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Replication Process of the Parvovirus H-1 II. Isolation and Characterization of H-1 Replicative Form DNA

机译:细小病毒H-1的复制过程II。 H-1复制型DNA的分离与鉴定

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摘要

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 × 106 is twice that of the single-stranded virion DNA. H-1 virions contain DNA that is homogeneous and free of complementary strands.
机译:细小病毒H-1在仓鼠胚胎细胞中自主复制。在感染细胞的S期晚期开始了一种称为HA-DNA合成的DNA合成事件,其后的病毒RNA和病毒血凝素的合成取决于该事件(18)。假定HA-DNA代表亲代病毒复制形式DNA(RF DNA)。这项研究描述了H-1 RF DNA的分离和表征,作为对真核细胞中DNA复制的机制和控制的持续研究的一部分。 H-1 RF DNA是包含病毒链及其补体的线性双链体分子。 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,估计鸟嘌呤加胞嘧啶(GC)含量为45.9%。沉降系数为17S。计算出的分子量3.7×10 6 是单链病毒粒子DNA的两倍。 H-1病毒体含有均质且无互补链的DNA。

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