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    Maelstrom Represses Canonical Polymerase II Transcription within Bi-directional piRNA Clusters in Drosophila melanogaster

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    Authors
    Chang, Timothy
    Mattei, Eugenio
    Colpan, Cansu
    Weng, Zhiping
    Zamore, Phillip D.
    UMass Chan Affiliations
    Graduate School of Biomedical Sciences
    Department of Biochemistry and Molecular Pharmacology
    Program in Bioinformatics and Integrative Biology
    RNA Therapeutics Institute
    Document Type
    Journal Article
    Publication Date
    2018-11-12
    Keywords
    Argonaute
    Armitage
    Maelstrom
    PIWI-interacting RNA
    Piwi
    Rhino
    piRNA
    small silencing RNA
    transcription
    transposon
    Amino Acids, Peptides, and Proteins
    Biochemistry
    Bioinformatics
    Computational Biology
    Genetics and Genomics
    Molecular Biology
    Nucleic Acids, Nucleotides, and Nucleosides
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    Link to Full Text
    https://doi.org/10.1016/j.molcel.2018.10.038
    Abstract
    In Drosophila, 23-30 nt long PIWI-interacting RNAs (piRNAs) direct the protein Piwi to silence germline transposon transcription. Most germline piRNAs derive from dual-strand piRNA clusters, heterochromatic transposon graveyards that are transcribed from both genomic strands. These piRNA sources are marked by the heterochromatin protein 1 homolog Rhino (Rhi), which facilitates their promoter-independent transcription, suppresses splicing, and inhibits transcriptional termination. Here, we report that the protein Maelstrom (Mael) represses canonical, promoter-dependent transcription in dual-strand clusters, allowing Rhi to initiate piRNA precursor transcription. Mael also represses promoter-dependent transcription at sites outside clusters. At some loci, Mael repression requires the piRNA pathway, while at others, piRNAs play no role. We propose that by repressing canonical transcription of individual transposon mRNAs, Mael helps Rhi drive non-canonical transcription of piRNA precursors without generating mRNAs encoding transposon proteins.
    Source

    Mol Cell. 2018 Nov 12. pii: S1097-2765(18)30932-8. doi: 10.1016/j.molcel.2018.10.038. [Epub ahead of print]. Link to article on publisher's site

    DOI
    10.1016/j.molcel.2018.10.038
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/25850
    PubMed ID
    30527661
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    Link to Article in PubMed

    ae974a485f413a2113503eed53cd6c53
    10.1016/j.molcel.2018.10.038
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    Program in Bioinformatics and Integrative Biology Publications

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