Abstract
Growth and development of the Caenorhabditis elegans foregut (pharynx) depends on coordinated gene expression, mediated by pharynx defective (PHA)-4/FoxA in combination with additional, largely unidentified transcription factors. Here, we used whole genome analysis to establish clusters of genes expressed in different pharyngeal cell types. We created an expectation maximization algorithm to identify cis-regulatory elements that activate expression within the pharyngeal gene clusters. One of these elements mediates the response to environmental conditions within pharyngeal muscles and is recognized by the nuclear hormone receptor (NHR) DAF-12. Our data suggest that PHA-4 and DAF-12 endow the pharynx with transcriptional plasticity to respond to diverse developmental and physiological cues. Our combination of bioinformatics and in vivo analysis has provided a powerful means for genome-wide investigation of transcriptional control.
Publication types
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Caenorhabditis elegans / genetics*
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Caenorhabditis elegans / growth & development*
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Caenorhabditis elegans Proteins / genetics
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Caenorhabditis elegans Proteins / physiology*
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Computational Biology
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Enhancer Elements, Genetic
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Food
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Gene Expression Profiling
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Gene Expression Regulation, Developmental*
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Genes, Helminth*
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Genes, Regulator
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Larva / genetics
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Larva / growth & development
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Multigene Family
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Muscle Development
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Muscles / physiology
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Oligonucleotide Array Sequence Analysis
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Pharynx / cytology
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Pharynx / growth & development
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Pharynx / physiology
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Receptors, Cytoplasmic and Nuclear / genetics
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Receptors, Cytoplasmic and Nuclear / physiology*
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Regulatory Sequences, Nucleic Acid
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Trans-Activators / genetics
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Trans-Activators / physiology*
Substances
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Caenorhabditis elegans Proteins
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DAF-12 protein, C elegans
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Pha-4 protein, C elegans
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Receptors, Cytoplasmic and Nuclear
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Trans-Activators