维普中文期刊产品整合服务
3篇 您的检索式:作者名="S.Prather"
    题名 作者 年代 出处 被引量
1Use of gene-editing technology to introduce targeted modifications in pigs显示文摘Pigs are an important resource in agriculture and serve as a model for human diseases. Due to their physiological and anatomical similarities with humans, pigs can recapitulate symptoms of human diseases, making them a useful model in biomedicine. However, in the past pig models have not been widely used partially because of the difficulty in genetic modification. The lack of true embryonic stem cells in pigs forced researchers to utilize genetic modification in somatic cells and somatic cell nuclear transfer(SCNT) to generate genetically engineered(GE) pigs carrying site-specific modifications. Although possible, this approach is extremely inefficient and GE pigs born through this method often presented developmental defects associated with the cloning process. Advancement in the gene-editing systems such as Zinc-Finger Nucleases(ZFNs), Transcription activator-like effector nucleases(TALENs), and the Clustered regularly interspaced short palindromic repeat(CRISPR)/CRISPR-associated 9(Cas9) system have dramatically increased the efficiency of producing GE pigs. These gene-editing systems, specifically engineered endonucleases, are based on inducing double-stranded breaks(DSBs) at a specific location, and then site-specific modifications can be introduced through one of the two DNA repair pathways: non-homologous end joining(NHEJ) or homology direct repair(HDR).Random insertions or deletions(indels) can be introduced through NHEJ and specific nucleotide sequences can be introduced through HDR, if donor DNA is provided. Use of these engineered endonucleases provides a higher success in genetic modifications, multiallelic modification of the genome, and an opportunity to introduce site-specific modifications during embryogenesis, thus bypassing the need of SCNT in GE pig production. This review will provide a historical prospective of GE pig production and examples of how the gene-editing system, led by engineered endonucleases, have improved GE pig production. We wil also present some of our current progress related to the optimal use of CRISPR/Cas9 system during embryogenesis.Junghyun Ryu Randall S.Prather Kiho Lee 2018Journal of Animal Science and Biotechnology2018,9,2:3
2Gene targeting with zinc finger nucleases to produce cloned eGFP knockout pigs显示文摘Jeffrey J.Whyte JianguoZhao Kevin D.Wells Melissa S.Samuel Kristin M.Whitworth Eric M.Walters M. HaroldLaughlin Randall S.Prather 2011Mol Reprod Dev2011,,1:1
3Gene targeting with zinc finger nucleases to produce cloned eGFP knockout pigs显示文摘Jeffrey J.Whyte JianguoZhao Kevin D.Wells Melissa S.Samuel Kristin M.Whitworth Eric M.Walters M. HaroldLaughlin Randall S.Prather 2011Mol. Reprod. Dev2011,,1:1
返回顶部 每页显示:
共1页 首页 上一页 第1页 下一页 末页 /1 跳转

网站首页 | 关于我们 | 联系我们 | 产品服务 | 客服中心 | 广告服务 | 版权声明 | 网站联盟 | 友情链接 | 售卡网点

版权所有© 渝B2-20050021-1 渝公网安备 50019002500403号 违法和不良信息举报中心

互联网出版许可证 新出网证(渝)字10号 全国400电话 - 免长途话费