Abstract
Herpesvirus gene expression is dynamic and complex, with distinct complements of viral genes expressed at specific times in different infection contexts. These complex patterns of viral gene expression arise in part from the integration of multiple cellular and viral signals that affect the transcription of viral genes. The use of alternative promoters provides an increased level of control, allowing different promoters to direct the transcription of the same gene in response to distinct temporal and contextual cues. While once considered rare, herpesvirus alternative promoter usage was recently found to be far more pervasive and impactful than previously thought. Here we review several examples of promoter switching in herpesviruses and discuss the functional consequences on the transcriptional and post-transcriptional regulation of viral gene expression.
Highlights
Herpesviruses are large, enveloped viruses with double-stranded DNA genomes
Whereas black lines denote introns. (c) The human cytomegalovirus (HCMV) UL122 and UL123 genes encode the viral transactivators immediate early (IE) proteins IE1 and IE2, which are expressed from four promoters: the distal promoter (Dp), the major immediate early (MIE) promoter (MIEP), and the intronic promoters intronic promoter 1 (iP1) and intronic promoter 2 (iP2)
While Epstein-Barr virus nuclear antigen 1 (EBNA1) expression appears to remain constant during the multiple forms of Epstein-Barr virus (EBV) latency and lytic replication, EBNA1 expression is the result of a complex amalgamation of host and viral transcription factors regulating EBNA1 alternative promoter usage to drive the ongoing transcription of EBNA1 and other EBNA transcripts
Summary
Annu. Rev. Virol. 2021.8:201-218. Downloaded from www.annualreviews.org Access provided by 3.84.134.36 on 01/20/22. See copyright for approved use. The Annual Review of Virology is online at virology.annualreviews.org https://doi.org/10.1146/annurev-virology-091919072841
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