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Enhanced Tailored MicroRNA Sponge Activity of RNA Pol II-Transcribed TuD Hairpins Relative to Ectopically Expressed ciRS7-Derived circRNAs

As key regulators of gene expression, microRNAs (miRNAs) have emerged as targets in basic experimentation and therapy. Administration of DNA-encoded RNA molecules, targeting miRNAs through base pairing, is one viable strategy for inhibiting specific miRNAs. A naturally occurring circular RNA (circRN...

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Autores principales: Hollensen, Anne Kruse, Andersen, Sofie, Hjorth, Karina, Bak, Rasmus O., Hansen, Thomas B., Kjems, Jørgen, Aagaard, Lars, Damgaard, Christian Kroun, Mikkelsen, Jacob Giehm
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6198105/
https://www.ncbi.nlm.nih.gov/pubmed/30347350
http://dx.doi.org/10.1016/j.omtn.2018.09.009
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author Hollensen, Anne Kruse
Andersen, Sofie
Hjorth, Karina
Bak, Rasmus O.
Hansen, Thomas B.
Kjems, Jørgen
Aagaard, Lars
Damgaard, Christian Kroun
Mikkelsen, Jacob Giehm
author_facet Hollensen, Anne Kruse
Andersen, Sofie
Hjorth, Karina
Bak, Rasmus O.
Hansen, Thomas B.
Kjems, Jørgen
Aagaard, Lars
Damgaard, Christian Kroun
Mikkelsen, Jacob Giehm
author_sort Hollensen, Anne Kruse
collection PubMed
description As key regulators of gene expression, microRNAs (miRNAs) have emerged as targets in basic experimentation and therapy. Administration of DNA-encoded RNA molecules, targeting miRNAs through base pairing, is one viable strategy for inhibiting specific miRNAs. A naturally occurring circular RNA (circRNA), ciRS-7, serving as a miRNA-7 (miR-7) sponge was recently identified. This has sparked tremendous interest in adapting circRNAs for suppressing miRNA function. In parallel, we and others have demonstrated efficacy of expressed anti-miRNA Tough Decoy (TuD) hairpins. To compare properties of such inhibitors, we express ciRS-7 and TuD-containing miRNA suppressor transcripts from identical vector formats adapted from RNA polymerase II-directed expression plasmids previously used for production of ciRS-7. In general, markedly higher levels of miR-7 suppression with TuD transcripts relative to ciRS-7 are observed, leading to superior miRNA sponge effects using expressed TuD hairpins. Notably however, we find that individual ciRS-7 transcripts are more potent inhibitors of miR-7 activity than individual TuD7-containing transcripts, although each miR-7 seed match target site in ciRS-7 is, on average, less potent than the perfectly matched target sites in the TuD motif. All together, our studies call for improved means of designing and producing circRNAs for customized miRNA targeting to match TuD hairpins for tailored miRNA suppression.
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spelling pubmed-61981052018-10-24 Enhanced Tailored MicroRNA Sponge Activity of RNA Pol II-Transcribed TuD Hairpins Relative to Ectopically Expressed ciRS7-Derived circRNAs Hollensen, Anne Kruse Andersen, Sofie Hjorth, Karina Bak, Rasmus O. Hansen, Thomas B. Kjems, Jørgen Aagaard, Lars Damgaard, Christian Kroun Mikkelsen, Jacob Giehm Mol Ther Nucleic Acids Article As key regulators of gene expression, microRNAs (miRNAs) have emerged as targets in basic experimentation and therapy. Administration of DNA-encoded RNA molecules, targeting miRNAs through base pairing, is one viable strategy for inhibiting specific miRNAs. A naturally occurring circular RNA (circRNA), ciRS-7, serving as a miRNA-7 (miR-7) sponge was recently identified. This has sparked tremendous interest in adapting circRNAs for suppressing miRNA function. In parallel, we and others have demonstrated efficacy of expressed anti-miRNA Tough Decoy (TuD) hairpins. To compare properties of such inhibitors, we express ciRS-7 and TuD-containing miRNA suppressor transcripts from identical vector formats adapted from RNA polymerase II-directed expression plasmids previously used for production of ciRS-7. In general, markedly higher levels of miR-7 suppression with TuD transcripts relative to ciRS-7 are observed, leading to superior miRNA sponge effects using expressed TuD hairpins. Notably however, we find that individual ciRS-7 transcripts are more potent inhibitors of miR-7 activity than individual TuD7-containing transcripts, although each miR-7 seed match target site in ciRS-7 is, on average, less potent than the perfectly matched target sites in the TuD motif. All together, our studies call for improved means of designing and producing circRNAs for customized miRNA targeting to match TuD hairpins for tailored miRNA suppression. American Society of Gene & Cell Therapy 2018-09-21 /pmc/articles/PMC6198105/ /pubmed/30347350 http://dx.doi.org/10.1016/j.omtn.2018.09.009 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hollensen, Anne Kruse
Andersen, Sofie
Hjorth, Karina
Bak, Rasmus O.
Hansen, Thomas B.
Kjems, Jørgen
Aagaard, Lars
Damgaard, Christian Kroun
Mikkelsen, Jacob Giehm
Enhanced Tailored MicroRNA Sponge Activity of RNA Pol II-Transcribed TuD Hairpins Relative to Ectopically Expressed ciRS7-Derived circRNAs
title Enhanced Tailored MicroRNA Sponge Activity of RNA Pol II-Transcribed TuD Hairpins Relative to Ectopically Expressed ciRS7-Derived circRNAs
title_full Enhanced Tailored MicroRNA Sponge Activity of RNA Pol II-Transcribed TuD Hairpins Relative to Ectopically Expressed ciRS7-Derived circRNAs
title_fullStr Enhanced Tailored MicroRNA Sponge Activity of RNA Pol II-Transcribed TuD Hairpins Relative to Ectopically Expressed ciRS7-Derived circRNAs
title_full_unstemmed Enhanced Tailored MicroRNA Sponge Activity of RNA Pol II-Transcribed TuD Hairpins Relative to Ectopically Expressed ciRS7-Derived circRNAs
title_short Enhanced Tailored MicroRNA Sponge Activity of RNA Pol II-Transcribed TuD Hairpins Relative to Ectopically Expressed ciRS7-Derived circRNAs
title_sort enhanced tailored microrna sponge activity of rna pol ii-transcribed tud hairpins relative to ectopically expressed cirs7-derived circrnas
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6198105/
https://www.ncbi.nlm.nih.gov/pubmed/30347350
http://dx.doi.org/10.1016/j.omtn.2018.09.009
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