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Cataloging mammalian circular RNAs

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Thousands of mammalian circRNAs arise by back-splicing and can be quantified across ENCODE cell types.

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Expanded identification and characterization of mammalian circular RNAs

Guo JU, Agarwal V, Guo H, et al. · Genome biology · 2014

doi.org/10.1186/s13059-014-0409-zRead the full paper ↗1,316 citationscc by

Study at a glance

Design
Computational / modelling — Computational detection of back-splice junctions in non-poly(A) RNA-seq
N
Multi-sample circRNA discovery pipeline — no single primary analytic N in stored summary
Population
Mammalian non-poly(A) RNA-seq libraries
Outcome
Expanded catalogue and splice features of circular RNAs

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Cataloging mammalian circular RNAs

These passages occur verbatim in the stored paper text. They support the points listed below; they do not verify every statement in the explanation.

Mammalian circular RNAs.

Background Many classes of non-protein-coding RNAs (ncRNAs) exist in cells [,], and members of each class play important roles in either regulating gene expression or other biological processes [–].

Back-splicing of pre-mRNA.

For example, microRNAs (miRNAs) pair to sites within messenger RNAs (mRNAs) to target the mRNAs for translational repression and/or mRNA destabilization [].
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What they did

Built a computational pipeline on non-poly(A) RNA-seq to detect back-splice junctions and circular fractions.

What they found

Most confident circRNAs use canonical GT-AG splice signals; circular fractions vary by locus and cell type.

The limits

What it doesn't show

Does not prove sponge function for most newly found circRNAs.

Key terms

circRNA
Covalently circular RNA isoform.
Back-splicing
Donor joins upstream acceptor.
miRNA sponge
RNA that titrates miRNAs.
ENCODE
Large functional genomics consortium.
Circular fraction
Share of circular vs linear isoform.
GT-AG
Canonical splice-site dinucleotides.

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Common questions

Biogenesis?

Back-splicing.

Data?

ENCODE RNA-seq.

Splice signals?

Mostly GT-AG.

Example sponge?

CDR1as.

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