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细小病毒H-1的复制过程。II. H-1复制型DNA的分离与特性分析。

Replication process of the parvovirus H-1. II. Isolation and characterization of H-1 replicative form DNA.

作者信息

Rhode S L

出版信息

J Virol. 1974 Feb;13(2):400-10. doi: 10.1128/JVI.13.2.400-410.1974.

Abstract

The Parvovirus H-1 replicates autonomously in hamster embryo cells. A DNA synthetic event, called HA-DNA synthesis, upon which subsequent viral RNA and viral hemagglutinin synthesis is dependent, is initiated in late S phase of the infected cell (18). It was postulated that HA-DNA represents parental viral replicative form DNA (RF DNA). This study describes the isolation and characterization of H-1 RF DNA as part of the continuing study of the mechanisms and control of DNA replication in the eukaryotic cell. The H-1 RF DNA is a linear duplex molecule containing the viral strand and its complement. The complementary strands of the RF DNA have been separated by equilibrium density gradient centrifugation. The RF DNA has a buoyant density of 1.705 in neutral CsCl and an estimated guanine plus cytosine (GC) content of 45.9%. It has a sedimentation coefficient of 17S. The calculated molecular weight of 3.7 x 10(6) is twice that of the single-stranded virion DNA. H-1 virions contain DNA that is homogeneous and free of complementary strands.

摘要

细小病毒H-1在仓鼠胚胎细胞中自主复制。一种名为HA-DNA合成的DNA合成事件在受感染细胞的S期后期启动,随后的病毒RNA和病毒血凝素合成依赖于此事件(18)。据推测,HA-DNA代表亲本病毒复制型DNA(RF DNA)。本研究描述了H-1 RF DNA的分离和特性,作为对真核细胞中DNA复制机制和调控持续研究的一部分。H-1 RF DNA是一种线性双链分子,包含病毒链及其互补链。RF DNA的互补链已通过平衡密度梯度离心分离。RF DNA在中性CsCl中的浮力密度为1.705,鸟嘌呤加胞嘧啶(GC)含量估计为45.9%。它的沉降系数为17S。计算出的分子量为3.7 x 10(6),是单链病毒粒子DNA的两倍。H-1病毒粒子含有均匀且不含互补链的DNA。

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