Vidal M, Wrighton C, Eccles S, Burke J, Grosveld F
Laboratory of Gene Structure and Expression, National Institute for Medical Research, Mill Hill, London, U.K.
Biochim Biophys Acta. 1990 Apr 6;1048(2-3):171-7. doi: 10.1016/0167-4781(90)90053-5.
Vectors carrying the origin of replication, ori-P, of the Epstein-Barr virus (EBV) are maintained extrachromosomally in human cells expressing the EBV nuclear antigen 1 (EBNA-1). We have studied the EBV vectors p201 and p292 in which both ori-P and EBNA-1 functions are present using the human cell lines A431 and HeLa. The two lines showed differences in their transfectability by the EBV vectors. Thousands of HeLa transfectants were obtained with either vector and these remained intact as episomes. A431 could only be efficiently transfected with p292 and a high ratio of chromosomal integrations and rearrangements were observed. The vector p292 expressed the EBNA-1 gene more efficiently than p201 and this was found to be associated with a harmful effect on the grown of both HeLa and A431 lines. These results indicate that EBV vectors behave differently, depending on the cell line and that over-expression of EBNA 1 from these vectors may be detrimental to the cells.
携带爱泼斯坦-巴尔病毒(EBV)复制起点ori-P的载体,在表达EBV核抗原1(EBNA-1)的人类细胞中以染色体外形式维持。我们使用人类细胞系A431和HeLa研究了同时具备ori-P和EBNA-1功能的EBV载体p201和p292。这两种细胞系对EBV载体的转染能力存在差异。用任一载体都能获得数千个HeLa转染子,并且这些转染子作为附加体保持完整。A431只能被p292有效转染,并且观察到高比例的染色体整合和重排。载体p292比p201更有效地表达EBNA-1基因,并且发现这与对HeLa和A431细胞系生长的有害影响有关。这些结果表明,EBV载体的行为因细胞系而异,并且这些载体中EBNA 1的过表达可能对细胞有害。