RT Journal Article
SR Electronic
T1 SSMART: Sequence-structure motif identification for RNA-binding proteins
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 287953
DO 10.1101/287953
A1 Munteanu, Alina
A1 Mukherjee, Neelanjan
A1 Ohler, Uwe
YR 2018
UL http://biorxiv.org/content/early/2018/03/23/287953.abstract
AB Motivation RNA-binding proteins (RBPs) regulate every aspect of RNA metabolism and function. There are hundreds of RBPs encoded in the eukaryotic genomes, and each recognize its RNA targets through a specific mixture of RNA sequence and structure properties. For most RBPs, however, only a primary sequence motif has been determined, while the structure of the binding sites is uncharacterized.Results We developed SSMART, an RNA motif finder that simultaneously models the primary sequence and the structural properties of the RNA targets sites. The sequence-structure motifs are represented as consensus strings over a degenerate alphabet, extending the IUPAC codes for nucleotides to account for secondary structure preferences. Evaluation on synthetic data showed that SSMART is able to recover both sequence and structure motifs implanted into 3‘UTR-like sequences, for various degrees of structured/unstructured binding sites. In addition, we successfully used SSMART on high-throughput in vivo and in vitro data, showing that we not only recover the known sequence motif, but also gain insight into the structural preferences of the RBP.Availability SSMART is freely available at https://ohlerlab.mdc-berlin.de/software/SSMART_137/Contact uwe.ohler{at}mdc-berlin.de