Rymo L, Forsblom S
Nucleic Acids Res. 1978 Apr;5(4):1387-402. doi: 10.1093/nar/5.4.1387.
The cleavage of the DNAs of the B95-8 and P3HR-1 virus strains of Epstein-Barr virus by the restriction endonucleases EcoRI, HindIII and BamI was investigated using a new technique for quantitative evaluation of the fluorescence of ethidium stained DNA fragments separated on agarose gels. The results obtained with B95-8 DNA showed that in addition to the limited repetitions of nucleotide sequences observed in the EcoRI and HindIII cleavage patterns, the molecule contained a BamI fragment with a molecular mass of 2.0 megadaltons which was present in a total of about 11 copies and localized to a limited part of the DNA molecule. The same sequences were also present in the P3HR-1 DNA albeit in a lower molar ratio. P3HR-1 DNA yielded restriction enzyme cleavage patterns suggesting DNA sequence heterogeneity of P3HR-1 virus. No fragment was present in more than about 4 copies per molecule of P3HR-1 DNA. Comparison of the restriction enzyme cleavage patterns of P3HR-1 and B95-8 DNA revealed a high degree of structural homology emphasized by nucleic acid hybridization experiments with EBV complementary RNA synthesized in vitro.
采用一种新的技术对在琼脂糖凝胶上分离的经溴化乙锭染色的DNA片段的荧光进行定量评估,研究了限制性内切酶EcoRI、HindIII和BamI对爱泼斯坦-巴尔病毒的B95-8和P3HR-1病毒株DNA的切割情况。用B95-8 DNA得到的结果表明,除了在EcoRI和HindIII切割模式中观察到的核苷酸序列有限重复外,该分子还含有一个分子量为2.0兆道尔顿的BamI片段,总共约有11个拷贝,定位于DNA分子的有限部分。相同的序列也存在于P3HR-1 DNA中,尽管摩尔比更低。P3HR-1 DNA产生的限制性酶切模式表明P3HR-1病毒的DNA序列存在异质性。每分子P3HR-1 DNA中,没有一个片段的拷贝数超过约4个。P3HR-1和B95-8 DNA的限制性酶切模式比较显示,通过用体外合成的EBV互补RNA进行核酸杂交实验,强调了它们高度的结构同源性。