首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >EXPRESSION OF TRANSDUCED GENES IN MICE GENERATED BY INFECTING BLASTOCYSTS WITH AVIAN LEUKOSIS VIRUS-BASED RETROVIRAL VECTORS
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EXPRESSION OF TRANSDUCED GENES IN MICE GENERATED BY INFECTING BLASTOCYSTS WITH AVIAN LEUKOSIS VIRUS-BASED RETROVIRAL VECTORS

机译:用基于禽类白血病病毒的逆转录病毒载体感染母细胞产生的小鼠中转基因基因的表达

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Transgenic mouse lines have been developed that express the tv-a receptor under the control of the chicken beta-actin promoter. These mice express the tv-a receptor in most or all tissues and in the early embryo. An avian leukosis virus (ALV)-based retroviral vector system was used for the efficient delivery of genes into preimplantation mouse embryos from these transgenic lines. Experimental animals could be generated quickly and easily by infecting susceptible blastocysts with ALV-based retroviral vectors. Expression of the delivered genes was controlled by either the constitutive viral promoter contained in the long terminal repeat or an internal nonviral tissue-specific promoter. Mating the infected founder chimeric animals produced animals that carry the ALV provirus as a transgene. A subset of the integrated proviruses expressed the chloramphenicol acetyltransferase reporter gene from either the promoter in the long terminal repeat or an internal promoter, which we believe indicates that many of the sites that are accessible to viral DNA insertion in preimplantation embryos are incompatible with expression in older animals. This approach should prove useful for studies on murine cell lineage and development, providing models for studying oncogenesis, and testing gene therapy strategies. [References: 35]
机译:已经开发了在鸡β-肌动蛋白启动子控制下表达tv-a受体的转基因小鼠品系。这些小鼠在大多数或所有组织和早期胚胎中表达tv-a受体。基于禽白血病病毒(ALV)的逆转录病毒载体系统被用于将基因从这些转基因品系有效地递送到植入前小鼠胚胎中。通过使用基于ALV的逆转录病毒载体感染易感的囊胚,可以快速轻松地生成实验动物。递送的基因的表达由长末端重复序列中包含的组成型病毒启动子或内部非病毒组织特异性启动子控制。将感染的始祖嵌合动物交配产生的动物携带ALV前病毒作为转基因。整合的原病毒的一个子集从长末端重复序列的启动子或内部启动子表达氯霉素乙酰基转移酶报告基因,我们认为这表明许多可在植入前胚胎中插入病毒DNA的位点与在表达中不兼容。年长的动物。这种方法应被证明对鼠细胞谱系和发育的研究有用,为研究肿瘤发生提供模型并测试基因治疗策略。 [参考:35]

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