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Conserved Motifs and Prediction of Regulatory Modules in Caenorhabditis elegans

Transcriptional regulation, a primary mechanism for controlling the development of multicellular organisms, is carried out by transcription factors (TFs) that recognize and bind to their cognate binding sites. In Caenorhabditis elegans, our knowledge of which genes are regulated by which TFs, throug...

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Autores principales: Zhao, Guoyan, Ihuegbu, Nnamdi, Lee, Mo, Schriefer, Larry, Wang, Ting, Stormo, Gary D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3337475/
https://www.ncbi.nlm.nih.gov/pubmed/22540038
http://dx.doi.org/10.1534/g3.111.001081
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author Zhao, Guoyan
Ihuegbu, Nnamdi
Lee, Mo
Schriefer, Larry
Wang, Ting
Stormo, Gary D.
author_facet Zhao, Guoyan
Ihuegbu, Nnamdi
Lee, Mo
Schriefer, Larry
Wang, Ting
Stormo, Gary D.
author_sort Zhao, Guoyan
collection PubMed
description Transcriptional regulation, a primary mechanism for controlling the development of multicellular organisms, is carried out by transcription factors (TFs) that recognize and bind to their cognate binding sites. In Caenorhabditis elegans, our knowledge of which genes are regulated by which TFs, through binding to specific sites, is still very limited. To expand our knowledge about the C. elegans regulatory network, we performed a comprehensive analysis of the C. elegans, Caenorhabditis briggsae, and Caenorhabditis remanei genomes to identify regulatory elements that are conserved in all genomes. Our analysis identified 4959 elements that are significantly conserved across the genomes and that each occur multiple times within each genome, both hallmarks of functional regulatory sites. Our motifs show significant matches to known core promoter elements, TF binding sites, splice sites, and poly-A signals as well as many putative regulatory sites. Many of the motifs are significantly correlated with various types of experimental data, including gene expression patterns, tissue-specific expression patterns, and binding site location analysis as well as enrichment in specific functional classes of genes. Many can also be significantly associated with specific TFs. Combinations of motif occurrences allow us to predict the location of cis-regulatory modules and we show that many of them significantly overlap experimentally determined enhancers. We provide access to the predicted binding sites, their associated motifs, and the predicted cis-regulatory modules across the whole genome through a web-accessible database and as tracks for genome browsers.
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spelling pubmed-33374752012-04-26 Conserved Motifs and Prediction of Regulatory Modules in Caenorhabditis elegans Zhao, Guoyan Ihuegbu, Nnamdi Lee, Mo Schriefer, Larry Wang, Ting Stormo, Gary D. G3 (Bethesda) Investigations Transcriptional regulation, a primary mechanism for controlling the development of multicellular organisms, is carried out by transcription factors (TFs) that recognize and bind to their cognate binding sites. In Caenorhabditis elegans, our knowledge of which genes are regulated by which TFs, through binding to specific sites, is still very limited. To expand our knowledge about the C. elegans regulatory network, we performed a comprehensive analysis of the C. elegans, Caenorhabditis briggsae, and Caenorhabditis remanei genomes to identify regulatory elements that are conserved in all genomes. Our analysis identified 4959 elements that are significantly conserved across the genomes and that each occur multiple times within each genome, both hallmarks of functional regulatory sites. Our motifs show significant matches to known core promoter elements, TF binding sites, splice sites, and poly-A signals as well as many putative regulatory sites. Many of the motifs are significantly correlated with various types of experimental data, including gene expression patterns, tissue-specific expression patterns, and binding site location analysis as well as enrichment in specific functional classes of genes. Many can also be significantly associated with specific TFs. Combinations of motif occurrences allow us to predict the location of cis-regulatory modules and we show that many of them significantly overlap experimentally determined enhancers. We provide access to the predicted binding sites, their associated motifs, and the predicted cis-regulatory modules across the whole genome through a web-accessible database and as tracks for genome browsers. Genetics Society of America 2012-04-01 /pmc/articles/PMC3337475/ /pubmed/22540038 http://dx.doi.org/10.1534/g3.111.001081 Text en Copyright © 2012 Zhao et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Unported License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Zhao, Guoyan
Ihuegbu, Nnamdi
Lee, Mo
Schriefer, Larry
Wang, Ting
Stormo, Gary D.
Conserved Motifs and Prediction of Regulatory Modules in Caenorhabditis elegans
title Conserved Motifs and Prediction of Regulatory Modules in Caenorhabditis elegans
title_full Conserved Motifs and Prediction of Regulatory Modules in Caenorhabditis elegans
title_fullStr Conserved Motifs and Prediction of Regulatory Modules in Caenorhabditis elegans
title_full_unstemmed Conserved Motifs and Prediction of Regulatory Modules in Caenorhabditis elegans
title_short Conserved Motifs and Prediction of Regulatory Modules in Caenorhabditis elegans
title_sort conserved motifs and prediction of regulatory modules in caenorhabditis elegans
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3337475/
https://www.ncbi.nlm.nih.gov/pubmed/22540038
http://dx.doi.org/10.1534/g3.111.001081
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