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Improved linking of motifs to their TFs using domain information
- Source :
- Bioinformatics
- Publication Year :
- 2019
- Publisher :
- Oxford University Press (OUP), 2019.
-
Abstract
- Motivation A central aim of molecular biology is to identify mechanisms of transcriptional regulation. Transcription factors (TFs), which are DNA-binding proteins, are highly involved in these processes, thus a crucial information is to know where TFs interact with DNA, and to be aware of the TFs’ DNA-binding motifs. For that reason, computational tools exist that link DNA-binding motifs to TFs either without sequence information or based on TF-associated sequences, e.g. identified via a ChIP-seq experiment. Method In this paper we present MASSIF, a novel method to improve the performance of existing tools that link motifs to TFs relying on TF-associated sequences. MASSIF is based on the idea that a DNA-binding motif, which is correctly linked to a TF, should be assigned to a DNA-binding domain (DBD) similar to that of the mapped TF. Because DNA-binding motifs are in general not linked to DBDs, it is not possible to compare the DBD of a TF and the motif directly. Instead we created a DBD collection, which consist of TFs with a known DBD and an associated motif. This collection enables us to evaluate how likely it is that a linked motif and a TF of interest are associated to the same DBD. We named this similarity measure domain score, and represent it as a p-value. We developed two different ways to improve the performance of existing tools that link motifs to TFs based on TF-associated sequences: (1) using meta analysis to combine p-values from one or several of these tools with the p-value of the domain score and (2) filter unlikely motifs based on the domain score. Results We demonstrate the functionality of MASSIF on several human ChIP-seq data sets, using either motifs from the HOCOMOCO database or de novo identified ones as input motifs. In addition, we show that both variants of our method improve the performance of tools that link motifs to TFs based on TF-associated sequences significantly independent of the considered DBD type. Availability MASSIF is freely available online at https://github.com/SchulzLab/MASSIF Supplementary information Supplementary data are available at Bioinformatics online.
- Subjects :
- Statistics and Probability
Chromatin Immunoprecipitation
Sequence analysis
Computer science
Nucleotide Motif
Review
Computational biology
Similarity measure
Biochemistry
DNA-binding protein
03 medical and health sciences
chemistry.chemical_compound
Transcriptional regulation
Nucleotide Motifs
Molecular Biology
Transcription factor
030304 developmental biology
0303 health sciences
Binding Sites
030302 biochemistry & molecular biology
Computational Biology
Sequence Analysis, DNA
Computer Science Applications
DNA-Binding Proteins
Computational Mathematics
Computational Theory and Mathematics
chemistry
Motif (music)
Sequence Analysis
Chromatin immunoprecipitation
DNA
Protein Binding
Transcription Factors
Subjects
Details
- ISSN :
- 14602059 and 13674803
- Database :
- OpenAIRE
- Journal :
- Bioinformatics
- Accession number :
- edsair.doi.dedup.....4f8150e7bea0de9d67acebbcc77facdc
- Full Text :
- https://doi.org/10.1093/bioinformatics/btz855