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    The 3'-to-5' exoribonuclease Nibbler shapes the 3' ends of microRNAs bound to Drosophila Argonaute1

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    Authors
    Han, Bo W.
    Hung, Jui-Hung
    Weng, Zhiping
    Zamore, Phillip D.
    Ameres, Stefan L.
    UMass Chan Affiliations
    Department of Biochemistry and Molecular Pharmacology
    Program in Bioinformatics and Integrative Biology
    Document Type
    Journal Article
    Publication Date
    2011-11-22
    Keywords
    Animals
    Argonaute Proteins
    Cell Line
    Drosophila Proteins
    Drosophila melanogaster
    Exoribonucleases
    MicroRNAs
    Polymerase Chain Reaction
    RNA Helicases
    *RNA Interference
    *RNA Processing, Post-Transcriptional
    RNA, Messenger
    RNA-Induced Silencing Complex
    Ribonuclease III
    Animal Experimentation and Research
    Bioinformatics
    Genetics and Genomics
    Molecular Biology
    Nucleic Acids, Nucleotides, and Nucleosides
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    Link to Full Text
    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3236499/
    Abstract
    BACKGROUND: MicroRNAs (miRNAs) are ~22 nucleotide (nt) small RNAs that control development, physiology, and pathology in animals and plants. Production of miRNAs involves the sequential processing of primary hairpin-containing RNA polymerase II transcripts by the RNase III enzymes Drosha in the nucleus and Dicer in the cytoplasm. miRNA duplexes then assemble into Argonaute proteins to form the RNA-induced silencing complex (RISC). In mature RISC, a single-stranded miRNA directs the Argonaute protein to bind partially complementary sequences, typically in the 3' untranslated regions of messenger RNAs, repressing their expression. RESULTS: Here, we show that after loading into Argonaute1 (Ago1), more than a quarter of all Drosophila miRNAs undergo 3' end trimming by the 3'-to-5' exoribonuclease Nibbler (CG9247). Depletion of Nibbler by RNA interference (RNAi) reveals that miRNAs are frequently produced by Dicer-1 as intermediates that are longer than ~22 nt. Trimming of miRNA 3' ends occurs after removal of the miRNA* strand from pre-RISC and may be the final step in RISC assembly, ultimately enhancing target messenger RNA repression. In vivo, depletion of Nibbler by RNAi causes developmental defects. CONCLUSIONS: We provide a molecular explanation for the previously reported heterogeneity of miRNA 3' ends and propose a model in which Nibbler converts miRNAs into isoforms that are compatible with the preferred length of Ago1-bound small RNAs.
    Source

    Curr Biol. 2011 Nov 22;21(22):1878-87. doi: 10.1016/j.cub.2011.09.034. Link to article on publisher's site

    DOI
    10.1016/j.cub.2011.09.034
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/25878
    PubMed ID
    22055293
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    Link to Article in PubMed

    ae974a485f413a2113503eed53cd6c53
    10.1016/j.cub.2011.09.034
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