Recognition of interferon-inducible sites, promoters, and enhancers

<p>Abstract</p> <p>Background</p> <p>Computational analysis of gene regulatory regions is important for prediction of functions of many uncharacterized genes. With this in mind, search of the target genes for interferon (IFN) induction appears of interest. IFNs are mult...

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Main Authors: Kondrakhin Yury V, Ananko Elena A, Merkulova Tatiana I, Kolchanov Nikolay A
Format: Article
Language:English
Published: BMC 2007-02-01
Series:BMC Bioinformatics
Online Access:http://www.biomedcentral.com/1471-2105/8/56
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spelling doaj-2301dd9edba94c10bbd413556bd1b5912020-11-24T21:19:07ZengBMCBMC Bioinformatics1471-21052007-02-01815610.1186/1471-2105-8-56Recognition of interferon-inducible sites, promoters, and enhancersKondrakhin Yury VAnanko Elena AMerkulova Tatiana IKolchanov Nikolay A<p>Abstract</p> <p>Background</p> <p>Computational analysis of gene regulatory regions is important for prediction of functions of many uncharacterized genes. With this in mind, search of the target genes for interferon (IFN) induction appears of interest. IFNs are multi-functional cytokines. Their effects are immunomodulatory, antiviral, antibacterial, and antitumor. The interaction of the IFNs with their cell surface receptors produces an activation of several transcription factors. Four regulatory factors, ISGF3, STAT1, IRF1, and NF-κB, are essential for the function of the IFN system. The aim of this work is the development of computational approaches for the recognition of DNA binding sites for these factors and computer programs for the prediction of the IFN-inducible regions.</p> <p>Results</p> <p>We developed computational approaches to the recognition of the binding sites for ISGF3, STAT1, IRF1, and NF-κB. Analysis of the distribution of these binding sites demonstrated that the regions -500 upstream of the transcription start site in IFN-inducible genes are enriched in putative binding sites for these transcription factors. Based on selected combinations of the sites whose frequencies were significantly higher than in the other functional gene groups, we developed methods for the prediction of the IFN-inducible promoters and enhancers. We analyzed 1004 sequences of the IFN-inducible genes compiled using microarray data analyses and also about 10,000 human gene sequences from the EPD and RefSeq databases; 74 of 1,664 human genes annotated in EPD were significantly IFN-inducible.</p> <p>Conclusion</p> <p>Analyses of several control datasets demonstrated that the developed methods have a high accuracy of prediction of the IFN-inducible genes. Application of these methods to several datasets suggested that the number of the IFN-inducible genes is approximately 1500–2000 in the human genome.</p> http://www.biomedcentral.com/1471-2105/8/56
collection DOAJ
language English
format Article
sources DOAJ
author Kondrakhin Yury V
Ananko Elena A
Merkulova Tatiana I
Kolchanov Nikolay A
spellingShingle Kondrakhin Yury V
Ananko Elena A
Merkulova Tatiana I
Kolchanov Nikolay A
Recognition of interferon-inducible sites, promoters, and enhancers
BMC Bioinformatics
author_facet Kondrakhin Yury V
Ananko Elena A
Merkulova Tatiana I
Kolchanov Nikolay A
author_sort Kondrakhin Yury V
title Recognition of interferon-inducible sites, promoters, and enhancers
title_short Recognition of interferon-inducible sites, promoters, and enhancers
title_full Recognition of interferon-inducible sites, promoters, and enhancers
title_fullStr Recognition of interferon-inducible sites, promoters, and enhancers
title_full_unstemmed Recognition of interferon-inducible sites, promoters, and enhancers
title_sort recognition of interferon-inducible sites, promoters, and enhancers
publisher BMC
series BMC Bioinformatics
issn 1471-2105
publishDate 2007-02-01
description <p>Abstract</p> <p>Background</p> <p>Computational analysis of gene regulatory regions is important for prediction of functions of many uncharacterized genes. With this in mind, search of the target genes for interferon (IFN) induction appears of interest. IFNs are multi-functional cytokines. Their effects are immunomodulatory, antiviral, antibacterial, and antitumor. The interaction of the IFNs with their cell surface receptors produces an activation of several transcription factors. Four regulatory factors, ISGF3, STAT1, IRF1, and NF-κB, are essential for the function of the IFN system. The aim of this work is the development of computational approaches for the recognition of DNA binding sites for these factors and computer programs for the prediction of the IFN-inducible regions.</p> <p>Results</p> <p>We developed computational approaches to the recognition of the binding sites for ISGF3, STAT1, IRF1, and NF-κB. Analysis of the distribution of these binding sites demonstrated that the regions -500 upstream of the transcription start site in IFN-inducible genes are enriched in putative binding sites for these transcription factors. Based on selected combinations of the sites whose frequencies were significantly higher than in the other functional gene groups, we developed methods for the prediction of the IFN-inducible promoters and enhancers. We analyzed 1004 sequences of the IFN-inducible genes compiled using microarray data analyses and also about 10,000 human gene sequences from the EPD and RefSeq databases; 74 of 1,664 human genes annotated in EPD were significantly IFN-inducible.</p> <p>Conclusion</p> <p>Analyses of several control datasets demonstrated that the developed methods have a high accuracy of prediction of the IFN-inducible genes. Application of these methods to several datasets suggested that the number of the IFN-inducible genes is approximately 1500–2000 in the human genome.</p>
url http://www.biomedcentral.com/1471-2105/8/56
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