Krysan P J, Calos M P
Department of Genetics, Stanford University School of Medicine, CA 94305.
Gene. 1993 Dec 22;136(1-2):137-43. doi: 10.1016/0378-1119(93)90457-e.
Vectors based on Epstein-Barr virus (EBV) have been useful for cloning and gene expression studies in primate cells. However, these vectors do not replicate in rodent cells. We demonstrate here that the addition of large fragments of mammalian DNA to vectors containing the EBNA-1 gene (encoding the Epstein-Barr nuclear antigen-1) and the family of repeats from EBV generates autonomously replicating vectors which are stably maintained as extrachromosomal plasmids in hamster cells. By using a density-shift assay in Cs2SO4 density gradients, we demonstrate that the plasmids replicate once per cell cycle at high efficiency. These plasmids represent, for rodent cells, the only available class of stable, autonomous vectors replicating once per cell cycle. It is likely that this type of EBV-based autonomous replication system can also be extended to other organisms for which stable, extrachromosomal plasmid systems are not available.
基于爱泼斯坦-巴尔病毒(EBV)的载体已被用于灵长类细胞的克隆和基因表达研究。然而,这些载体在啮齿动物细胞中不能复制。我们在此证明,将大片段哺乳动物DNA添加到含有EBNA-1基因(编码爱泼斯坦-巴尔核抗原-1)和EBV重复序列家族的载体中,可产生自主复制载体,这些载体作为染色体外质粒在仓鼠细胞中稳定维持。通过在Cs2SO4密度梯度中进行密度转移分析,我们证明这些质粒在每个细胞周期高效复制一次。对于啮齿动物细胞而言,这些质粒代表了唯一一类每个细胞周期复制一次的稳定自主载体。这种基于EBV的自主复制系统很可能也能扩展到其他没有稳定染色体外质粒系统的生物体。