Human Cytomegalovirus miR-US5-2 Downregulation of GAB1 Regulates Cellular Proliferation and UL138 Expression through Modulation of Epidermal Growth Factor Receptor Signaling Pathways
Affiliation
Department of Immunobiology, BIO5 Institute, University of ArizonaIssue Date
2020
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American Society for MicrobiologyCitation
DeJarnette, C., Luna-Tapia, A., Estredge, L. R., & Palmer, G. E. (2020). Dihydrofolate Reductase Is a Valid Target for Antifungal Development in the Human Pathogen Candida albicans. Msphere, 5(3).Journal
mSphereRights
Copyright © 2020 DeJarnette et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Regulation of epidermal growth factor (EGF) receptor (EGFR) signaling is critical for the replication of human cytomegalovirus (HCMV) as well as latency and reactivation in CD34+ hematopoietic progenitor cells. HCMV microRNAs (miRNAs) provide a means to modulate the signaling activated by EGF through targeting com-ponents of the EGFR signaling pathways. Here, we demonstrate that HCMV miR- US5-2 directly downregulates the critical EGFR adaptor protein GAB1 that mediates activation and sustained signaling through the phosphatidylinositol 3-kinase (PI3K) and MEK/extracellular signal-regulated kinase (ERK) pathways and cellular prolifera¬tion in response to EGF. Expression of HCMV UL138 is regulated by the transcription factor early growth response gene 1 (EGR1) downstream of EGFR-induced MEK/ERK signaling. We show that by targeting GAB1 and attenuating MEK/ERK signaling, miR- US5-2 indirectly regulates EGR1 and UL138 expression, which implicates the miRNA in critical regulation of HCMV latency. Copyright © 2020 Hancocket al. This is an open-access article distributed under the terms ofthe Creative Commons Attribution 4.0 International license.Note
Open access journalISSN
2379-5042PubMed ID
32581079Version
Final published versionae974a485f413a2113503eed53cd6c53
10.1128/msphere.00374-20
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Except where otherwise noted, this item's license is described as Copyright © 2020 DeJarnette et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.
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