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RPAD (RNase R treatment, polyadenylation, and poly(A)+ RNA depletion) method to isolate highly pure circular RNA.

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TLDR
RPAD enables the elucidation of circRNA biogenesis, sequence, and function by facilitating the isolation of highly pure circRNAs from total RNA pools.
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This article is published in Methods.The article was published on 2019-02-15 and is currently open access. It has received 47 citations till now. The article focuses on the topics: Circular RNA & RNA.

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Integration of bioinformatic predictions and experimental data to identify circRNA-miRNA associations

TL;DR: The potential to define miRNA “sponging” as a more general function of circRNAs is explored, the different approaches to predict miRNA response elements (MREs) in known or novel circRNA sequences are described and experiments based on Ago2-IP and experimentally validated miRNA:target duplexes are discussed.
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circSamd4 represses myogenic transcriptional activity of PUR proteins

TL;DR: RNA sequencing analysis of circRNAs differentially expressed during myogenesis revealed that circSamd4 expression increased robustly in mouse C2C12 myoblasts differentiating into myotubes, and the association of PUR proteins with circSamD4 enhances myogenesis by contributing to the derepression of MHC transcription.
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Noncoding RNAs in Cardiovascular Disease: Current Knowledge, Tools and Technologies for Investigation, and Future Directions: A Scientific Statement From the American Heart Association.

TL;DR: The use of network approaches and advanced computational tools to understand the interaction of different noncoding RNA species to mediate a particular phenotype may be required to fully comprehend the function of nonc coding RNAs in mediating disease phenotypes.
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Circular RNAs-The Road Less Traveled.

TL;DR: The possible mechanism of circular RNA biogenesis, its structure, properties, degradation, and the growing amount of evidence regarding the detection methods and its role in animal and plant systems are discussed.
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Computational approaches for circular RNA analysis.

TL;DR: An overview on different computational analysis tools and pipelines that became available throughout the last years of circRNAs research is provided and a set of valuable validation strategies, in silico as well as in vitro‐based approaches are provided.
References
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Journal ArticleDOI

Primer3—new capabilities and interfaces

TL;DR: Primer3’s current capabilities are described, including more accurate thermodynamic models in the primer design process, both to improve melting temperature prediction and to reduce the likelihood that primers will form hairpins or dimers.
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Circular RNAs are a large class of animal RNAs with regulatory potency

TL;DR: It is found that a human circRNA, antisense to the cerebellar degeneration-related protein 1 transcript (CDR1as), is densely bound by microRNA (miRNA) effector complexes and harbours 63 conserved binding sites for the ancient miRNA miR-7.
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Natural RNA circles function as efficient microRNA sponges

TL;DR: This study serves as the first functional analysis of a naturally expressed circular RNA, ciRS-7, which contains more than 70 selectively conserved miRNA target sites, and is highly and widely associated with Argonaute proteins in a miR-7-dependent manner.
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Circular RNAs are abundant, conserved, and associated with ALU repeats

TL;DR: High-throughput sequencing of libraries prepared from ribosome-depleted RNA with or without digestion with the RNA exonuclease showed that ecircRNAs are abundant, stable, conserved and nonrandom products of RNA splicing that could be involved in control of gene expression.
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