Cited by 154MicroRNA in disease regulationRNA Interference and Gene DeliveryPlant Molecular Biology Research

MicroRNA miR-324-3p induces promoter-mediated expression of RelA gene

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Dharap, Ashutosh, Pokrzywa, Courtney, Murali, Shruthi, Pandi, Gopal, Vemuganti, Raghu·2013·PLoS ONE

Abstract

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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  1. [9]Janowski BA, Younger ST, Hardy DB, Ram R, Huffman KE, et al (2007) Activating gene expression in mammalian cells with promoter-targeted duplex RNAs. Nat Chem Biol 3: 166– 173. 17259978

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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
Published
2013-11-12
Volume
8
Issue
11
Pages
e79467
ISSN
1932-6203 (ISSN-L)
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
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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