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利用CRISPR/Cas9系统构建Tiki1基因修饰猪模型
引用本文:吴彩霞,刘朝明,颜泉梅,张全军,赵宇,欧阳振,樊娜娜,赖良学.利用CRISPR/Cas9系统构建Tiki1基因修饰猪模型[J].生物化学与生物物理进展,2019,46(9):900-908.
作者姓名:吴彩霞  刘朝明  颜泉梅  张全军  赵宇  欧阳振  樊娜娜  赖良学
作者单位:吉林大学动物医学学院,长春 130062;中国科学院广州生物医药与健康研究院,广州 510530,吉林大学动物医学学院,长春 130062;中国科学院广州生物医药与健康研究院,广州 510530,中国科学院广州生物医药与健康研究院,广州 510530,中国科学院广州生物医药与健康研究院,广州 510530,中国科学院广州生物医药与健康研究院,广州 510530,中国科学院广州生物医药与健康研究院,广州 510530,中国科学院广州生物医药与健康研究院,广州 510530,吉林大学动物医学学院,长春 130062;中国科学院广州生物医药与健康研究院,广州 510530
基金项目:国家重点研发计划-神经疾病大动物模型的建立及干细胞治疗评价(2017YFA0105100)和国家重点基础研究发展计划(973)-发育与生殖重要哺乳动物模型的建立(2011CB944200)资助.
摘    要:Tiki1基因是哈佛大学儿童医学院贺熹教授实验室发现的一个对蛙头部的诱导起到决定性作用的新基因,但Tiki1基因在小鼠等啮齿类动物中缺失,因此无法利用小鼠等小动物来研究其在哺乳动物中的作用.本文利用CRISPR/Cas9系统结合体细胞克隆技术构建Tiki1基因修饰猪模型,研究Tiki1基因在猪发育中的作用.我们利用贺熹教授团队提供的人Tiki1基因序列,在猪的基因组数据库中比对出与其同源性最高的一段序列设计2个靶位点(g1和g2).以设计的靶位点构建打靶质粒转染猪胎儿成纤维细胞,经细胞筛选、PCR扩增及测序共鉴定了52个单细胞克隆株.最终选择靶位点g1为纯合双敲的5个单细胞克隆株和靶位点g2为纯合双敲的3个单细胞克隆株作为构建Tiki1基因敲除猪的核供体.我们共计构建了720个重组胚胎,分别植入3头代孕母猪,其中有1头经B超检测成功怀孕并妊娠到期产下13头发育正常的克隆猪,经测序鉴定其中12头为Tiki1基因双敲除猪模型,Tiki1基因敲除克隆猪健康存活至今.结果表明Tiki1基因对于猪早期发育的作用机理不同于蛙,其在猪早期发育的过程中的具体作用机理有待后续进一步的深入研究.

关 键 词:CRISPR/Cas9  Tiki1  基因打靶  猪模型
收稿时间:2018/11/29 0:00:00
修稿时间:2019/6/10 0:00:00

Construction of Tiki1 Gene Modified Pig Model by CRISPR/Cas9 System
WU Cai-Xi,LIU Zhao-Ming,YAN Quan-Mei,ZHANG Quan-Jun,ZHAO Yu,OUYANG Zhen,FAN Na-Na and LAI Liang-Xue.Construction of Tiki1 Gene Modified Pig Model by CRISPR/Cas9 System[J].Progress In Biochemistry and Biophysics,2019,46(9):900-908.
Authors:WU Cai-Xi  LIU Zhao-Ming  YAN Quan-Mei  ZHANG Quan-Jun  ZHAO Yu  OUYANG Zhen  FAN Na-Na and LAI Liang-Xue
Institution:College of Veterinary Medicine, Jilin University, Changchun 130062, China; Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou 510530, China,College of Veterinary Medicine, Jilin University, Changchun 130062, China; Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou 510530, China,Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou 510530, China,Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou 510530, China,Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou 510530, China,Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou 510530, China,Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou 510530, China,College of Veterinary Medicine, Jilin University, Changchun 130062, China; Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou 510530, China
Abstract:Tiki1 gene, found and named by Professor He Xi"s team from Boston Children"s Hospital, Harvard Medical School, plays a key role in the formation of head in Xenopus. However, as Tiki1 gene is absent in rodents such as mice, it is impossible to use mice or rat to study its role in mammals. In this study, we generated Tiki1 gene modified pigs using CRISPR/Cas9 system combined with somatic cell cloning technology to study the role of Tiki1 gene in pig development. Aligned the human Tiki1 mRNA sequence provided by professor He Xi"s team with the pig genome database, we selected two target sites (g1 and g2) with the top 2 highest sequence identity at the predicted pig Tiki1 gene locus. The sgrRNA plasmid was constructed to transfect porcine fetal fibroblasts, and 52 single cell clones were screened and sequenced. We finally selected 5 single-cell clones with biallelic knockout mutations at target site g1 and 3 single-cell clones with biallelic knockout mutations at target site g2 as nuclear donors for constructing Tiki1 knockout pigs. A total of 720 recombinant embryos were constructed and transferred into three surrogate sows and one of them was successfully pregnant monitored by B ultrasound. A total of 13 cloned piglets (ten living piglets and 3 dead piglets ) were produced, and 12 of them were biallelic knockout mutations at Tiki1 locus. Both the living and dead Tiki1 gene knockout cloned piglets were developed normally and the living piglets have survived healthy till now. The results indicate that the role of Tiki1 gene on early development of pigs is different from that of frogs. The specific role of Tiki1 gene in the early development of pigs needs to be further investigated.
Keywords:CRISPR/Cas9  Tiki1  gene targeting  pig model
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