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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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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. |
format | Online Article Text |
id | pubmed-6364045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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