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A gene-centered C. elegans protein-DNA interaction network
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4506897
Author(s) Deplancke, Bart; Mukhopadhyay, Arnab; Ao, Wanyuan; Elewa, Ahmed M.; Grove, Christian A.; Martinez, Natalia J.; Sequerra, Reynaldo; Doucette-Stamm, Lynn; Reece-Hoyes, John S.; Hope, Ian A.; Tissenbaum, Heidi A.; Mango, Susan E.; Walhout, Albertha J. M.
Author(s) at UniBasel Mango, Susan Elizabeth
Year 2006
Title A gene-centered C. elegans protein-DNA interaction network
Journal Cell
Volume 125
Number 6
Pages / Article-Number 1193-1205
Mesh terms Animals; Caenorhabditis elegans, genetics, metabolism; Caenorhabditis elegans Proteins, genetics, metabolism; Computational Biology; DNA, Helminth, metabolism; DNA-Binding Proteins, genetics, metabolism; Digestive System, metabolism; Promoter Regions, Genetic; Regulatory Elements, Transcriptional; Saccharomyces cerevisiae, genetics; Transcription Factors, metabolism; Transcription, Genetic; Two-Hybrid System Techniques
Abstract Transcription regulatory networks consist of physical and functional interactions between transcription factors (TFs) and their target genes. The systematic mapping of TF-target gene interactions has been pioneered in unicellular systems, using "TF-centered" methods (e.g., chromatin immunoprecipitation). However, metazoan systems are less amenable to such methods. Here, we used "gene-centered" high-throughput yeast one-hybrid (Y1H) assays to identify 283 interactions between 72 C. elegans digestive tract gene promoters and 117 proteins. The resulting protein-DNA interaction (PDI) network is highly connected and enriched for TFs that are expressed in the digestive tract. We provide functional annotations for approximately 10% of all worm TFs, many of which were previously uncharacterized, and find ten novel putative TFs, illustrating the power of a gene-centered approach. We provide additional in vivo evidence for multiple PDIs and illustrate how the PDI network provides insights into metazoan differential gene expression at a systems level.
Publisher Cell Press
ISSN/ISBN 0092-8674 ; 1097-4172
edoc-URL https://edoc.unibas.ch/70584/
Full Text on edoc No
Digital Object Identifier DOI 10.1016/j.cell.2006.04.038
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/16777607
ISI-Number WOS:000238602700022
Document type (ISI) Article
 
   

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