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Evidence for natural antisense transcript-mediated inhibition of microRNA function
Abstract
Background: MicroRNAs (miRNAs) have the potential to regulate diverse sets of mRNA targets. In addition, mammalian genomes contain numerous natural antisense transcripts, most of which appear to be non-protein-coding RNAs (ncRNAs). We have recently identified and characterized a highly conserved non-coding antisense transcript for beta-secretase-1 ( BACE1 ), a critical enzyme in Alzheimer's disease pathophysiology. The BACE1 -antisense transcript is markedly up-regulated in brain samples from Alzheimer's disease patients and promotes the stability of the (sense) BACE1 transcript. Results: We report here that BACE1 -antisense prevents miRNA-induced repression of BACE1 mRNA by masking the binding site for miR-485-5p. Indeed, miR-485-5p and BACE1 -antisense compete for binding within the same region in the open reading frame of the BACE1 mRNA. We observed opposing effects of BACE1 -antisense and miR-485-5p on BACE1 protein in vitro and showed that Locked Nucleic Acid-antimiR mediated knockdown of miR-485-5p as well as BACE1 -antisense over-expression can prevent the miRNA-induced BACE1 suppression. We found that the expression of BACE1 -antisense as well as miR-485-5p are dysregulated in RNA samples from Alzheimer's disease subjects compared to control individuals. Conclusions: Our data demonstrate an interface between two distinct groups of regulatory RNAs in the computation of BACE1 gene expression. Moreover, bioinformatics analyses revealed a theoretical basis for many other potential interactions between natural antisense transcripts and miRNAs at the binding sites of the latter.
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BACE1-AS stabilizes BACE1 through competitive binding of miR-485-5p which would otherwise repress BACE1 mRNA translation.
“BACE1‐AS is reported to stabilize BACE1 through competitive binding of miR‐485‐5p which would otherwise repress BACE1 mRNA translation.”
From BACE1: More than just a β‐secretase (2022) · cites this paper as [56]
miR-485-5p is significantly downregulated in the parietal lobe, cerebellum, entorhinal cortex and hippocampus.
“Faghihi et al. [64] found that miR-485-5p was significantly downregulated in the parietal lobe, cerebellum, entorhinal cortex and hippocampus”
From MicroRNAs in Extracellular Vesicles of Alzheimer’s Disease (2023) · cites this paper as [64]
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Control of Peripheral Nerve Myelination by the ß-Secretase BACE1
Willem, M., Garratt, A. N., Novak, B., Citron, M., Kaufmann, S., Rittger, A., DeStrooper, B., Saftig, P., Birchmeier, C., & Haass, C. (2006) · Science · doi:10.1126/science.1132341 · Cited by 703
McConlogue, L., Buttini, M., Anderson, J. P., Brigham, E. F., Chen, K. S., Freedman, S. B., Games, D., Johnson-Wood, K., Lee, M., Zeller, M., et al. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m611687200 · Cited by 300 · cited 1×
“It should be noted that Aβ142 accumulation in the Alzheimer's disease brain is a long-lasting and chronic process and that even small changes in BACE1 activity may lead to a significant increase in amyloid deposition over time [50,51].”
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Metadata
- Authors
- Faghihi, M. A., Zhang, M., Huang, J., Modarresi, F., Van der Brug, M. P., Nalls, M. A., Cookson, M. R., St-Laurent, G., & Wahlestedt, C.
- Venue
- Genome Biology
- Published
- 2010-05-27
- Volume
- 11
- Issue
- 5
- ISSN
- 1474-760X
- PMC
- PMC2898074
- Cited by
- 473
- References
- 3
- Language
- en
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