Ott A, Föhring B, Kaerner H C
J Virol. 1979 Feb;29(2):423-30. doi: 10.1128/JVI.29.2.423-430.1979.
DNA-DNA reassociation kinetics of herpes simplex virus type 1 Angelotti DNA and a class of defective viral DNA revealed that the viral standard genome has a total sequence complexity of about 93 X 10(6) daltons and that a portion of 11 X 10(6) daltons occurs twice on the viral genome. These results agree with structural features of herpes simplex virus type 1 DNA derived from electron microscopic studies and restriction enzyme analyses by several investigators. The defective viral DNA (molecular weight, about 97 X 10(6)) displays a sequence complexity of about 11 X 10(6) daltons, suggesting that the molecule is built up by repetitions of standard DNA sequences comprising about 15,000 base pairs. A 2 X 10(6)-dalton portion of these sequences maps in the redundant region and a 9 X 10(6)-dalton portion maps in the unique part of the standard herpes simplex virus type 1 Angelotti DNA, as could be shown by reassociation of viral standard DNA in the presence of defective DNA and vice versa. No cellular DNA sequences could be detected in defective DNA. A 12% molar fraction of the defective DNA consists of highly repetitive sequences of about 350 to 500 base pairs in length.
1型单纯疱疹病毒安杰洛蒂DNA与一类缺陷病毒DNA的DNA-DNA重缔合动力学研究表明,病毒标准基因组的总序列复杂度约为93×10⁶道尔顿,且11×10⁶道尔顿的一部分在病毒基因组上出现了两次。这些结果与几位研究者通过电子显微镜研究和限制性内切酶分析得出的1型单纯疱疹病毒DNA的结构特征相符。缺陷病毒DNA(分子量约为97×10⁶)的序列复杂度约为11×10⁶道尔顿,这表明该分子是由包含约15,000个碱基对的标准DNA序列重复构建而成的。这些序列中2×10⁶道尔顿的部分定位于冗余区域,9×10⁶道尔顿的部分定位于1型单纯疱疹病毒安杰洛蒂标准DNA的独特部分,这可通过在缺陷DNA存在的情况下病毒标准DNA的重缔合得以证明,反之亦然。在缺陷DNA中未检测到细胞DNA序列。缺陷DNA的12%摩尔分数由长度约为350至500个碱基对的高度重复序列组成。