# Molecular Switch Regulating Human Cytomegalovirus Replicative and Latent States

> **NIH NIH R01** · UNIVERSITY OF ARIZONA · 2020 · $530,788

## Abstract

SUMMARY
Human cytomegalovirus (HCMV) establishes latent infection in hematopoietic progenitor cells. Differentiation of
latently infected cells induces reactivation of the HCMV lytic cycle, and subsequent viral spread to multiple organs
and tissues. A significant gap in our knowledge is our limited understanding of the mechanisms controlling HCMV
reactivation. Understanding the mechanisms by which HCMV reactivates from latency is critical to developing
new strategies to limit and control life-threatening disease in immune compromised individuals, such as
transplant recipients. A critical step in the establishment of and reactivation from HCMV latency is the expression
of the major immediate early proteins (MIE) IE1 and IE2, which are crucial transactivators of the viral lytic cycle.
During lytic infection, the major immediate early promoter (MIEP) drives the expression of IE1 and IE2 from a
single, alternatively spliced mRNA. During latency, the MIEP is silenced, and IE1 and IE2 are not expressed.
HCMV reactivation induces IE1 and IE2 re-expression, therefore it has been presumed that HCMV reactivation
requires activation of the MIEP to allow for re-expression of IE1 and IE2. However, our preliminary results show
that the MIEP remains silent when latently infected cells are exposed to reactivation stimuli. These data raise
the intriguing question: If the MIEP remains inactive, how does HCMV express MIE transcripts during
reactivation? Through a series of collaborative studies, we find that alternative MIE promoters we recently
identified within the first MIE intron are activated to high levels during reactivation. These transcripts differ from
MIEP-derived transcripts solely in their 5’ untranslated regions due to alternative transcription start site usage.
Importantly, each of the novel transcripts encodes full length IE1 (72-kDa) or IE2 (86-kDa) proteins. Further, our
data show that the novel MIE promoters are necessary for IE1 and IE2 re-expression upon reactivation in
experimental models of HCMV latency, but not during replication in fibroblasts. Further, we have identified
specific host transcription factors (TFs) induced during differentiation that also activate the intronic MIE
promoters. We hypothesize that HCMV reactivation from latency requires activation of novel MIE intronic
promoters by host TFs associated with myeloid differentiation. In Aim 1, we will define the promoter elements
required for IE1 and IE2 re-expression during HCMV reactivation from latency using recombinant viruses in cell
lines and primary human hematopoietic progenitors cells. In Aim 2, we will define the role of specific host factors
required for differentiation-dependent reactivation of IE1/2 in reactivation. Our proposed studies offer exciting
paradigm-shifting insights into the mechanisms that control herpesvirus reactivation. Through collaboration, this
multi-PI study is uniquely positioned to make significant advances in our understanding of herpesvirus
reac...

## Key facts

- **NIH application ID:** 9996481
- **Project number:** 5R01AI143191-03
- **Recipient organization:** UNIVERSITY OF ARIZONA
- **Principal Investigator:** Felicia D Goodrum
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $530,788
- **Award type:** 5
- **Project period:** 2018-09-24 → 2023-08-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/9996481

## Citation

> US National Institutes of Health, RePORTER application 9996481, Molecular Switch Regulating Human Cytomegalovirus Replicative and Latent States (5R01AI143191-03). Retrieved via AI Analytics 2026-06-11 from https://api.ai-analytics.org/grant/nih/9996481. Licensed CC0.

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