Targeted mutagenesis in chicken using CRISPR/Cas9 system

被引:149
|
作者
Oishi, Isao [1 ]
Yoshii, Kyoko [1 ]
Miyahara, Daichi [2 ]
Kagami, Hiroshi [2 ]
Tagami, Takahiro [3 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Biomed Res Inst, 1-8-31 Midorioka, Ikeda, Osaka 5638577, Japan
[2] Shinshu Univ, Fac Agr, 8304 Minamiminowa, Nagano 3994598, Japan
[3] Natl Agr & Food Res Org, Inst Livestock & Grassland Sci, Anim Breeding & Reprod Res Div, 2 Ikenodai, Tsukuba, Ibaraki 3050901, Japan
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
日本科学技术振兴机构;
关键词
PRIMORDIAL GERM-CELLS; GENOME; GENE; TRANSMISSION; CRISPR-CAS9; INJECTION; KNOCKOUT; TALEN; TRANSGENESIS; GENERATION;
D O I
10.1038/srep23980
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
The CRISPR/Cas9 system is a simple and powerful tool for genome editing in various organisms including livestock animals. However, the system has not been applied to poultry because of the difficulty in accessing their zygotes. Here we report the implementation of CRISPR/Cas9-mediated gene targeting in chickens. Two egg white genes, ovalbumin and ovomucoid, were efficiently (> 90%) mutagenized in cultured chicken primordial germ cells (PGCs) by transfection of circular plasmids encoding Cas9, a single guide RNA, and a gene encoding drug resistance, followed by transient antibiotic selection. We transplanted CRISPR-induced mutant-ovomucoid PGCs into recipient chicken embryos and established three germline chimeric roosters (G0). All of the roosters had donor-derived mutant-ovomucoid spermatozoa, and the two with a high transmission rate of donor-derived gametes produced heterozygous mutant ovomucoid chickens as about half of their donor-derived offspring in the next generation (G1). Furthermore, we generated ovomucoid homozygous mutant offspring (G2) by crossing the G1 mutant chickens. Taken together, these results demonstrate that the CRISPR/Cas9 system is a simple and effective gene-targeting method in chickens.
引用
收藏
页数:10
相关论文
共 50 条
  • [31] Targeted mutagenesis in tetraploid switchgrass (Panicum virgatum L.) using CRISPR/Cas9
    Liu, Yang
    Merrick, Paul
    Zhang, Zhengzhi
    Ji, Chonghui
    Yang, Bing
    Fei, Shui-zhang
    PLANT BIOTECHNOLOGY JOURNAL, 2018, 16 (02) : 381 - 393
  • [32] CRISPR/Cas9 mutagenesis in Volvox carteri
    Ortega-Escalante, Jose A.
    Jasper, Robyn
    Miller, Stephen M.
    PLANT JOURNAL, 2019, 97 (04): : 661 - 672
  • [33] Generation of androgen receptor knockout chicken using CRISPR/Cas9 system
    Lengyel, K.
    Eroglu, I.
    Hellmich, R.
    Sid, H.
    Gahr, M.
    Schusser, B.
    TRANSGENIC RESEARCH, 2020, 29 (04) : 478 - 479
  • [34] Comparison of CRISPR/Cas9 expression constructs for efficient targeted mutagenesis in rice
    Mikami, Masafumi
    Toki, Seiichi
    Endo, Masaki
    PLANT MOLECULAR BIOLOGY, 2015, 88 (06) : 561 - 572
  • [35] Establishment of CRISPR/Cas9 mediated targeted mutagenesis in hop (Humulus lupulus)
    Awasthi, Praveen
    Kocabek, Tomas
    Mishra, Ajay Kumar
    Nath, Vishnu Sukumari
    Shrestha, Ankita
    Matousek, Jaroslav
    PLANT PHYSIOLOGY AND BIOCHEMISTRY, 2021, 160 : 1 - 7
  • [36] Parameters affecting frequency of CRISPR/Cas9 mediated targeted mutagenesis in rice
    Masafumi Mikami
    Seiichi Toki
    Masaki Endo
    Plant Cell Reports, 2015, 34 : 1807 - 1815
  • [37] CRISPR/Cas9 establishment-mediated targeted mutagenesis in Macrobrachium nipponense
    Qiao, Hui
    Jiang, Sufei
    Fu, Hongtuo
    Xiong, Yiwei
    Zhang, Wenyi
    Xu, Lei
    Cheng, Dan
    Wang, Jisheng
    FRONTIERS IN PHYSIOLOGY, 2023, 14
  • [38] Comparison of CRISPR/Cas9 expression constructs for efficient targeted mutagenesis in rice
    Masafumi Mikami
    Seiichi Toki
    Masaki Endo
    Plant Molecular Biology, 2015, 88 : 561 - 572
  • [39] Parameters affecting frequency of CRISPR/Cas9 mediated targeted mutagenesis in rice
    Mikami, Masafumi
    Toki, Seiichi
    Endo, Masaki
    PLANT CELL REPORTS, 2015, 34 (10) : 1807 - 1815
  • [40] Targeted mutagenesis using CRISPR/Cas system in medaka
    Ansai, Satoshi
    Kinoshita, Masato
    BIOLOGY OPEN, 2014, 3 (05): : 362 - 371