Evidence map›Paper›PMID 29529991›Full record

ArticleBMC bioinformatics2018

Inferring RNA sequence preferences for poorly studied RNA-binding proteins based on co-evolution.

Shu Yang, Junwen Wang, Raymond T Ng

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In one paragraph

Article in BMC bioinformatics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

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7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Representation learning applications in biological sequence analysis.Computational and structural biotechnology journal · 2021
    Review
  5. Article
  6. Article
  7. Review
4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Shu YangDepartment of Computer Science, University of British Columbia, Vancouver, Canada. syang11@cs.ubc.ca.ORCID 0000-0002-8507-7191
Junwen WangDepartment of Health Sciences Research, Mayo Clinic Arizona, Scottsdale, USA.
Raymond T NgDepartment of Computer Science, University of British Columbia, Vancouver, Canada.

Funding

Genome Canada lsarpNatural Sciences and Engineering Research Council of Canada cnfn
6 · The paper itself

Abstract

backgroundCharacterizing the binding preference of RNA-binding proteins (RBP) is essential for us to understand the interaction between an RBP and its RNA targets, and to decipher the mechanism of post-transcriptional regulation. Experimental methods have been used to generate protein-RNA binding data for a number of RBPs in vivo and in vitro. Utilizing the binding data, a couple of computational methods have been developed to detect the RNA sequence or structure preferences of the RBPs. However, the majority of RBPs have not yet been experimentally characterized and lack RNA binding data. For these poorly studied RBPs, the identification of their binding preferences cannot be performed by most existing computational methods because the experimental binding data are prerequisite to these methods.

resultsHere we propose a new method based on co-evolution to predict the sequence preferences for the poorly studied RBPs, waiving the requirement of their binding data. First, we demonstrate the co-evolutionary relationship between RBPs and their RNA partners. We then present a K-nearest neighbors (KNN) based algorithm to infer the sequence preference of an RBP using only the preference information from its homologous RBPs. By benchmarking against several in vitro and in vivo datasets, our proposed method outperforms the existing alternative which uses the closest neighbor's preference on all the datasets. Moreover, it shows comparable performance with two state-of-the-art methods that require the presence of the experimental binding data. Finally, we demonstrate the usage of this method to infer sequence preferences for novel proteins which have no binding preference information available.

conclusionFor a poorly studied RBP, the current methods used to determine its binding preference need experimental data, which is expensive and time consuming. Therefore, determining RBP's preference is not practical in many situations. This study provides an economic solution to infer the sequence preference of such protein based on the co-evolution. The source codes and related datasets are available at https://github.com/syang11/KNN .

Indexed as

AlgorithmsEvolution, MolecularBinding SitesRNARNA-Binding ProteinsRNARNA-Binding ProteinsCo-evolutionK-nearest neighborsMachine learningRBP binding preference

Identifiers

PMID29529991
PMCPMC5848454

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.