Temporal dynamics of HCMV gene expression in lytic and latent infections

被引:26
|
作者
Rozman, Batsheva [1 ]
Nachshon, Aharon [1 ]
Samia, Roi Levi [1 ]
Lavi, Michael [1 ]
Schwartz, Michal [1 ]
Stern-Ginossar, Noam [1 ]
机构
[1] Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel
来源
CELL REPORTS | 2022年 / 39卷 / 02期
基金
以色列科学基金会; 欧洲研究理事会;
关键词
HUMAN CYTOMEGALOVIRUS LATENCY; SODIUM-BUTYRATE; LATE TIMES; REACTIVATION; TRANSCRIPTION; REPLICATION; PROTEIN; CELLS; ACTIVATION; SEQUENCE;
D O I
10.1016/j.celrep.2022.110653
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
During productive human cytomegalovirus (HCMV) infection, viral genes are expressed in a coordinated cascade that conventionally relies on the dependencies of viral genes on protein synthesis and viral DNA replication. By contrast, the transcriptional landscape of HCMV latency is poorly understood, Here, we examine viral gene expression dynamics during the establishment of both productive and latent HCMV infections. We redefine HCMV gene expression kinetics during productive infection and reveal that viral gene regulation does not represent a simple sequential cascade; many viral genes are regulated by multiple independent modules. Using our improved gene expression classification combined with transcriptome-wide measurements of the effects of a wide array of epigenetic inhibitors on viral gene expression during latency, we show that a defining feature of latency is the unique repression of immediate-early (IE) genes. Altogether, we recharacterize HCMV gene expression kinetics and reveal governing principles of lytic and latent gene expression.
引用
收藏
页数:18
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