Allday M J, Sinclair J H, MacGillivray A J, Sang J H
EMBO J. 1985 Nov;4(11):2955-9. doi: 10.1002/j.1460-2075.1985.tb04029.x.
In a search for exogenous promoters which function in cultured Drosophila cells, we have co-transfected a D. melanogaster cell line with an Epstein-Barr virus (EBV) cosmid clone which encodes the Epstein-Barr nuclear antigen (EBNA-1). Here we report that Drosophila cells containing stably integrated copies of EBNA-1 encoding DNA synthesise a polypeptide of mol. wt. identical to that of authentic EBNA-1, which is detectable with EBNA-positive but not EBNA-negative human serum. As in EBV-transformed lymphoblastoid cells, this neo-antigen is associated with the nucleus of transfected cells suggesting that cellular localisation signals which operate in mammalian cells are also recognised in insect cells.
在寻找能在培养的果蝇细胞中起作用的外源启动子时,我们用一个编码爱泼斯坦 - 巴尔核抗原(EBNA - 1)的爱泼斯坦 - 巴尔病毒(EBV)黏粒克隆与一种黑腹果蝇细胞系进行了共转染。在此我们报告,含有稳定整合的EBNA - 1编码DNA拷贝的果蝇细胞合成了一种分子量与真实EBNA - 1相同的多肽,用EBNA阳性但非EBNA阴性的人血清可检测到该多肽。如同在EBV转化的淋巴母细胞中一样,这种新抗原与转染细胞的细胞核相关联,这表明在哺乳动物细胞中起作用的细胞定位信号在昆虫细胞中也能被识别。