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    A single Argonaute protein mediates both transcriptional and posttranscriptional silencing in Schizosaccharomyces pombe

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    Authors
    Sigova, Alla A.
    Rhind, Nicholas R.
    Zamore, Phillip D.
    UMass Chan Affiliations
    Department of Biochemistry and Molecular Pharmacology
    Document Type
    Journal Article
    Publication Date
    2004-09-17
    Keywords
    Base Sequence; DNA Primers; Flow Cytometry; Gene Silencing; Green Fluorescent Proteins; Luminescent Proteins; Schizosaccharomyces; Schizosaccharomyces pombe Proteins; Transcription, Genetic
    Life Sciences
    Medicine and Health Sciences
    
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    Link to Full Text
    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC522986/
    Abstract
    The Schizosaccharomyces pombe genome encodes only one of each of the three major classes of proteins implicated in RNA silencing: Dicer (Dcr1), RNA-dependent RNA polymerase (RdRP; Rdp1), and Argonaute (Ago1). These three proteins are required for silencing at centromeres and for the initiation of transcriptionally silent heterochromatin at the mating-type locus. Here, we show that the introduction of a double-stranded RNA (dsRNA) hairpin corresponding to a green fluorescent protein (GFP) transgene triggers classical RNA interference (RNAi) in S. pombe. That is, GFP silencing triggered by dsRNA reflects a change in the steady-state concentration of GFP mRNA, but not in the rate of GFP transcription. RNAi in S. pombe requires dcr1, rdp1, and ago1, but does not require chp1, tas3, or swi6, genes required for transcriptional silencing. Thus, the RNAi machinery in S. pombe can direct both transcriptional and posttranscriptional silencing using a single Dicer, RdRP, and Argonaute protein. Our findings suggest that these three proteins fulfill a common biochemical function in distinct siRNA-directed silencing pathways.
    Source

    Genes Dev. 2004 Oct 1;18(19):2359-67. Epub 2004 Sep 15. Link to article on publisher's site

    DOI
    10.1101/gad.1218004
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/32554
    PubMed ID
    15371329
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    Link to Article in PubMed

    ae974a485f413a2113503eed53cd6c53
    10.1101/gad.1218004
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