Abstract
Circular RNAs (circRNAs) constitute an emerging class of widespread, abundant, and evolutionarily conserved noncoding RNA. They play important and diverse roles in cell development, growth, and tumorigenesis, but functions of the majority of circRNAs remain enigmatic. In order to investigate circRNA function it is necessary to manipulate its expression. While various standard approaches exist for circRNA knockdown, here we present cloning vectors for simplifying the laborious process of cloning circRNAs to achieve high-efficiency overexpression in mammalian cell lines.
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References
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Acknowledgments
Research reported in this publication was supported by the National Health and Medical Research Council (NHMRC) project grant funding to S.J.C. (GNT1089167) and G.J.G. (GNT1089167, GNT1068773, GNT1126711). Fellowship support was provided by the Australian Research Council Future Fellowship to S.J.C. (FT160100318) and NHMRC Research Fellowship to G.J.G. (GNT1118170).
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Liu, D., Conn, V., Goodall, G.J., Conn, S.J. (2018). A Highly Efficient Strategy for Overexpressing circRNAs. In: Dieterich, C., Papantonis, A. (eds) Circular RNAs. Methods in Molecular Biology, vol 1724. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-7562-4_8
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DOI: https://doi.org/10.1007/978-1-4939-7562-4_8
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