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将人类珠蛋白基因转移至红白血病小鼠细胞。

Transfer of human globin genes to erythroleukemic mouse cells.

作者信息

Spandidos D A, Paul J

出版信息

EMBO J. 1982;1(1):15-20. doi: 10.1002/j.1460-2075.1982.tb01117.x.

Abstract

Thymidine kinase negative (TK-) Friend cells were transformed with recombinant molecules carrying human globin genes and the thymidine kinase gene of herpes simplex virus type 1 DNA. Transformation frequencies of 1 transformant/microgram donor DNA/1 x 10(6) cells were obtained by standard procedures and this was increased 20- to 30-fold by treating recipient cells with dimethyl sulfoxide or glycerol. Transformed cell lines expressed thymidine kinase activity of viral origin as determined by its insensitivity to 0.2 mM dTTP and electrophoretic mobility in polyacrylamide gels. The physical status of donor DNA in the transformed cells was examined in Hirt precipitates and supernatants by Southern blot hybridization and spot hybridization techniques. This analysis showed that most donor sequences were present in a circular or concatenate configuration, but also was suggestive of some donor sequences being integrated into high molecular weight DNA. Expression of human globin genes and particularly the epsilon-globin gene in the transformed Friend cells was studied by Northern blot hybridization analysis.

摘要

用携带人珠蛋白基因和1型单纯疱疹病毒DNA胸苷激酶基因的重组分子转化胸苷激酶阴性(TK-)弗氏细胞。通过标准程序获得的转化频率为每微克供体DNA/1×10⁶个细胞产生1个转化体,用二甲基亚砜或甘油处理受体细胞可使该频率提高20至30倍。通过对0.2 mM三磷酸胸苷(dTTP)不敏感以及在聚丙烯酰胺凝胶中的电泳迁移率来确定,转化细胞系表达病毒来源的胸苷激酶活性。通过Southern印迹杂交和斑点杂交技术在Hirt沉淀和上清液中检测转化细胞中供体DNA的物理状态。该分析表明,大多数供体序列以环状或串联形式存在,但也提示一些供体序列整合到了高分子量DNA中。通过Northern印迹杂交分析研究了转化的弗氏细胞中人珠蛋白基因尤其是ε-珠蛋白基因的表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb64/552988/bc98024404f8/emboj00293-0025-a.jpg

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