MOLECULAR-BASIS OF LATENCY IN PATHOGENIC HUMAN VIRUSES

被引:143
作者
GARCIABLANCO, MA
CULLEN, BR
机构
[1] DUKE UNIV, MED CTR, HOWARD HUGHES MED INST, DURHAM, NC 27710 USA
[2] DUKE UNIV, MED CTR, GENET SECT, DURHAM, NC 27710 USA
[3] DUKE UNIV, MED CTR, DEPT MICROBIOL & IMMUNOL, DURHAM, NC 27710 USA
[4] DUKE UNIV, MED CTR, DEPT MED, DURHAM, NC 27710 USA
[5] DUKE UNIV, MED CTR, CELL GROWTH REGULAT & ONCOGENESIS SECT, DURHAM, NC 27710 USA
关键词
D O I
10.1126/science.1658933
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Several human viruses are able to latently infect specific target cell populations in vivo. Analysis of the replication cycles of herpes simplex virus, Epstein-Barr virus, and human immunodeficiency virus suggests that the latent infections established by these human pathogens primarily result from a lack of host factors critical for the expression of viral early gene products. The subsequent activation of specific cellular transcription factors in response to extracellular stimuli can induce the expression of these viral regulatory proteins and lead to a burst of lytic viral replication. Latency in these eukaryotic viruses therefore contrasts with latency in bacteriophage, which is maintained primarily by the expression of virally encoded repressors of lytic replication.
引用
收藏
页码:815 / 820
页数:6
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