Earticle

현재 위치 Home

Poster Presentation : Transgenesis / Xenotransplatation

Production of Knock-in Embryo by TALEN or CRISPR/Cas9-Mediated Homologous Recombination to Produce Bovine Lactoferrin on Bovine β-Casein Gene Locus

첫 페이지 보기
  • 발행기관
    한국동물생명공학회(구 한국동물번식학회) 바로가기
  • 간행물
    발생공학 국제심포지엄 및 학술대회 바로가기
  • 통권
    The 17th International Symposium on Developmental Biotechnology (2017.10)바로가기
  • 페이지
    pp.155-155
  • 저자
    Da Som Park, Se Eun Kim, Deog-Bon Koo, Man-Jong Kang
  • 언어
    영어(ENG)
  • URL
    https://www.earticle.net/Article/A347407

원문정보

초록

영어
The production of pharmaceutical proteins by transgenic animals is one of the major successes of biotechnology. Knock-in system is a more powerful method to produce mammary gland bioreactor. To date, zinc-finger nuclease(ZFNs), transcription activator- like effector nuclease(TALENs), and clustered regularly interspaced short palindromic repeats(CRISPR)/Cas9 systems have been developed for gene targeting. The objective of this study was to develop a knock-in embryo for expression of bovine lactoferrin in the bovine β-casein gene locus by microinjection of knock-in vector with TALEN or CRISPR/Cas9 into bovine zygote. The three kinds of replacement knock-in vectors containing a different length of homologous arm were constructed. These targeting vectors were used enhanced green fluorescent protein(eGFP) as a positive selection marker. These knock-in vectors with TALEN or CRISPR/Cas9 were microinjected into the pronuclear bovine embryo treated cytochalasin B. And the embryos were cultured to blastocyst in the culture medium. These blastocysts were analyzed by PCR to confirm gene targeting by homologous recombination. As a result, when bLF_1kbHR_GFP knock-in vector with TALEN was microinjected into cytoplasm of bovine zygotes, the efficiency of gene targeting was 11.1-14.3%. Also, when bLF_1kbHR and 40HR_GFP knock-in vector with CRISPR/Cas9 was microinjected into cytoplasm of bovine zygotes, the efficiency of gene targeting was 22.2-26.7% but gene targeting by homologous recombination was not detected when bLF_100HR_GFP knock-in vector was microinjected into cytoplasm of bovine zygotes. The precise bovine lactoferrin gene integration of knock-in embryos was confirmed by DNA sequencing analysis. Our knock-in system may help to create transgenic dairy cattle expressing enhanced bovine lactoferrin protein in the mammary gland via the endogenous expression system of the bovine β-casein gene.

키워드

Knock-in Lactoferrin Bovine β-casein Embryo Microinjection

저자

  • Da Som Park [ Departmentof Animal Science, Chonnam National University, Republic of Korea ]
  • Se Eun Kim [ Departmentof Animal Science, Chonnam National University, Republic of Korea ]
  • Deog-Bon Koo [ Department of Biotechnology, Daegu University, Republic of Korea ]
  • Man-Jong Kang [ Departmentof Animal Science, Chonnam National University, Republic of Korea ]

참고문헌

자료제공 : 네이버학술정보

간행물 정보

발행기관

  • 발행기관명
    한국동물생명공학회(구 한국동물번식학회) [The Korean Society of Animal Reproduction and Biotechnology]
  • 설립연도
    1976
  • 분야
    농수해양>축산학
  • 소개
    동물번식생리학, 동물생명공학, 수의학, 인공수정 및 수정란이식을 이용한 동물개량에 관한 이론과 기술의 발전을 통해 학계, 연구계, 산업계 및 양축가 상호간의 협력을 도모함으로써 동물과학발전 및 사회일반의 이익에 기여 한다는 목적을 위해 노력해 나가겠습니다.

간행물

  • 간행물명
    발생공학 국제심포지엄 및 학술대회 [International Symposium on Developmental Biotechnology]
  • 간기
    연간
  • 수록기간
    2004~2018
  • 십진분류
    KDC 527 DDC 636

이 권호 내 다른 논문 / 발생공학 국제심포지엄 및 학술대회 The 17th International Symposium on Developmental Biotechnology

    피인용수 : 0(자료제공 : 네이버학술정보)

    함께 이용한 논문 이 논문을 다운로드한 분들이 이용한 다른 논문입니다.

      페이지 저장