首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >piggyBac transposition into primordial germ cells is an efficient tool for transgenesis in chickens
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piggyBac transposition into primordial germ cells is an efficient tool for transgenesis in chickens

机译:将piggyBac转座为原始生殖细胞是在鸡中进行转基因的有效工具

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摘要

Transgenic birds embody one of the most potent and exciting research tools in biotechnology for agriculture, medicine, and model animals. To date, retrovirus- or lentivirus-mediated transgenesis has been established in chickens and quail. However, despite having a valid technique for viral transduction to achieve transgenic birds, many obstacles exist for practical applications because of relatively low and variable rates of germ-line transmission and transgenic offspring showing transgene silencing, as well as safety issues related to viral vector use. Thus, the generation of transgenic poultry by nonviral integration is a prerequisite for the introduction of biotechnology to practical applications. Herein, we show that a germ-line-competent chicken primordial germ-cell (PGC) line was established with high efficiency of transmission to offspring and that piggyBac transposition into PGCs improved the efficiency of transgenic chicken production and led to high-level transgene expression. GFP transgene-expressing donor PGC-transferred recipient chickens produced donor-derived progenies, and the germ-line transmission efficiency of donor PGCs was 95.2% on average. Subsequently, half of the donor-derived offspring (52.2%) were transgenic chicks because GFP-expressing donor PGCs, in which a transgene was inserted into one chromosome 20, were heterozygous. In all of the transgenic chickens, GFP expression was constant and strong, regardless of age. Our results demonstrate that piggyBac transposition into the chicken PGC line could be the surest way to generate transgenic chickens safely for practical applications.
机译:转基因鸟类是农业,医学和模型动物生物技术中最有效,最令人兴奋的研究工具之一。迄今为止,已经在鸡和鹌鹑中建立了逆转录病毒或慢病毒介导的转基因。然而,尽管具有有效的病毒转导技术来实现转基因禽类,但由于种系传播和显示转基因沉默的转基因后代相对较低且变化率高以及与使用病毒载体有关的安全性问题,在实际应用中仍然存在许多障碍。因此,通过非病毒整合产生转基因家禽是将生物技术引入实际应用的先决条件。在这里,我们表明,建立了具有生殖能力的鸡原始生殖细胞(PGC)系,可以高效率地传播给后代,并且piggyBac转座到PGC中提高了转基因鸡的生产效率,并导致高水平的转基因表达。表达GFP转基因的供体PGC转移的受体鸡产生了供体衍生的后代,供体PGC的种系传递效率平均为95.2%。随后,一半的供体来源的后代(52.2%)是转基因小鸡,因为表达GFP的供体PGC(其中在一个20号染色体上插入了一个转基因)是杂合的。在所有转基因鸡中,无论年龄大小,GFP的表达都恒定且强。我们的结果表明,将piggyBac转座到鸡PGC品系中可能是安全地生产转基因鸡以用于实际应用的最可靠方法。

著录项

  • 来源
  • 作者

    Tae Sub Park; Jae Yong Han;

  • 作者单位

    World Class University Biomodulation Major, Department of Agricultural Biotechnology, Research Institute for Agriculture and Life Sciences, College of Agriculture and Life Sciences, Seoul National University, Seoul 151-921, Korea;

    World Class University Biomodulation Major, Department of Agricultural Biotechnology, Research Institute for Agriculture and Life Sciences, College of Agriculture and Life Sciences, Seoul National University, Seoul 151-921, Korea;

  • 收录信息 美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    germ-line chimera; piggybac transposon; avian;

    机译:种系嵌合体小猪转座子;禽类;

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