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Identification of Direct Target Genes Using Joint Sequence and Expression Likelihood with Application to DAF-16
A major challenge in the post-genome era is to reconstruct regulatory networks from the biological knowledge accumulated up to date. The development of tools for identifying direct target genes of transcription factors (TFs) is critical to this endeavor. Given a set of microarray experiments, a prob...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2266795/ https://www.ncbi.nlm.nih.gov/pubmed/18350157 http://dx.doi.org/10.1371/journal.pone.0001821 |
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author | Yu, Ron X. Liu, Jie True, Nick Wang, Wei |
author_facet | Yu, Ron X. Liu, Jie True, Nick Wang, Wei |
author_sort | Yu, Ron X. |
collection | PubMed |
description | A major challenge in the post-genome era is to reconstruct regulatory networks from the biological knowledge accumulated up to date. The development of tools for identifying direct target genes of transcription factors (TFs) is critical to this endeavor. Given a set of microarray experiments, a probabilistic model called TRANSMODIS has been developed which can infer the direct targets of a TF by integrating sequence motif, gene expression and ChIP-chip data. The performance of TRANSMODIS was first validated on a set of transcription factor perturbation experiments (TFPEs) involving Pho4p, a well studied TF in Saccharomyces cerevisiae. TRANSMODIS removed elements of arbitrariness in manual target gene selection process and produced results that concur with one's intuition. TRANSMODIS was further validated on a genome-wide scale by comparing it with two other methods in Saccharomyces cerevisiae. The usefulness of TRANSMODIS was then demonstrated by applying it to the identification of direct targets of DAF-16, a critical TF regulating ageing in Caenorhabditis elegans. We found that 189 genes were tightly regulated by DAF-16. In addition, DAF-16 has differential preference for motifs when acting as an activator or repressor, which awaits experimental verification. TRANSMODIS is computationally efficient and robust, making it a useful probabilistic framework for finding immediate targets. |
format | Text |
id | pubmed-2266795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-22667952008-03-19 Identification of Direct Target Genes Using Joint Sequence and Expression Likelihood with Application to DAF-16 Yu, Ron X. Liu, Jie True, Nick Wang, Wei PLoS One Research Article A major challenge in the post-genome era is to reconstruct regulatory networks from the biological knowledge accumulated up to date. The development of tools for identifying direct target genes of transcription factors (TFs) is critical to this endeavor. Given a set of microarray experiments, a probabilistic model called TRANSMODIS has been developed which can infer the direct targets of a TF by integrating sequence motif, gene expression and ChIP-chip data. The performance of TRANSMODIS was first validated on a set of transcription factor perturbation experiments (TFPEs) involving Pho4p, a well studied TF in Saccharomyces cerevisiae. TRANSMODIS removed elements of arbitrariness in manual target gene selection process and produced results that concur with one's intuition. TRANSMODIS was further validated on a genome-wide scale by comparing it with two other methods in Saccharomyces cerevisiae. The usefulness of TRANSMODIS was then demonstrated by applying it to the identification of direct targets of DAF-16, a critical TF regulating ageing in Caenorhabditis elegans. We found that 189 genes were tightly regulated by DAF-16. In addition, DAF-16 has differential preference for motifs when acting as an activator or repressor, which awaits experimental verification. TRANSMODIS is computationally efficient and robust, making it a useful probabilistic framework for finding immediate targets. Public Library of Science 2008-03-19 /pmc/articles/PMC2266795/ /pubmed/18350157 http://dx.doi.org/10.1371/journal.pone.0001821 Text en Yu et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Yu, Ron X. Liu, Jie True, Nick Wang, Wei Identification of Direct Target Genes Using Joint Sequence and Expression Likelihood with Application to DAF-16 |
title | Identification of Direct Target Genes Using Joint Sequence and Expression Likelihood with Application to DAF-16 |
title_full | Identification of Direct Target Genes Using Joint Sequence and Expression Likelihood with Application to DAF-16 |
title_fullStr | Identification of Direct Target Genes Using Joint Sequence and Expression Likelihood with Application to DAF-16 |
title_full_unstemmed | Identification of Direct Target Genes Using Joint Sequence and Expression Likelihood with Application to DAF-16 |
title_short | Identification of Direct Target Genes Using Joint Sequence and Expression Likelihood with Application to DAF-16 |
title_sort | identification of direct target genes using joint sequence and expression likelihood with application to daf-16 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2266795/ https://www.ncbi.nlm.nih.gov/pubmed/18350157 http://dx.doi.org/10.1371/journal.pone.0001821 |
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