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    ZNFX-1 Functions within Perinuclear Nuage to Balance Epigenetic Signals

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    Authors
    Ishidate, Takao
    Ozturk, Ahmet R.
    Durning, Daniel J.
    Sharma, Rita
    Shen, En-Zhi
    Chen, Hao
    Seth, Meetu
    Shirayama, Masaki
    Mello, Craig C.
    UMass Chan Affiliations
    Program in Bioinformatics and Integrative Biology
    RNA Therapeutics Institute
    Document Type
    Journal Article
    Publication Date
    2018-05-17
    Keywords
    Argonaute
    C. elegans
    CSR-1
    P-granule
    PIWI
    RNAa
    RNAe
    RdRP
    ZNFX-1
    nuage
    Amino Acids, Peptides, and Proteins
    Biochemistry, Biophysics, and Structural Biology
    Cell and Developmental Biology
    Genetic Phenomena
    Genetics and Genomics
    Nucleic Acids, Nucleotides, and Nucleosides
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    Link to Full Text
    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5994929/
    Abstract
    Animal cells have a remarkable capacity to adopt durable and heritable gene expression programs or epigenetic states that define the physical properties and diversity of somatic cell types. The maintenance of epigenetic programs depends on poorly understood pathways that prevent gain or loss of inherited signals. In the germline, epigenetic factors are enriched in liquid-like perinuclear condensates called nuage. Here, we identify the deeply conserved helicase-domain protein, ZNFX-1, as an epigenetic regulator and component of nuage that interacts with Argonaute systems to balance epigenetic inheritance. Our findings suggest that ZNFX-1 promotes the 3' recruitment of machinery that propagates the small RNA epigenetic signal and thus counteracts a tendency for Argonaute targeting to shift 5' along the mRNA. These functional insights support the idea that recently identified subdomains of nuage, including ZNFX-1 granules or "Z-granules," may define spatial and temporal zones of molecular activity during epigenetic regulation.
    Source

    Mol Cell. 2018 May 17;70(4):639-649.e6. doi: 10.1016/j.molcel.2018.04.009. Link to article on publisher's site

    DOI
    10.1016/j.molcel.2018.04.009
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/48843
    PubMed ID
    29775580
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    Link to Article in PubMed

    ae974a485f413a2113503eed53cd6c53
    10.1016/j.molcel.2018.04.009
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