1. Binding of the SARS-CoV-2 envelope E protein to human BRD4 is essential for infection
- Author
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Kendra R. Vann, Arpan Acharya, Suk Min Jang, Catherine Lachance, Mohamad Zandian, Tina A. Holt, Audrey L. Smith, Kabita Pandey, Donald L. Durden, Dalia El-Gamal, Jacques Côté, Siddappa N. Byrareddy, and Tatiana G. Kutateladze
- Subjects
Coronavirus Envelope Proteins ,Protein Domains ,Structural Biology ,SARS-CoV-2 ,COVID-19 ,Humans ,Nuclear Proteins ,Cell Cycle Proteins ,Molecular Biology ,Protein Binding ,Transcription Factors - Abstract
Emerging new variants of SARS-CoV-2 and inevitable acquired drug resistance call for the continued search of new pharmacological targets to fight the potentially fatal infection. Here, we describe the mechanisms by which the E protein of SARS-CoV-2 hijacks the human transcriptional regulator BRD4. We found that SARS-CoV-2 E is acetylated in vivo and co-immunoprecipitates with BRD4 in human cells. Bromodomains (BDs) of BRD4 bind to the C-terminus of the E protein, acetylated by human acetyltransferase p300, whereas the ET domain of BRD4 recognizes the unmodified motif of the E protein. Inhibitors of BRD4 BDs, JQ1 or OTX015, decrease SARS-CoV-2 infectivity in lung bronchial epithelial cells, indicating that the acetyllysine binding function of BDs is necessary for the virus fitness and that BRD4 represents a potential anti-COVID-19 target. Our findings provide insight into molecular mechanisms that contribute to SARS-CoV-2 pathogenesis and shed light on a new strategy to block SARS-CoV-2 infection.
- Published
- 2022