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비외과적 수정란 이식에 의한 형질전환 소 생산 기술

Production of Transgenic Cattle by Non-surgical Embryo Transfer

  • 엄상준 (상지영서대학교 동물생명산업과) ;
  • 양정석 (상지영서대학교 동물생명산업과) ;
  • 이수민 (상지영서대학교 동물생명산업과) ;
  • 조소영 (상지영서대학교 동물생명산업과) ;
  • 허영태 (충북대학교 축산학과) ;
  • 허영남 (충북대학교 축산학과) ;
  • 구본철 (대구가톨릭대학교 의학과) ;
  • 정기수 (강원도가축위생시험소남부지소) ;
  • 김광재 (강원도가축위생시험소남부지소) ;
  • 김지태 (강원도가축위생시험소남부지소) ;
  • 김남형 (충북대학교 축산학과) ;
  • 고대환 (상지영서대학교 동물생명산업과)
  • Uhm, Sang Jun (Department of Animal Science and Biotechnology, Sangji Youngseo College) ;
  • Yang, Jung Seok (Department of Animal Science and Biotechnology, Sangji Youngseo College) ;
  • Lee, Su Min (Department of Animal Science and Biotechnology, Sangji Youngseo College) ;
  • Joe, So Young (Department of Animal Science and Biotechnology, Sangji Youngseo College) ;
  • Heo, Young-Tae (Department of Animal Sciences, Chungbuk National University) ;
  • Xu, Yong-Nan (Department of Animal Sciences, Chungbuk National University) ;
  • Koo, Bon Chul (Department of Physiology, Catholic University of Daegu School of Medicine) ;
  • Cheong, Ki Soo (South Branch of Gangwondo Veterinary Service LAB) ;
  • Kim, Kwang Jae (South Branch of Gangwondo Veterinary Service LAB) ;
  • Kim, Ji Tae (South Branch of Gangwondo Veterinary Service LAB) ;
  • Kim, Nam-Hyung (Department of Animal Sciences, Chungbuk National University) ;
  • Ko, Dae-Hwan (Department of Animal Science and Biotechnology, Sangji Youngseo College)
  • 투고 : 2013.07.05
  • 심사 : 2013.08.05
  • 발행 : 2013.09.30

초록

Recently, the transgenic animal production technique is very important for the production of bio-parmaceutical as animal bio-reactor system. However, the absence of survival evaluation in vitro produced transgenic embryos has been a problem of the low productivity of transgenic animal because of absent of pre-estimate of pregnancy after transgenic embryos transferred into recipient. Therefore, this study is conducted to improve efficiency of transgenic cattle production by improving the non-surgical embryo transfer (ET) method. Transgenic bovine embryos were produced by injection of feline immunodeficiency virus enhanced green fluorescent protein (FIV-EGFP) lentiviral vector into perivitelline space of in vitro matured MII stage oocytes, and then in vitro fertilization (IVF) was occured. Normal IVF and EGFP expressing blastocysts were transferred into recipients. Results indicated that 2 expanded blastocysts (34.7%) transferred group showed significantly (P<0.05) higher pregnancy rate than 1 expanded blastocyst (26.8%) transferred group. In case of parity of recipient, ET to heifer (34.9%) showed significantly (P<0.05) higher pregnancy rate than ET to multiparous recipient (21.2%). However, there are no significant differences of pregnancy rate between natural induced estrus and artificial induced estrus groups. Significantly (P<0.05) higher pregnancy rate was obtained from recipient group which have normal corpus luteum with crown group (34.8%) than normal corpus luteum without crown (13.6%). Additionally, treatment of $100{\mu}g$ Gn-RH injection to recipient group (38.6%) 1 day before ET significantly (P<0.05) increase pregnancy rate than non- Gn-RH injection to recipient group (38.6%). We also transferred 2 EGFP expressing expanded blastocysts to each 19 recipients, 7 recipients were pregnant and finally 5 EGFP transgenic cattle were produced under described ET condition. Therefore, our result suggested that transfer of 2 good-quality expanded blastocysts to $100{\mu}g$ of Gn-RH injected recipient which have normal corpus luteum with crown is feasible to produce transgenic cattle.

키워드

참고문헌

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