MicroRNA miR-324-3p induces promoter-mediated expression of RelA gene
Open accessAbstract
MicroRNAs (miRNAs) are known to repress translation by binding to the 3'UTRs of mRNAs. Using bioinformatics, we recently reported that several miRNAs also have target sites in DNA particularly in the promoters of the protein-coding genes. To understand the functional significance of this phenomenon, we tested the effects of miR-324-3p binding to RelA promoter. In PC12 cells, co-transfection with premiR-324-3p induced a RelA promoter plasmid in a dose-dependent manner and this effect was lost when the miR-324-3p binding site in the promoter was mutated. PremiR-324-3p transfection also significantly induced the endogenous RelA mRNA and protein expression in PC12 cells. Furthermore, transfection with premiR-324-3p increased the levels of cleaved caspase-3 which is a marker of apoptosis. Importantly, the miR-324-3p effects were Ago2 mediated as Ago2 knockdown prevented RelA expression and cleavage of caspase-3. Thus, our studies show that miRNA-mediated transcriptional activation can be seen in PC12 cells which are neural in origin.
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miRNA interaction with promoter region has been reported to induce transcription.
“while miRNA interaction with promoter region has been reported to induce transcription (45).”
From Overview of MicroRNA Biogenesis, Mechanisms of Actions, and Circulation (2018) · cites this paper as [45]
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Self-citation
- Authors
- Dharap, A., Pokrzywa, C., Murali, S., Pandi, G., & Vemuganti, R.
- Affiliations
- University of Wisconsin System (US)
- University of Wisconsin–Madison (US)
- Corresponding author
- Vemuganti, Raghu
- Venue
- PLoS ONE
- Publisher
- Public Library of Science (PLoS)
- Published
- 2013-11-12
- Volume
- 8
- Issue
- 11
- Pages
- e79467
- ISSN
- 1932-6203 (ISSN-L)
- PMC
- PMC3827167
- OpenAlex
- W2085865585
- Cited by
- 154
- References
- 25
- Citations by year
- 2026: 7 · 2025: 22 · 2024: 25 · 2023: 20 · 2022: 18 · 2021: 19 · 2020: 18 · 2019: 5 · 2018: 7 · 2017: 3 · 2016: 2 · 2015: 4 · 2014: 4
- FWCI
- 1.17
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- PLoS ONE (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- American Heart Association
- National Institutes of Health
- National Institute of Neurological Disorders and Stroke (NS061071, R03NS067274, NS067274, NS074444, R21NS061071, R21NS074444)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
- Keywords
- miR-324-3p, microRNA, RelA, NF-κB p65, promoter binding, transcriptional activation, Argonaute 2, caspase-3, apoptosis, PC12 cells, neural cells, microRNA binding sites
- MeSH terms
- Animals, Base Sequence, Membrane Proteins, Promoter Regions, Genetic, RNA, Messenger, Transcriptional Activation, Eukaryotic Initiation Factor-2, PC12 Cells, MicroRNAs, Rats, Transcription Factor RelA, Argonaute Proteins
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