Sato H, Takimoto T, Hatano M, Pagano J S, Raab-Traub N
Department of Virology, Kanazawa University, Japan.
J Gen Virol. 1989 Mar;70 ( Pt 3):717-27. doi: 10.1099/0022-1317-70-3-717.
Epstein-Barr virus (EBV) from a human hybrid epithelial cell line (NPC-KT), derived from the fusion of human adenoidal cells and EBV genome-containing primary nasopharyngeal carcinoma cells (NPC) has both transforming and early antigen (EA)-inducing abilities. EBV DNA from NPC-KT cells was partially digested with TaqI and ligated to the cloning vector pJB8 at the ClaI site. This cosmid library encompassed the whole genomic DNA of the virus except for several kb of the terminal fragments. The identification and location of each of the cloned DNA fragments have been defined by hybridization to blots prepared with B95-8 and NPC-KT virion DNA. Defective heterogeneous restriction enzyme fragments of the viral DNA were not identified in any of the cosmid clones nor detected in hybridizations to virion DNA, which indicates that a single virus population derived from the NPC tissue has both transforming and EA-inducing activities.
源自人腺样细胞与含EB病毒基因组的原发性鼻咽癌细胞(NPC)融合的人杂交上皮细胞系(NPC-KT)中的EB病毒,具有转化能力和诱导早期抗原(EA)的能力。用TaqI对NPC-KT细胞的EB病毒DNA进行部分消化,并在ClaI位点连接到克隆载体pJB8。该黏粒文库包含病毒的整个基因组DNA,但不包括末端片段的几个kb。通过与用B95-8和NPC-KT病毒体DNA制备的印迹杂交,已确定了每个克隆DNA片段的鉴定和定位。在任何黏粒克隆中均未鉴定出病毒DNA的缺陷异源限制性酶切片段,在与病毒体DNA的杂交中也未检测到,这表明源自NPC组织的单一病毒群体具有转化和诱导EA的活性。