle with increased resistance to tuberculosis. Conclusions: Our results contribute to the development of CRISPR-Cas9 system for agriculture applications.
引用
收藏
页数:15
相关论文
共 61 条
[1]   Microhomology-based choice of Cas9 nuclease target sites [J].
Bae, Sangsu ;
Kweon, Jiyeon ;
Kim, Heon Seok ;
Kim, Jin-Soo .
NATURE METHODS, 2014, 11 (07) :705-706
[2]   Stable transfection of the bovine NRAMP1 gene into murine RAW264.7 cells:: Effect on Brucella abortus survival [J].
Barthel, R ;
Feng, JW ;
Piedrahita, JA ;
McMurray, DN ;
Templeton, JW ;
Adams, LG .
INFECTION AND IMMUNITY, 2001, 69 (05) :3110-3119
[3]  
Bibikova M, 2002, GENETICS, V161, P1169
[4]   Single-strand break repair and genetic disease [J].
Caldecott, Keith W. .
NATURE REVIEWS GENETICS, 2008, 9 (08) :619-631
[5]   Multiple targeting motifs direct NRAMP1 into lysosomes [J].
Cheng, Xiang ;
Wang, Huayan .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2012, 419 (03) :578-583
[6]   Analysis of off-target effects of CRISPR/Cas-derived RNA-guided endonucleases and nickases [J].
Cho, Seung Woo ;
Kim, Sojung ;
Kim, Yongsub ;
Kweon, Jiyeon ;
Kim, Heon Seok ;
Bae, Sangsu ;
Kim, Jin-Soo .
GENOME RESEARCH, 2014, 24 (01) :132-141
[7]   Multiplex Genome Engineering Using CRISPR/Cas Systems [J].
Cong, Le ;
Ran, F. Ann ;
Cox, David ;
Lin, Shuailiang ;
Barretto, Robert ;
Habib, Naomi ;
Hsu, Patrick D. ;
Wu, Xuebing ;
Jiang, Wenyan ;
Marraffini, Luciano A. ;
Zhang, Feng .
SCIENCE, 2013, 339 (6121) :819-823
[8]   DNA single-strand break repair and spinocerebellar ataxia with axonal neuropathy-1 [J].
El-Khamisy, S. F. ;
Caldecott, K. W. .
NEUROSCIENCE, 2007, 145 (04) :1260-1266
[9]   Mechanism of eukaryotic homologous recombination [J].
Filippo, Joseph San ;
Sung, Patrick ;
Klein, Hannah .
ANNUAL REVIEW OF BIOCHEMISTRY, 2008, 77 :229-257
[10]   Immunology studies in non-human primate models of tuberculosis [J].
Flynn, JoAnne L. ;
Gideon, Hannah P. ;
Mattila, Joshua T. ;
Lin, PhilanaLing .
IMMUNOLOGICAL REVIEWS, 2015, 264 (01) :60-73