Cataloging mammalian circular RNAs
Thousands of mammalian circRNAs arise by back-splicing and can be quantified across ENCODE cell types.
Source
Expanded identification and characterization of mammalian circular RNAs
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
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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 [].
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.
More on Gene expression