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    Many transcription factors contribute to C. elegans growth and fat storage

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    Authors
    Mori, Akihiro
    Holdorf, Amy D.
    Walhout, Albertha J. M.
    UMass Chan Affiliations
    Program in Molecular Medicine
    Program in Systems Biology
    Document Type
    Journal Article
    Publication Date
    2017-09-01
    Keywords
    Cell and Developmental Biology
    Cellular and Molecular Physiology
    Genetics and Genomics
    Molecular Biology
    Systems Biology
    
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    Link to Full Text
    https://doi.org/10.1111/gtc.12516
    Abstract
    Reverse genetic screens by RNA interference (RNAi) in model organisms such as the nematode Caenorhabditis elegans have provided numerous insights into gene function, thereby connecting genotype to phenotype. However, genes that contribute only subtly are often missed because relatively large numbers of measurements and reliable quantification are required to overcome experimental and biological noise that may mask subtle phenotypic effects. Here, we address this challenge by focusing on two phenotypes in C. elegans: growth and fat storage. We carried out comprehensive RNAi knockdown of transcription factors (TFs), as these are known important regulators of biological processes during development and the maintenance of homeostasis. Microscopy images of TF knockdown animals stained with Oil Red O (ORO) were captured, and body size (proxy for growth) and ORO staining intensity (proxy for fat storage) were precisely quantified using a newly developed imaging tool we named IPPOME (Image Processing for Precise and Objective MEasurement). We found that a surprisingly large proportion of TFs contribute to growth and fat storage, but that most TFs have only subtle, yet significant effects. This study provides a blueprint for studies of other genes and phenotypes in C. elegans.
    Source

    Genes Cells. 2017 Sep;22(9):770-784. doi: 10.1111/gtc.12516. Epub 2017 Aug 8. Link to article on publisher's site

    DOI
    10.1111/gtc.12516
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/49842
    PubMed ID
    28791781
    Related Resources

    Link to Article in PubMed

    ae974a485f413a2113503eed53cd6c53
    10.1111/gtc.12516
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