RT Journal Article
SR Electronic
T1 The discovery potential of RNA processing profiles
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 049809
DO 10.1101/049809
A1 Amadís Pagès
A1 Ivan Dotu
A1 Joan Pallarès-Albanell
A1 Eulàlia Martí
A1 Roderic Guigó
A1 Eduardo Eyras
YR 2017
UL http://biorxiv.org/content/early/2017/07/31/049809.abstract
AB Small non-coding RNAs are highly abundant molecules that regulate essential cellular processes and are classified according to sequence and structure. Here we argue that read profiles from size-selected RNA sequencing capture the post-transcriptional processing specific to each RNA family, thereby providing functional information independently of sequence and structure. We developed SeRPeNT, the first unsupervised computational method that exploits reproducibility across replicates and uses dynamic time-warping and density-based clustering algorithms to identify, characterize and compare small non-coding RNAs (sncRNAs) by harnessing the power of read profiles. We applied SeRPeNT to: a) generate an extended human annotation with 671 new sncRNAs from known classes and 131 from new potential classes, b) show pervasive differential processing between cell compartments and c) predict new molecules with miRNA-like behaviour from snoRNA, tRNA and long non-coding RNA precursors, potentially dependent on the miRNA biogenesis pathway. Furthermore, we validated experimentally four predicted novel non-coding RNAs: a miRNA, a snoRNA-derived miRNA, a processed tRNA and a new uncharacterized sncRNA. SeRPeNT facilitates fast and accurate discovery and characterization of small non-coding RNAs at unprecedented scale. SeRPeNT code is available under the MIT license at https://github.com/comprna/SeRPeNT.