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大鼠染色体免疫干扰素基因的克隆与表达

Cloning and expression of the chromosomal immune interferon gene of the rat.

作者信息

Dijkema R, van der Meide P H, Pouwels P H, Caspers M, Dubbeld M, Schellekens H

出版信息

EMBO J. 1985 Mar;4(3):761-7. doi: 10.1002/j.1460-2075.1985.tb03694.x.

Abstract

The chromosomal immune interferon gene of the rat (IFN-gamma) was identified by screening a recombinant rat lambda phage library with a human IFN-gamma cDNA probe. In contrast to the genes of other rat IFNs, this rat IFN-gamma chromosomal gene contains introns and its structural organization closely resembles that of the human and murine IFN-gamma genes. The rat IFN-gamma gene encodes a signal sequence of 19 amino acids followed by the mature IFN-gamma protein of 137 amino acids. The gene was expressed under control of the simian virus 40 (SV40) early promoter in Chinese hamster ovary (CHO) cells deficient in dihydrofolate reductase (DHFR) after co-transformation with a plasmid containing the mouse DHFR gene. Initial transformants with a DHFR+ phenotype produced IFN-gamma titres ranging from 20 to 1600 units/ml. After stepwise increases in the concentration of methotrexate (MTX) in the growth medium of transformed CHO cells, MTX-resistant clones producing 80 000-100 000 units per ml were isolated. Protein analysis of supernatants of these MTX-resistant cells by polyacrylamide gel electrophoresis revealed a product with an apparent mol. wt. of 18 000 daltons which was not detectable in the growth medium of DHFR+ transformants that did not produce IFN. The product was identified as rat IFN-gamma and constituted approximately 5% of the proteins excreted from these cells.

摘要

通过用人γ-干扰素cDNA探针筛选重组大鼠λ噬菌体文库,鉴定出大鼠的染色体免疫干扰素基因(IFN-γ)。与其他大鼠干扰素基因不同,该大鼠IFN-γ染色体基因含有内含子,其结构组织与人和小鼠的IFN-γ基因非常相似。大鼠IFN-γ基因编码一个由19个氨基酸组成的信号序列,其后是由137个氨基酸组成的成熟IFN-γ蛋白。在用含有小鼠二氢叶酸还原酶(DHFR)基因的质粒共转化后,该基因在缺乏二氢叶酸还原酶(DHFR)的中国仓鼠卵巢(CHO)细胞中,在猿猴病毒40(SV40)早期启动子的控制下表达。具有DHFR+表型的初始转化体产生的IFN-γ滴度范围为20至1600单位/毫升。在转化的CHO细胞生长培养基中逐步增加甲氨蝶呤(MTX)的浓度后,分离出每毫升产生80000-100000单位的MTX抗性克隆。通过聚丙烯酰胺凝胶电泳对这些MTX抗性细胞的上清液进行蛋白质分析,发现一种表观分子量为18000道尔顿的产物,在不产生IFN的DHFR+转化体的生长培养基中无法检测到。该产物被鉴定为大鼠IFN-γ,约占这些细胞分泌蛋白总量的5%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d76/554253/ae9949595b39/emboj00268-0186-a.jpg

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