Allan G J, Inman G J, Parker B D, Rowe D T, Farrell P J
Ludwig Institute for Cancer Research, St Mary's Hospital Medical School, London, U.K.
J Gen Virol. 1992 Jun;73 ( Pt 6):1547-51. doi: 10.1099/0022-1317-73-6-1547.
B lymphoblastoid cell lines immortalized with P3HR1/633 Epstein-Barr virus (EBV), which has a deletion in the EBV nuclear antigen leader protein (EBNA-LP) gene, were transfected with a vector expressing wild-type EBNA-LP. The EBNA-LP transfectants grew out faster under G418 selection than control cells but expression of EBNA-LP made no significant difference to growth rate or saturation density of the resulting established cell lines. When the cells expressing EBNA-LP were allowed to grow to saturation and then diluted in fresh medium they underwent DNA synthesis more rapidly than control cultures.
用P3HR1/633爱泼斯坦-巴尔病毒(EBV)永生化的B淋巴母细胞系,该病毒的EBV核抗原前导蛋白(EBNA-LP)基因存在缺失,用表达野生型EBNA-LP的载体进行转染。在G418选择下,EBNA-LP转染细胞比对照细胞生长得更快,但EBNA-LP的表达对所得稳定细胞系的生长速率或饱和密度没有显著影响。当让表达EBNA-LP的细胞生长至饱和,然后在新鲜培养基中稀释时,它们比对照培养物更快地进行DNA合成。