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TELS: A Novel Computational Framework for Identifying Motif Signatures of Transcribed Enhancers

In mammalian cells, transcribed enhancers (TrEns) play important roles in the initiation of gene expression and maintenance of gene expression levels in a spatiotemporal manner. One of the most challenging questions is how the genomic characteristics of enhancers relate to enhancer activities. To da...

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Detalles Bibliográficos
Autores principales: Kleftogiannis, Dimitrios, Ashoor, Haitham, Bajic, Vladimir B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6364045/
https://www.ncbi.nlm.nih.gov/pubmed/30578915
http://dx.doi.org/10.1016/j.gpb.2018.05.003
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author Kleftogiannis, Dimitrios
Ashoor, Haitham
Bajic, Vladimir B.
author_facet Kleftogiannis, Dimitrios
Ashoor, Haitham
Bajic, Vladimir B.
author_sort Kleftogiannis, Dimitrios
collection PubMed
description In mammalian cells, transcribed enhancers (TrEns) play important roles in the initiation of gene expression and maintenance of gene expression levels in a spatiotemporal manner. One of the most challenging questions is how the genomic characteristics of enhancers relate to enhancer activities. To date, only a limited number of enhancer sequence characteristics have been investigated, leaving space for exploring the enhancers’ DNA code in a more systematic way. To address this problem, we developed a novel computational framework, Transcribed Enhancer Landscape Search (TELS), aimed at identifying predictive cell type/tissue-specific motif signatures of TrEns. As a case study, we used TELS to compile a comprehensive catalog of motif signatures for all known TrEns identified by the FANTOM5 consortium across 112 human primary cells and tissues. Our results confirm that combinations of different short motifs characterize in an optimized manner cell type/tissue-specific TrEns. Our study is the first to report combinations of motifs that maximize classification performance of TrEns exclusively transcribed in one cell type/tissue from TrEns exclusively transcribed in different cell types/tissues. Moreover, we also report 31 motif signatures predictive of enhancers’ broad activity. TELS codes and material are publicly available at http://www.cbrc.kaust.edu.sa/TELS.
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spelling pubmed-63640452019-02-15 TELS: A Novel Computational Framework for Identifying Motif Signatures of Transcribed Enhancers Kleftogiannis, Dimitrios Ashoor, Haitham Bajic, Vladimir B. Genomics Proteomics Bioinformatics Method In mammalian cells, transcribed enhancers (TrEns) play important roles in the initiation of gene expression and maintenance of gene expression levels in a spatiotemporal manner. One of the most challenging questions is how the genomic characteristics of enhancers relate to enhancer activities. To date, only a limited number of enhancer sequence characteristics have been investigated, leaving space for exploring the enhancers’ DNA code in a more systematic way. To address this problem, we developed a novel computational framework, Transcribed Enhancer Landscape Search (TELS), aimed at identifying predictive cell type/tissue-specific motif signatures of TrEns. As a case study, we used TELS to compile a comprehensive catalog of motif signatures for all known TrEns identified by the FANTOM5 consortium across 112 human primary cells and tissues. Our results confirm that combinations of different short motifs characterize in an optimized manner cell type/tissue-specific TrEns. Our study is the first to report combinations of motifs that maximize classification performance of TrEns exclusively transcribed in one cell type/tissue from TrEns exclusively transcribed in different cell types/tissues. Moreover, we also report 31 motif signatures predictive of enhancers’ broad activity. TELS codes and material are publicly available at http://www.cbrc.kaust.edu.sa/TELS. Elsevier 2018-10 2018-12-19 /pmc/articles/PMC6364045/ /pubmed/30578915 http://dx.doi.org/10.1016/j.gpb.2018.05.003 Text en © 2019 The Authors. Production and hosting by Elsevier B.V. on behalf of Beijing Institute of Genomics, Chinese Academy of Sciences and Genetics Society of China. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Method
Kleftogiannis, Dimitrios
Ashoor, Haitham
Bajic, Vladimir B.
TELS: A Novel Computational Framework for Identifying Motif Signatures of Transcribed Enhancers
title TELS: A Novel Computational Framework for Identifying Motif Signatures of Transcribed Enhancers
title_full TELS: A Novel Computational Framework for Identifying Motif Signatures of Transcribed Enhancers
title_fullStr TELS: A Novel Computational Framework for Identifying Motif Signatures of Transcribed Enhancers
title_full_unstemmed TELS: A Novel Computational Framework for Identifying Motif Signatures of Transcribed Enhancers
title_short TELS: A Novel Computational Framework for Identifying Motif Signatures of Transcribed Enhancers
title_sort tels: a novel computational framework for identifying motif signatures of transcribed enhancers
topic Method
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6364045/
https://www.ncbi.nlm.nih.gov/pubmed/30578915
http://dx.doi.org/10.1016/j.gpb.2018.05.003
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