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Design and application of circular RNAs with protein-sponge function

Circular RNAs (circRNAs) are a class of noncoding RNAs, generated from pre-mRNAs by circular splicing of exons and functionally largely uncharacterized. Here we report on the design, expression, and characterization of artificial circRNAs that act as protein sponges, specifically binding and functio...

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Autores principales: Schreiner, Silke, Didio, Anna, Hung, Lee-Hsueh, Bindereif, Albrecht
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708053/
https://www.ncbi.nlm.nih.gov/pubmed/33231682
http://dx.doi.org/10.1093/nar/gkaa1085
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author Schreiner, Silke
Didio, Anna
Hung, Lee-Hsueh
Bindereif, Albrecht
author_facet Schreiner, Silke
Didio, Anna
Hung, Lee-Hsueh
Bindereif, Albrecht
author_sort Schreiner, Silke
collection PubMed
description Circular RNAs (circRNAs) are a class of noncoding RNAs, generated from pre-mRNAs by circular splicing of exons and functionally largely uncharacterized. Here we report on the design, expression, and characterization of artificial circRNAs that act as protein sponges, specifically binding and functionally inactivating hnRNP (heterogeneous nuclear ribonucleoprotein) L. HnRNP L regulates alternative splicing, depending on short CA-rich RNA elements. We demonstrate that designer hnRNP L-sponge circRNAs with CA-repeat or CA-rich sequence clusters can efficiently and specifically modulate splicing-regulatory networks in mammalian cells, including alternative splicing patterns and the cellular distribution of a splicing factor. This new strategy can in principle be applied to any RNA-binding protein, opening up new therapeutic strategies in molecular medicine.
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spelling pubmed-77080532020-12-07 Design and application of circular RNAs with protein-sponge function Schreiner, Silke Didio, Anna Hung, Lee-Hsueh Bindereif, Albrecht Nucleic Acids Res RNA and RNA-protein complexes Circular RNAs (circRNAs) are a class of noncoding RNAs, generated from pre-mRNAs by circular splicing of exons and functionally largely uncharacterized. Here we report on the design, expression, and characterization of artificial circRNAs that act as protein sponges, specifically binding and functionally inactivating hnRNP (heterogeneous nuclear ribonucleoprotein) L. HnRNP L regulates alternative splicing, depending on short CA-rich RNA elements. We demonstrate that designer hnRNP L-sponge circRNAs with CA-repeat or CA-rich sequence clusters can efficiently and specifically modulate splicing-regulatory networks in mammalian cells, including alternative splicing patterns and the cellular distribution of a splicing factor. This new strategy can in principle be applied to any RNA-binding protein, opening up new therapeutic strategies in molecular medicine. Oxford University Press 2020-11-24 /pmc/articles/PMC7708053/ /pubmed/33231682 http://dx.doi.org/10.1093/nar/gkaa1085 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle RNA and RNA-protein complexes
Schreiner, Silke
Didio, Anna
Hung, Lee-Hsueh
Bindereif, Albrecht
Design and application of circular RNAs with protein-sponge function
title Design and application of circular RNAs with protein-sponge function
title_full Design and application of circular RNAs with protein-sponge function
title_fullStr Design and application of circular RNAs with protein-sponge function
title_full_unstemmed Design and application of circular RNAs with protein-sponge function
title_short Design and application of circular RNAs with protein-sponge function
title_sort design and application of circular rnas with protein-sponge function
topic RNA and RNA-protein complexes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708053/
https://www.ncbi.nlm.nih.gov/pubmed/33231682
http://dx.doi.org/10.1093/nar/gkaa1085
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