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将DNA静脉注射到怀孕小鼠体内后子代中的基因转移与表达。

Gene transfer and expression in progeny after intravenous DNA injection into pregnant mice.

作者信息

Tsukamoto M, Ochiya T, Yoshida S, Sugimura T, Terada M

机构信息

Genetics Division, National Cancer Center Research Institute, Tokyo, Japan.

出版信息

Nat Genet. 1995 Mar;9(3):243-8. doi: 10.1038/ng0395-243.

Abstract

Several methods that enable foreign genes to be transferred directly into germ cells and adult animals have been developed, which have stimulated great interest in manipulating genes in vivo. However, there have been no methods available for introducing genes into fetuses. We report here that a single intravenous injection of expression plasmid: lipopolyamine complexes into pregnant mice resulted in successful gene transfer into the embryos. The transgenes thus introduced were expressed in the fetuses and newborn progeny. This simple and new method of gene transfer into embryos will facilitate rapid analysis of transgene effects in the fetuses and will be useful for studying gene-deficient animal models to gain transgene functions at desired stages of embryogenesis.

摘要

已经开发出几种能够将外源基因直接导入生殖细胞和成年动物的方法,这激发了人们对体内基因操作的极大兴趣。然而,目前还没有将基因导入胎儿的方法。我们在此报告,向怀孕小鼠单次静脉注射表达质粒:脂多胺复合物可成功地将基因导入胚胎。这样导入的转基因在胎儿和新生后代中表达。这种将基因导入胚胎的简单新方法将有助于快速分析转基因在胎儿中的作用,并将有助于研究基因缺陷动物模型,以便在胚胎发育的期望阶段获得转基因功能。

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