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细小病毒H-1的复制过程。VIII. H-1复制型DNA复制起点的部分变性图谱绘制及电子显微镜定位

Replication process of the parvovirus H-1. VIII. Partial denaturation mapping and localization of the replication origin of H-1 replicative-form DNA with electron microscopy.

作者信息

Singer I I, Rhode S L

出版信息

J Virol. 1977 Feb;21(2):724-31. doi: 10.1128/JVI.21.2.724-731.1977.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8472/353874/5e9b27824d88/jvirol00206-0298-a.jpg

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