Epstein–Barr virus super-enhancer eRNAs are essential for MYC oncogene expression and lymphoblast proliferation
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Significance: EBV infection causes African Burkitt's lymphoma; Hodgkin's disease; lymphomas in immune suppressed people, including HIV infected people; nasopharyngeal carcinoma; and ∼10% of gastric carcinomas. We recently found EBV super-enhancer (ESE) to be critical for lymphoblastoid cell (LCL) growth and survival. We now identified an ESE constituent, enhancer RNA (eRNA), that is important for ESE function. These eRNAs were activated by viral transactivator, EBV nuclear antigen 2 (EBNA2). MYC oncogene ESE eRNAs were able to enhance ESE activation of MYC expression and are essential for LCL growth. Targeting ESE eRNAs may lead to new therapeutics for EBV-associated malignancies.
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Knockdown of selected enhancer RNAs reduces expression of the corresponding gene targets, suggesting functionality.
“However, studies that knock down selected eRNA have found reduced expression of the corresponding gene targets, suggesting functionality [79–81].”
From Transcriptional enhancers and their communication with gene promoters (2021) · cites this paper as [79]
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Transcriptional enhancers and their communication with gene promoters
Ray-Jones, H., & Spivakov, M. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-03903-w · Cited by 81 · see citing works
- Authors
- Liang, J., Zhou, H., Gerdt, C., Tan, M., Colson, T., Kaye, K. M., Kieff, E., & Zhao, B.
- Affiliations
- Brigham and Women's Hospital (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2016-11-18
- Volume
- 113
- Issue
- 49
- Pages
- 14121-14126
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC5150416
- OpenAlex
- W2556468356
- Cited by
- 88
- References
- 2
- Citations by year
- 2025: 7 · 2024: 7 · 2023: 12 · 2022: 11 · 2021: 18 · 2020: 11 · 2019: 7 · 2018: 6 · 2017: 9
- FWCI
- 3.81
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
- Funders
- HHS | NIH | National Cancer Institute (R01CA047006, R01CA085180, R01CA170023)
- HHS | NIH | National Institute of Allergy and Infectious Diseases (R01AI123420)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Health Sciences › Medicine › Oncology › Viral-associated cancers and disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer-related molecular mechanisms research
- Keywords
- Epstein-Barr virus, super-enhancers, enhancer RNA, MYC oncogene, lymphoblastoid cell lines, EBNA2, BRD4, enhancer looping, H3K27ac, cell proliferation, transcription start sites, chromatin looping
- MeSH terms
- Bromodomain Containing Proteins, Cell Line, Endonucleases, Enhancer Elements, Genetic, Herpesvirus 4, Human, Humans, Lymphoproliferative Disorders, Nuclear Proteins, Transcription Factors, Proto-Oncogene Proteins c-myc, Cell Cycle Proteins, Host-Pathogen Interactions
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