GHR-mutant pig derived from domestic pig and microminipig hybrid zygotes using CRISPR/Cas9 system

• Published in: Molecular biology reports 2023-06, Vol.50 (6), p.5049-5057
• Main Authors: Tanihara, Fuminori, Hirata, Maki, Namula, Zhao, Wittayarat, Manita, Do, Lanh Thi Kim, Lin, Qingyi, Takebayashi, Koki, Hara, Hiromasa, Nagahara, Megumi, Otoi, Takeshige
• Format: Article
• Language: English
• Subjects: Animal Anatomy; Animal Biochemistry; Animal models; Animals; Biomedical and Life Sciences; Biomedical research; CRISPR; CRISPR-Cas Systems - genetics; Electroporation; Embryo transfer; Embryos; Female; Growth hormones; Histology; Hogs; Humans; Life Sciences; Male; Mating; Medical research; Morphology; Mouse models and CRISPR technologies – the state of the art; Mutants; Oocytes; Original Article; Phenotypes; Receptors, Somatotropin - genetics; Swine - genetics; Swine, Miniature; Zygote; Zygotes
• ISSN: 0301-4851; 1573-4978
• DOI: 10.1007/s11033-023-08388-3

Background Pigs are excellent large animal models with several similarities to humans. They provide valuable insights into biomedical research that are otherwise difficult to obtain from rodent models. However, even if miniature pig strains are used, their large stature compared with other experimental animals requires a specific maintenance facility which greatly limits their usage as animal models. Deficiency of growth hormone receptor (GHR) function causes small stature phenotypes. The establishment of miniature pig strains via GHR modification will enhance their usage as animal models. Microminipig is an incredibly small miniature pig strain developed in Japan. In this study, we generated a GHR mutant pig using electroporation-mediated introduction of the CRISPR/Cas9 system into porcine zygotes derived from domestic porcine oocytes and microminipig spermatozoa. Methods and results First, we optimized the efficiency of five guide RNAs (gRNAs) designed to target GHR in zygotes. Embryos that had been electroporated with the optimized gRNAs and Cas9 were then transferred into recipient gilts. After embryo transfer, 10 piglets were delivered, and one carried a biallelic mutation in the GHR target region. The GHR biallelic mutant showed a remarkable growth-retardation phenotype. Furthermore, we obtained F1 pigs derived from the mating of GHR biallelic mutant with wild-type microminipig, and GHR biallelic mutant F2 pigs through sib-mating of F1 pigs. Conclusions We have successfully demonstrated the generation of biallelic GHR-mutant small-stature pigs. Backcrossing of GHR -deficient pig with microminipig will establish the smallest pig strain which can contribute significantly to the field of biomedical research.