Janik J E, Huston M M, Rose J A
Proc Natl Acad Sci U S A. 1981 Mar;78(3):1925-9. doi: 10.1073/pnas.78.3.1925.
We have used DNA transfection to identify several regions of the adenovirus genome needed to induce replication of the defective parvovirus, adenovirus-associated virus (AAV). Previous studies have indicated that only early adenovirus functions are needed to aid the replication of AAV. In this report, we demonstrate that three restriction endonuclease fragments of adenovirus DNA are necessary for production of infectious AAV in 293-31 cells (an adenovirus type 5-transformed human embryonic kidney cell line). These fragments map from 28.5 to 29.4, 59.5 to 75.9, and 89.7 to 100 map units on the adenovirus type 2 genome and correspond to the locations of the VAI RNA gene, early region 2, and early region 4, respectively. The 293-31 cell line, which has been found to express early region 1A and 1B proteins, alone is incapable of supporting AAV replication or even AAV DNA synthesis. Additional experiments with adenovirus type 5 host range mutants (group I, hr1 and group II, hr7) indicate, however, that early region 1A provides an essential function(s) for AAV replication, whereas early region 1B probably does not.
我们利用DNA转染来鉴定腺病毒基因组中诱导缺陷型细小病毒——腺相关病毒(AAV)复制所需的几个区域。先前的研究表明,仅腺病毒早期功能有助于AAV的复制。在本报告中,我们证明腺病毒DNA的三个限制性内切酶片段对于在293 - 31细胞(一种5型腺病毒转化的人胚肾细胞系)中产生感染性AAV是必需的。这些片段在2型腺病毒基因组上分别位于28.5至29.4、59.5至75.9和89.7至100图距单位处,分别对应于VAI RNA基因、早期区域2和早期区域4的位置。已发现表达早期区域1A和1B蛋白的293 - 31细胞系单独无法支持AAV复制甚至AAV DNA合成。然而,对5型腺病毒宿主范围突变体(I组,hr1和II组,hr7)的进一步实验表明,早期区域1A为AAV复制提供了一种必需功能,而早期区域1B可能并非如此。