Singer I I, Rhode S L
J Virol. 1977 Feb;21(2):724-31. doi: 10.1128/JVI.21.2.724-731.1977.
Partial denaturation mapping, restriction endonuclease digestion, and electron microscopy were used to determine which end of the linear duplex replicative-form (RF) DNA molecule contains the origin of RF replication for the parvovirus H-1. This origin was localized within approximately 300 base pairs of the arbitrarily designated right end of the RF DNA, in the EcoRI or HaeII-A fragment. Based on denaturation behavior in formamide, the right end was also found to have a relatively high guanine plus cytosine content, whereas the region adjacent to the left terminus of the RF DNA molecule was adenine plus thymine rich.
采用部分变性图谱法、限制性内切核酸酶消化法和电子显微镜法来确定细小病毒H-1的线性双链复制型(RF)DNA分子的哪一端包含RF复制起点。该起点定位于RF DNA任意指定右端约300个碱基对范围内,位于EcoRI或HaeII-A片段中。根据在甲酰胺中的变性行为,还发现右端的鸟嘌呤加胞嘧啶含量相对较高,而RF DNA分子左末端相邻区域富含腺嘌呤加胸腺嘧啶。