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12型腺病毒的脱氧核糖核酸整合到幼仓鼠肾细胞的脱氧核糖核酸中。

Integration of the deoxyribonucleic acid of adenovirus type 12 into the deoxyribonucleic acid of baby hamster kidney cells.

作者信息

Doerfler W

出版信息

J Virol. 1970 Nov;6(5):652-66. doi: 10.1128/JVI.6.5.652-666.1970.

Abstract

In a previous report, evidence was presented that the deoxyribonucleic acid (DNA) of adenovirus type 12 (Ad12) is integrated by covalent linkage into the DNA of baby hamster kidney cells (BHK-21 cells). These studies have been extended. The DNA of Ad12 and that of BHK-21 cells grown in medium containing 5-bromodeoxyuridine could be separated by equilibrium centrifugation in alkaline CsCl density gradients. BHK-21 cells were infected with (3)H-labeled Ad12, and the total intracellular DNA was analyzed at various times after infection in alkaline CsCl density gradients. The (3)H label in the position of cellular DNA hybridized predominantly with viral DNA and to a lesser extent also with cellular DNA. Replication of viral DNA could not be detected in BHK-21 cells. The appearance of viral (3)H label in the density stratum of cellular DNA was not significantly affected when DNA synthesis in Ad12-infected BHK-21 cells was inhibited >96% by cytosine arabinoside. These findings provided additional evidence for integration of Ad12 DNA into the DNA of BHK-21 cells. It could be calculated that 5 to 55 Ad12 DNA equivalents per cell are integrated. Replication of viral or cellular DNA was not required for integration. Inhibition of protein or ribonucleic acid synthesis interfered with integration only slightly.

摘要

在之前的一份报告中,有证据表明12型腺病毒(Ad12)的脱氧核糖核酸(DNA)通过共价连接整合到幼仓鼠肾细胞(BHK - 21细胞)的DNA中。这些研究已经得到扩展。在含有5 - 溴脱氧尿苷的培养基中培养的Ad12和BHK - 21细胞的DNA,可以通过在碱性CsCl密度梯度中的平衡离心进行分离。用(3)H标记的Ad12感染BHK - 21细胞,并在感染后的不同时间在碱性CsCl密度梯度中分析细胞内的总DNA。细胞DNA位置的(3)H标记主要与病毒DNA杂交,也有较小程度与细胞DNA杂交。在BHK - 21细胞中未检测到病毒DNA的复制。当阿糖胞苷将Ad12感染的BHK - 21细胞中的DNA合成抑制>96%时,病毒(3)H标记在细胞DNA密度层中的出现没有受到显著影响。这些发现为Ad12 DNA整合到BHK - 21细胞的DNA中提供了额外的证据。据计算,每个细胞整合了5到55个Ad12 DNA当量。整合不需要病毒或细胞DNA的复制。蛋白质或核糖核酸合成的抑制对整合仅有轻微干扰。

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