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单纯疱疹病毒DNA包装,无明显DNA合成。

Herpes simplex virus DNA packaging without measurable DNA synthesis.

作者信息

Church G A, Dasgupta A, Wilson D W

机构信息

Department of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York 10461, USA.

出版信息

J Virol. 1998 Apr;72(4):2745-51. doi: 10.1128/JVI.72.4.2745-2751.1998.

Abstract

Herpes simplex virus (HSV) type 1 DNA synthesis and packaging occur within the nuclei of infected cells; however, the extent to which the two processes are coupled remains unclear. Correct packaging is thought to be dependent upon DNA debranching or other repair processes, and such events commonly involve new DNA synthesis. Furthermore, the HSV UL15 gene product, essential for packaging, nevertheless localizes to sites of active DNA replication and may link the two events. It has previously been difficult to determine whether packaging requires concomitant DNA synthesis due to the complexity of these processes and of the viral life cycle; however, we have recently described a model system which simplifies the study of HSV assembly. Cells infected with HSV strain tsProt.A accumulate unpackaged capsids at the nonpermissive temperature of 39 degrees C. Following release of the temperature block, these capsids proceed to package viral DNA in a single, synchronous wave. Here we report that, when DNA replication was inhibited prior to release of the temperature block, DNA packaging and later events in viral assembly nevertheless occurred at near-normal levels. We conclude that, under our conditions, HSV DNA packaging does not require detectable levels of DNA synthesis.

摘要

单纯疱疹病毒1型(HSV-1)的DNA合成与包装发生在受感染细胞的细胞核内;然而,这两个过程的耦合程度仍不清楚。正确的包装被认为依赖于DNA去分支或其他修复过程,而这些事件通常涉及新的DNA合成。此外,对包装至关重要的HSV UL15基因产物定位于活跃DNA复制位点,可能将这两个事件联系起来。由于这些过程以及病毒生命周期的复杂性,以前很难确定包装是否需要伴随DNA合成;然而,我们最近描述了一个简化HSV装配研究的模型系统。感染HSV株tsProt.A的细胞在39℃的非允许温度下积累未包装的衣壳。解除温度阻断后,这些衣壳以单一的同步波继续包装病毒DNA。在此我们报告称,在解除温度阻断之前抑制DNA复制时,DNA包装及病毒装配的后续事件仍以接近正常的水平发生。我们得出结论,在我们的条件下,HSV DNA包装不需要可检测水平的DNA合成。

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Herpes simplex virus DNA replication.
Annu Rev Biochem. 1997;66:347-84. doi: 10.1146/annurev.biochem.66.1.347.

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