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在病毒基因组背景下对卡波西肉瘤相关病毒/人类疱疹病毒8型裂解性复制起点的评估。

Evaluation of the lytic origins of replication of Kaposi's sarcoma-associated virus/human herpesvirus 8 in the context of the viral genome.

作者信息

Xu Yiyang, Rodriguez-Huete Alicia, Pari Gregory S

机构信息

University of Nevada, Reno, Department of Microbiology, 1664 North Virginia Street, Howard Bldg. 210, Reno, NV 89557, USA.

出版信息

J Virol. 2006 Oct;80(19):9905-9. doi: 10.1128/JVI.01004-06.

Abstract

The lytic origins of DNA replication for human herpesvirus 8 (HHV8), oriLyt-L and oriLyt-R, are located between open reading frames K4.2 and K5 and ORF69 and vFLIP, respectively. These lytic origins were elucidated using a transient replication assay. Although this assay is a powerful tool for identifying many herpesvirus lytic origins, it is limited in its ability to evaluate the activity of replication origins in the context of the viral genome. To this end, we investigated the ability of a recombinant HHV8 bacterial artificial chromosome (BAC) to replicate in the absence of oriLyt-R, oriLyt-L, or both oriLyt regions. We generated the HHV8 BAC recombinants (BAC36-DeltaOri-R, BAC36-DeltaOri-L, and BAC36-DeltaOri-RL), which removed one or all of the identified lytic origins. An evaluation of these recombinant BACs revealed that oriLyt-L was sufficient to propagate the viral genome, whereas oriLyt-R alone failed to direct the amplification of viral DNA.

摘要

人类疱疹病毒8型(HHV8)的DNA复制裂解起始位点oriLyt-L和oriLyt-R分别位于开放阅读框K4.2与K5之间以及开放阅读框69(ORF69)与病毒FLICE抑制蛋白(vFLIP)之间。这些裂解起始位点是通过瞬时复制分析得以阐明的。尽管该分析是鉴定许多疱疹病毒裂解起始位点的有力工具,但其在评估病毒基因组背景下复制起始位点活性的能力方面存在局限性。为此,我们研究了重组HHV8细菌人工染色体(BAC)在缺失oriLyt-R、oriLyt-L或两个oriLyt区域的情况下进行复制的能力。我们构建了HHV8 BAC重组体(BAC36-DeltaOri-R、BAC36-DeltaOri-L和BAC36-DeltaOri-RL),它们去除了一个或所有已鉴定的裂解起始位点。对这些重组BAC的评估显示,oriLyt-L足以使病毒基因组得以传播,而单独的oriLyt-R无法指导病毒DNA的扩增。

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