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Genome-wide polycomb target gene prediction in Drosophila melanogaster
As key epigenetic regulators, polycomb group (PcG) proteins are responsible for the control of cell proliferation and differentiation as well as stem cell pluripotency and self-renewal. Aberrant epigenetic modification by PcG is strongly correlated with the severity and invasiveness of many types of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401425/ https://www.ncbi.nlm.nih.gov/pubmed/22416065 http://dx.doi.org/10.1093/nar/gks209 |
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author | Zeng, Jia Kirk, Brian D. Gou, Yufeng Wang, Qinghua Ma, Jianpeng |
author_facet | Zeng, Jia Kirk, Brian D. Gou, Yufeng Wang, Qinghua Ma, Jianpeng |
author_sort | Zeng, Jia |
collection | PubMed |
description | As key epigenetic regulators, polycomb group (PcG) proteins are responsible for the control of cell proliferation and differentiation as well as stem cell pluripotency and self-renewal. Aberrant epigenetic modification by PcG is strongly correlated with the severity and invasiveness of many types of cancers. Unfortunately, the molecular mechanism of PcG-mediated epigenetic regulation remained elusive, partly due to the extremely limited pool of experimentally confirmed PcG target genes. In order to facilitate experimental identification of PcG target genes, here we propose a novel computational method, EpiPredictor, that achieved significantly higher matching ratios with several recent chromatin immunoprecipitation studies than jPREdictor, an existing computational method. We further validated a subset of genes that were uniquely predicted by EpiPredictor by cross-referencing existing literature and by experimental means. Our data suggest that multiple transcription factor networking at the cis-regulatory elements is critical for PcG recruitment, while high GC content and high conservation level are also important features of PcG target genes. EpiPredictor should substantially expedite experimental discovery of PcG target genes by providing an effective initial screening tool. From a computational standpoint, our strategy of modelling transcription factor interaction with a non-linear kernel is original, effective and transferable to many other applications. |
format | Online Article Text |
id | pubmed-3401425 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-34014252012-07-23 Genome-wide polycomb target gene prediction in Drosophila melanogaster Zeng, Jia Kirk, Brian D. Gou, Yufeng Wang, Qinghua Ma, Jianpeng Nucleic Acids Res Computational Biology As key epigenetic regulators, polycomb group (PcG) proteins are responsible for the control of cell proliferation and differentiation as well as stem cell pluripotency and self-renewal. Aberrant epigenetic modification by PcG is strongly correlated with the severity and invasiveness of many types of cancers. Unfortunately, the molecular mechanism of PcG-mediated epigenetic regulation remained elusive, partly due to the extremely limited pool of experimentally confirmed PcG target genes. In order to facilitate experimental identification of PcG target genes, here we propose a novel computational method, EpiPredictor, that achieved significantly higher matching ratios with several recent chromatin immunoprecipitation studies than jPREdictor, an existing computational method. We further validated a subset of genes that were uniquely predicted by EpiPredictor by cross-referencing existing literature and by experimental means. Our data suggest that multiple transcription factor networking at the cis-regulatory elements is critical for PcG recruitment, while high GC content and high conservation level are also important features of PcG target genes. EpiPredictor should substantially expedite experimental discovery of PcG target genes by providing an effective initial screening tool. From a computational standpoint, our strategy of modelling transcription factor interaction with a non-linear kernel is original, effective and transferable to many other applications. Oxford University Press 2012-07 2012-03-13 /pmc/articles/PMC3401425/ /pubmed/22416065 http://dx.doi.org/10.1093/nar/gks209 Text en © The Author(s) 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Computational Biology Zeng, Jia Kirk, Brian D. Gou, Yufeng Wang, Qinghua Ma, Jianpeng Genome-wide polycomb target gene prediction in Drosophila melanogaster |
title | Genome-wide polycomb target gene prediction in Drosophila melanogaster |
title_full | Genome-wide polycomb target gene prediction in Drosophila melanogaster |
title_fullStr | Genome-wide polycomb target gene prediction in Drosophila melanogaster |
title_full_unstemmed | Genome-wide polycomb target gene prediction in Drosophila melanogaster |
title_short | Genome-wide polycomb target gene prediction in Drosophila melanogaster |
title_sort | genome-wide polycomb target gene prediction in drosophila melanogaster |
topic | Computational Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401425/ https://www.ncbi.nlm.nih.gov/pubmed/22416065 http://dx.doi.org/10.1093/nar/gks209 |
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