Polack A, Hartl G, Zimber U, Freese U K, Laux G, Takaki K, Hohn B, Gissmann L, Bornkamm G W
Gene. 1984 Mar;27(3):279-88. doi: 10.1016/0378-1119(84)90072-6.
DNA of the transforming, nondefective Epstein-Barr virus (EBV) strain M-ABA, which is derived from nasopharyngeal carcinoma cells, was cloned as large overlapping pieces into the cosmid pHC79 . The termini were cloned from closed circular virus DNA molecules out of M-ABA cell DNA in phage lambda L47 . The large overlapping clones were used to prepare a library of subclones with inserts of 1-15 kb. A detailed restriction enzyme map of M-ABA virus DNA reveals the close similarity to isolates from other sources. The high number of tandem repeats in EBV DNA stresses the importance of using cloning vectors that can be propagated in recA- Escherichia coli hosts.
源自鼻咽癌细胞的具有转化能力的非缺陷型爱泼斯坦-巴尔病毒(EBV)毒株M-ABA的DNA,被作为大的重叠片段克隆到黏粒载体pHC79中。其末端是从M-ABA细胞DNA中的闭合环状病毒DNA分子在噬菌体λL47中克隆得到的。这些大的重叠克隆用于构建插入片段大小为1 - 15 kb的亚克隆文库。M-ABA病毒DNA的详细限制性酶切图谱显示其与其他来源的分离株非常相似。EBV DNA中大量的串联重复序列凸显了使用能够在recA -大肠杆菌宿主中繁殖的克隆载体的重要性。