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Whole genome sequencing of a germline transmitted calf

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한국동물생명공학회(구 한국수정란이식학회) (Journal of Animal Reproduction & Biotechnology)
초록

Recently, we published a microinjection method for generating transgenic cattle using the DNA transposon system and their analysis by next-generation sequencing (Yum et al. Sci Rep. 2016 Jun 21;6:27185). In that study, we generated transgenic cattle using two different types of DNA transposon system, sleeping beauty (SB) and piggybac (PB), carrying Yellow fluorescent protein with SB (SB-YFP, female) and green fluorescent protein with PB (PB-GFP, male) under the control of the ubiquitous CAG promoter, respectively. The female and male founder cattle have been grown up to date (the female age: 40 months old, the male age: 33 months old) without any health issues. In genomic instability and blood analysis, there was no significant differences between wild type and founder cattle. In the present study, we confirmed germ-line transmission of the transposon-mediated transgene integrations and ubiquitous and persistent expression of transgene in second generation of offspring (F1). The F1 was born without any assistance and expressed GFP in the eyes without UV light. The ubiquitous expression of GFP was detected in skin fibroblast from the ear tissue and confirmed by genomic DNA PCR, which suggest that the transgene from the PB-GFP was successfully transmitted. Unfortunately, no transgene from SB-YFP were identified. To confirm the transgene integration site, the genomic DNA from blood was extracted and performed next-generation sequencing (NGS). The GFP gene was integrated in chromosome 4 (two copies), and 6. As results, a total of two copies of paternal transgene transmitted into the F1. All the integrated position was not related with coding region and there was no significant difference in genomic variants between transgenic and non-transgenic cattle. To our knowledge, this is the first report of germ-line transmission through non-viral transgenic founder cattle. Those transgenic cattle will be valuable resource to many fields of biomedical research and agricultural science.

저자
  • Soo-Young Yum(Laboratory of Theriogenology and Biotechnology, Department of veterinary clinical science, College of Veterinary Medicine and the Research Institute of Veterinary Science, Seoul National University)
  • Woo-Jae Choi(Laboratory of Theriogenology and Biotechnology, Department of veterinary clinical science, College of Veterinary Medicine and the Research Institute of Veterinary Science, Seoul National University)
  • Ji-Hyun Lee(Laboratory of Theriogenology and Biotechnology, Department of veterinary clinical science, College of Veterinary Medicine and the Research Institute of Veterinary Science, Seoul National University)
  • Choong-Il Lee(Laboratory of Theriogenology and Biotechnology, Department of veterinary clinical science, College of Veterinary Medicine and the Research Institute of Veterinary Science, Seoul National University)
  • Yun-Kyong Jin(Laboratory of Theriogenology and Biotechnology, Department of veterinary clinical science, College of Veterinary Medicine and the Research Institute of Veterinary Science, Seoul National University)
  • Hee-Soo Kim(Theragen BiO Institute, TheragenEtex)
  • Song-Jeon Lee(Theragen BiO Institute, TheragenEtex)
  • Sin-Gi Park(Embryo Research Center, Seoul Dairy Cooperative)
  • In-Gang Shin(Embryo Research Center, Seoul Dairy Cooperative)
  • Hyeong-Jong Kim(Embryo Research Center, Seoul Dairy Cooperative)
  • Seong-Jin Kim(Embryo Research Center, Seoul Dairy Cooperative)
  • Goo Jang(Laboratory of Theriogenology and Biotechnology, Department of veterinary clinical science, College of Veterinary Medicine and the Research Institute of Veterinary Science, Seoul National University)