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Transient replication of BPV-1 requires two viral polypeptides encoded by the E1 and E2 open reading frames.

机译:BPV-1的瞬时复制需要两个由E1和E2开放阅读框编码的病毒多肽。

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摘要

Bovine papillomavirus (BPV) DNA is maintained as an episome with a constant copy number in transformed cells and is stably inherited. To study BPV replication we have developed a transient replication assay based on a highly efficient electroporation procedure. Using this assay we have determined that in the context of the viral genome two of the viral open reading frames, E1 and E2, are required for replication. Furthermore we show that when produced from expression vectors in the absence of other viral gene products, the full length E2 transactivator polypeptide and a 72 kd polypeptide encoded by the E1 open reading frame in its entirety, are both necessary and sufficient for replication BPV in C127 cells.
机译:牛乳头瘤病毒(BPV)DNA在转化细胞中保持为具有恒定拷贝数的附加体,并稳定遗传。为了研究BPV复制,我们基于高效电穿孔程序开发了一种瞬时复制测定法。使用该测定法,我们已经确定,在病毒基因组的背景下,复制需要两个病毒开放阅读框E1和E2。此外,我们表明,当在不存在其他病毒基因产物的情况下由表达载体生产时,完整的E2反式激活多肽和E1开放阅读框编码的72 kd多肽对于在C127中复制BPV既必要又充分细胞。

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