Plasmid Partitioning by Human Tumor Viruses

被引:15
|
作者
Chiu, Ya-Fang [1 ,2 ,3 ]
Sugden, Bill [4 ]
机构
[1] Chang Gung Univ, Dept Microbiol & Immunol, Taoyuan, Taiwan
[2] Chang Gung Univ, Res Ctr Emerging Viral Infect, Taoyuan, Taiwan
[3] Linkou Chang Gung Mem Hosp, Dept Med Lab, Taoyuan, Taiwan
[4] Univ Wisconsin, McArdle Lab Canc Res, Madison, WI 53706 USA
基金
美国国家卫生研究院;
关键词
human tumor viruses; partitioning; synthesis; SARCOMA-ASSOCIATED HERPESVIRUS; EPSTEIN-BARR-VIRUS; HUMAN-PAPILLOMAVIRUS TYPE-16; LATENTLY INFECTED-CELLS; NUCLEAR ANTIGEN LANA; KAPOSIS-SARCOMA; DNA-REPLICATION; VIRAL GENOME; TERMINAL REPEAT; STABLE REPLICATION;
D O I
10.1128/JVI.02170-17
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The human tumor viruses that replicate as plasmids (we use the term plasmid to avoid any confusion in the term episome, which was coined to mean DNA elements that occur both extrachromosomally and as integrated forms during their life cycles, as does phage lambda) share many features in their DNA synthesis. We know less about their mechanisms of maintenance in proliferating cells, but these mechanisms must underlie their partitioning to daughter cells. One amazing implication of how these viruses are thought to maintain themselves is that while host chromosomes commit themselves to partitioning in mitosis, these tumor viruses would commit themselves to partitioning before mitosis and probably in S phase shortly after their synthesis.
引用
收藏
页数:8
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