Environmentally Induced Foregut Remodeling by PHA-4/FoxA and DAF-12/NHR.

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Bibliographic Details
Title: Environmentally Induced Foregut Remodeling by PHA-4/FoxA and DAF-12/NHR.
Authors: Ao, Wanyuan, Caudet, Jeb, Kent, W. James, Muttumu, Srikanth, Mango, Susan E.
Source: Science (pre-March 2025). 9/17/2004, Vol. 305 Issue 5691, p1743-1746. 4p. 2 Charts.
Subjects: Genetics, Information science, Heredity, Rheology, Computers in medicine, Genomes
Abstract: Growth and development of the Caenorhabditis etegans 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 pharyngeat 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. [ABSTRACT FROM AUTHOR]
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Database: Psychology and Behavioral Sciences Collection
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Abstract:Growth and development of the Caenorhabditis etegans 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 pharyngeat 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. [ABSTRACT FROM AUTHOR]
ISSN:00368075