Improvement of Porcine SCNT Embryo Development Using Histone Deacetylase Inhibitors

DOI HANDLE オープンアクセス
  • Lee Jin-Hee
    Department of Animal Science and Biotechnology, College of Agriculture and Life Science, Chungnam National University
  • Chun Ju Lan
    Department of Animal Science and Biotechnology, College of Agriculture and Life Science, Chungnam National University
  • Lee Ji Hye
    Department of Animal Science and Biotechnology, College of Agriculture and Life Science, Chungnam National University
  • Kim Keun Jung
    Department of Animal Science and Biotechnology, College of Agriculture and Life Science, Chungnam National University
  • Kim Eun Young
    Department of Animal Science and Biotechnology, College of Agriculture and Life Science, Chungnam National University
  • Han Kil-Woo
    Department of Animal Science and Biotechnology, College of Agriculture and Life Science, Chungnam National University
  • 後藤 貴文
    九州大学大学院農学研究院農学部附属農場高原農業実験実習場
  • Kim Min Kyu
    Department of Animal Science and Biotechnology, College of Agriculture and Life Science, Chungnam National University

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抄録

Somatic cell nuclear transfer (SCNT) has been used in crucial and potential fields of the animal reproduction. Despite the successful birth of cloned animals, the cloning efficiency of SCNT has been still low. Abnormal epigenetic reprogramming has been reported as the cause of the low efficiency of SCNT in cloned embryos. Here, the study aimed to improve the developmental competence of porcine SCNT embryos using Trichostatin A (TSA) and Scriptaid which are well known as histone deacetylase inhibitors that would enhance epigenetic reprograming in cloned embryos by suppressing the event of histone deacetylation. Moreover, this study tested whether Scriptaid would be a substitute for TSA because it has been suggested that TSA is involved in malformation of cloned embryos. Various concentrations of Scriptaid were tested and 500 nM Scriptaid treatment resulted in a significant improvement of the cloned embryo during development regarding the blastocyst formation rates. When cloned embryos were treated with 50 nM TSA or/and 500 nM Scriptaid for 15 h or 24 h, the blastocyst rates of reconstructed embryos were increased in comparison to the untreated control group. However, there was no dose–dependent difference among groups. When donor cells were treated with 50 nM TSA or/and 500 nM Scriptaid for 4 h the blastocyst rates of reconstructed embryos were increased in comparison with the untreated control group. Moreover the expression levels of histone deacetylase 1 (HDAC1) and histone deacetylase 2 (HDAC2) were decreased with TSA and/or Scriptaid treatment. In conclusion, TSA and/or Scriptaid treatments significantly increased the developmental competence of porcine SCNT embryos. In addition, Scriptaid improved the development of SCNT embryos regardless of the TSA treatment. Therefore, Scriptaid would be an alternative additive to improve the development competence of cloned embryos after SCNT.

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詳細情報 詳細情報について

  • CRID
    1390009224684786688
  • NII論文ID
    120005725050
  • NII書誌ID
    AA00247166
  • DOI
    10.5109/1564091
  • HANDLE
    2324/1564091
  • ISSN
    00236152
  • 本文言語コード
    en
  • データソース種別
    • JaLC
    • IRDB
    • Crossref
    • CiNii Articles

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