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    Adaptive Evolution Leads to Cross-Species Incompatibility in the piRNA Transposon Silencing Machinery

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    Authors
    Parhad, Swapnil S.
    Tu, Shikui
    Weng, Zhiping
    Theurkauf, William E.
    UMass Chan Affiliations
    Department of Biochemistry and Molecular Pharmacology
    Program in Bioinformatics and Integrative Biology
    Program in Molecular Medicine
    Document Type
    Journal Article
    Publication Date
    2017-10-09
    Keywords
    adaptive evolution
    chromatin
    piRNA
    reproductive isolation
    transposon silencing
    Biochemistry, Biophysics, and Structural Biology
    Bioinformatics
    Computational Biology
    Developmental Biology
    Ecology and Evolutionary Biology
    Integrative Biology
    Systems Biology
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    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5653967/
    Abstract
    Reproductive isolation defines species divergence and is linked to adaptive evolution of hybrid incompatibility genes. Hybrids between Drosophila melanogaster and Drosophila simulans are sterile, and phenocopy mutations in the PIWI interacting RNA (piRNA) pathway, which silences transposons and shows pervasive adaptive evolution, and Drosophila rhino and deadlock encode rapidly evolving components of a complex that binds to piRNA clusters. We show that Rhino and Deadlock interact and co-localize in simulans and melanogaster, but simulans Rhino does not bind melanogaster Deadlock, due to substitutions in the rapidly evolving Shadow domain. Significantly, a chimera expressing the simulans Shadow domain in a melanogaster Rhino backbone fails to support piRNA production, disrupts binding to piRNA clusters, and leads to ectopic localization to bulk heterochromatin. Fusing melanogaster Deadlock to simulans Rhino, by contrast, restores localization to clusters. Deadlock binding thus directs Rhino to piRNA clusters, and Rhino-Deadlock co-evolution has produced cross-species incompatibilities, which may contribute to reproductive isolation.
    Source
    Dev Cell. 2017 Oct 9;43(1):60-70.e5. doi: 10.1016/j.devcel.2017.08.012. Epub 2017 Sep 14. Link to article on publisher's site
    DOI
    10.1016/j.devcel.2017.08.012
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/25830
    PubMed ID
    28919205
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    ae974a485f413a2113503eed53cd6c53
    10.1016/j.devcel.2017.08.012
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