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APRICOT: an integrated computational pipeline for the sequence-based identification and characterization of RNA-binding proteins
RNA-binding proteins (RBPs) have been established as core components of several post-transcriptional gene regulation mechanisms. Experimental techniques such as cross-linking and co-immunoprecipitation have enabled the identification of RBPs, RNA-binding domains (RBDs) and their regulatory roles in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499795/ https://www.ncbi.nlm.nih.gov/pubmed/28334975 http://dx.doi.org/10.1093/nar/gkx137 |
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author | Sharan, Malvika Förstner, Konrad U. Eulalio, Ana Vogel, Jörg |
author_facet | Sharan, Malvika Förstner, Konrad U. Eulalio, Ana Vogel, Jörg |
author_sort | Sharan, Malvika |
collection | PubMed |
description | RNA-binding proteins (RBPs) have been established as core components of several post-transcriptional gene regulation mechanisms. Experimental techniques such as cross-linking and co-immunoprecipitation have enabled the identification of RBPs, RNA-binding domains (RBDs) and their regulatory roles in the eukaryotic species such as human and yeast in large-scale. In contrast, our knowledge of the number and potential diversity of RBPs in bacteria is poorer due to the technical challenges associated with the existing global screening approaches. We introduce APRICOT, a computational pipeline for the sequence-based identification and characterization of proteins using RBDs known from experimental studies. The pipeline identifies functional motifs in protein sequences using position-specific scoring matrices and Hidden Markov Models of the functional domains and statistically scores them based on a series of sequence-based features. Subsequently, APRICOT identifies putative RBPs and characterizes them by several biological properties. Here we demonstrate the application and adaptability of the pipeline on large-scale protein sets, including the bacterial proteome of Escherichia coli. APRICOT showed better performance on various datasets compared to other existing tools for the sequence-based prediction of RBPs by achieving an average sensitivity and specificity of 0.90 and 0.91 respectively. The command-line tool and its documentation are available at https://pypi.python.org/pypi/bio-apricot. |
format | Online Article Text |
id | pubmed-5499795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54997952017-07-12 APRICOT: an integrated computational pipeline for the sequence-based identification and characterization of RNA-binding proteins Sharan, Malvika Förstner, Konrad U. Eulalio, Ana Vogel, Jörg Nucleic Acids Res Methods Online RNA-binding proteins (RBPs) have been established as core components of several post-transcriptional gene regulation mechanisms. Experimental techniques such as cross-linking and co-immunoprecipitation have enabled the identification of RBPs, RNA-binding domains (RBDs) and their regulatory roles in the eukaryotic species such as human and yeast in large-scale. In contrast, our knowledge of the number and potential diversity of RBPs in bacteria is poorer due to the technical challenges associated with the existing global screening approaches. We introduce APRICOT, a computational pipeline for the sequence-based identification and characterization of proteins using RBDs known from experimental studies. The pipeline identifies functional motifs in protein sequences using position-specific scoring matrices and Hidden Markov Models of the functional domains and statistically scores them based on a series of sequence-based features. Subsequently, APRICOT identifies putative RBPs and characterizes them by several biological properties. Here we demonstrate the application and adaptability of the pipeline on large-scale protein sets, including the bacterial proteome of Escherichia coli. APRICOT showed better performance on various datasets compared to other existing tools for the sequence-based prediction of RBPs by achieving an average sensitivity and specificity of 0.90 and 0.91 respectively. The command-line tool and its documentation are available at https://pypi.python.org/pypi/bio-apricot. Oxford University Press 2017-06-20 2017-03-02 /pmc/articles/PMC5499795/ /pubmed/28334975 http://dx.doi.org/10.1093/nar/gkx137 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methods Online Sharan, Malvika Förstner, Konrad U. Eulalio, Ana Vogel, Jörg APRICOT: an integrated computational pipeline for the sequence-based identification and characterization of RNA-binding proteins |
title | APRICOT: an integrated computational pipeline for the sequence-based identification and characterization of RNA-binding proteins |
title_full | APRICOT: an integrated computational pipeline for the sequence-based identification and characterization of RNA-binding proteins |
title_fullStr | APRICOT: an integrated computational pipeline for the sequence-based identification and characterization of RNA-binding proteins |
title_full_unstemmed | APRICOT: an integrated computational pipeline for the sequence-based identification and characterization of RNA-binding proteins |
title_short | APRICOT: an integrated computational pipeline for the sequence-based identification and characterization of RNA-binding proteins |
title_sort | apricot: an integrated computational pipeline for the sequence-based identification and characterization of rna-binding proteins |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499795/ https://www.ncbi.nlm.nih.gov/pubmed/28334975 http://dx.doi.org/10.1093/nar/gkx137 |
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