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    The decapping scavenger enzyme DCS-1 controls microRNA levels in Caenorhabditis elegans

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    Authors
    Bosse, Gabriel D.
    Ruegger, Stefan
    Ow, Maria C.
    Vasquez-Rifo, Alejandro
    Rondeau, Evelyne L.
    Ambros, Victor R.
    Grosshans, Helge
    Simard, Martin J.
    UMass Chan Affiliations
    Program in Molecular Medicine
    Document Type
    Journal Article
    Publication Date
    2013-04-25
    Keywords
    Animals
    Caenorhabditis elegans
    Caenorhabditis elegans Proteins
    Exoribonucleases
    Gene Expression
    MicroRNAs
    Mutation
    N-Glycosyl Hydrolases
    RNA Interference
    RNA Stability
    RNA, Helminth
    RNA-Induced Silencing Complex
    Biochemistry
    Molecular Biology
    Molecular Genetics
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    Link to Full Text
    http://dx.doi.org/10.1016/j.molcel.2013.02.023
    Abstract
    In metazoans, microRNAs play a critical role in the posttranscriptional regulation of genes required for cell proliferation and differentiation. MicroRNAs themselves are regulated by a multitude of mechanisms influencing their transcription and posttranscriptional maturation. However, there is only sparse knowledge on pathways regulating the mature, functional form of microRNA. Here, we uncover the implication of the decapping scavenger protein DCS-1 in the control of microRNA turnover. In Caenorhabditis elegans, mutations in dcs-1 increase the levels of functional microRNAs. We demonstrate that DCS-1 interacts with the exonuclease XRN-1 to promote microRNA degradation in an independent manner from its known decapping scavenger activity, establishing two molecular functions for DCS-1. Our findings thus indicate that DCS-1 is part of a degradation complex that performs microRNA turnover in animals.
    Source
    Mol Cell. 2013 Apr 25;50(2):281-7. doi: 10.1016/j.molcel.2013.02.023. Epub 2013 Mar 28. Link to article on publisher's site
    DOI
    10.1016/j.molcel.2013.02.023
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/44432
    PubMed ID
    23541767
    Related Resources
    Link to Article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.molcel.2013.02.023
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