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Production of Transgenic Chickens Constitutively Expressing Human Erythropoietin (hEPO): Problems with Uncontrollable Overexpression of hEPO Gene

机译:组成型表达人类促红细胞生成素(hEPO)的转基因鸡的生产:hEPO基因无法控制的过表达问题

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The chicken is a promising candidate as a bioreactor for the economical mass production of human therapeutic proteins. Here, we report the successful generation of transgenic chickens that produce high concentrations of human erythropoietin (hEPO) in the blood. Using a Moloney murine leukemia virus (MoMLV)-based pseudotyped retrovirus vector packaged with vesicular stomatitis virus G glycoprotein (VSV-G), the hEPO gene under the control of cytomegalovirus (CMV) promoter was introduced to the blastoderm of freshly laid chicken eggs (stage X). Out of 200 injected eggs, 12 chicks were hatched after 21 days of incubation, and all of the G(0) hatched chicks expressed the vector-encoded hEPO gene. One of the G0 roosters successfully transmitted the hEPO gene to its G(1) progeny by crossing with non-transgenic hens. The concentration of hEPO protein in the chicken blood serum was as high as 90 mu g/mL. Although humans and chickens belong to different classes of the phylogenetic tree, human EPO caused devastating problems in transgenic chickens, including sudden death, polycythemia, vasodilation, and so on, which may be due to the uncontrolled constitutive expression of exogenous protein in the chicken body. Despite many disorders, however, we were able to generate chicks of G(2) generation sired by a rooster of G(1) generation confirming successful establishment of a new line of transgenic chicken characterized by high expression of the hEPO gene. With these chickens, we believe that studies on the evaluating the possibilities of the transgenic animal-mediated bio-pharming and on the hEPO-induced physiological side effects will be greatly facilitated.
机译:鸡是有希望的候选物,可以作为经济生产人类治疗性蛋白质的生物反应器。在这里,我们报告成功产生了在血液中产生高浓度人促红细胞生成素(hEPO)的转基因鸡。使用包装了水泡性口炎病毒G糖蛋白(VSV-G)的基于莫洛尼氏鼠白血病病毒(MoMLV)的假型逆转录病毒载体,将在巨细胞病毒(CMV)启动子控制下的hEPO基因导入刚产下的鸡蛋胚盘中( X阶段)。在孵化21天后,从200个注射的卵中孵化出12只小鸡,所有G(0)孵化的小鸡都表达了载体编码的hEPO基因。其中一位G0雄鸡通过与非转基因母鸡杂交,成功地将hEPO基因传递给其G(1)后代。鸡血清中hEPO蛋白的浓度高达90μg / mL。尽管人和鸡属于不同种类的系统发育树,但人EPO导致转基因鸡遭受毁灭性问题,包括猝死,红细胞增多症,血管舒张等,这可能是由于鸡体内外源蛋白的组成型表达不受控制。尽管有许多疾病,但是,我们能够产生G(1)代雄鸡所生的G(2)代雏鸡,从而证实成功建立了以hEPO基因高表达为特征的新转基因鸡品系。对于这些鸡,我们相信将大大促进有关评估转基因动物介导的生物制药的可能性以及hEPO诱导的生理副作用的研究。

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