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人类促红细胞生成素基因:在稳定转染的哺乳动物细胞中的高水平表达及染色体定位

Human erythropoietin gene: high level expression in stably transfected mammalian cells and chromosome localization.

作者信息

Powell J S, Berkner K L, Lebo R V, Adamson J W

出版信息

Proc Natl Acad Sci U S A. 1986 Sep;83(17):6465-9. doi: 10.1073/pnas.83.17.6465.

Abstract

The glycoprotein hormone erythropoietin plays a major role in regulating erythropoiesis and deficiencies of erythropoietin result in anemia. Detailed studies of the hormone and attempts at replacement therapy have been difficult due to the scarcity of purified material. We used a cloned human erythropoietin gene to develop stably transfected mammalian cell lines that secrete large amounts of the hormone with potent biological activity. These cell lines were produced by cotransfection of mammalian cells with a plasmid containing a selectable marker and plasmid constructions containing a cloned human erythropoietin gene inserted next to a strong promoter. The protein secreted by these cells stimulated the proliferation and differentiation of erythroid progenitor cells and, with increased selection, several of these cell lines secrete up to 80 mg of the protein per liter of supernatant. Hybridization analysis of DNA from human chromosomes isolated by high resolution dual laser sorting provides evidence that the gene for human erythropoietin is located on human chromosome 7.

摘要

糖蛋白激素促红细胞生成素在调节红细胞生成中起主要作用,促红细胞生成素缺乏会导致贫血。由于纯化材料稀缺,对该激素的详细研究及替代疗法的尝试一直很困难。我们利用克隆的人类促红细胞生成素基因开发了稳定转染的哺乳动物细胞系,这些细胞系能分泌大量具有强大生物活性的激素。这些细胞系是通过将哺乳动物细胞与含有选择标记的质粒以及含有克隆的人类促红细胞生成素基因且该基因插入强启动子旁边的质粒构建体共转染产生的。这些细胞分泌的蛋白质刺激了红系祖细胞的增殖和分化,并且随着筛选的增加,其中一些细胞系每升上清液可分泌多达80毫克的该蛋白质。通过高分辨率双激光分选分离的人类染色体DNA的杂交分析提供了证据,表明人类促红细胞生成素基因位于人类7号染色体上。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8db/386524/c9ddd7a9d4c3/pnas00321-0244-a.jpg

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