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Citation
Sato, K., Iwasaki, Y.W., Shibuya, A., Carninci, P., Tsuchizawa, Y., Ishizu, H., Siomi, M.C., Siomi, H. (2015). Krimper Enforces an Antisense Bias on piRNA Pools by Binding AGO3 in the Drosophila Germline.  Mol. Cell 59(4): 553--563.
FlyBase ID
FBrf0229343
Publication Type
Research paper
Abstract
Piwi-interacting RNAs (piRNAs) suppress transposon activity in animal germ cells. In the Drosophila ovary, primary Aubergine (Aub)-bound antisense piRNAs initiate the ping-pong cycle to produce secondary AGO3-bound sense piRNAs. This increases the number of secondary Aub-bound antisense piRNAs that can act to destroy transposon mRNAs. Here we show that Krimper (Krimp), a Tudor-domain protein, directly interacts with piRNA-free AGO3 to promote symmetrical dimethylarginine (sDMA) modification, ensuring sense piRNA-loading onto sDMA-modified AGO3. In aub mutant ovaries, AGO3 associates with ping-pong signature piRNAs, suggesting AGO3's compatibility with primary piRNA loading. Krimp sequesters ectopically expressed AGO3 within Krimp bodies in cultured ovarian somatic cells (OSCs), in which only the primary piRNA pathway operates. Upon krimp-RNAi in OSCs, AGO3 loads with piRNAs, further showing the capacity of AGO3 for primary piRNA loading. We propose that Krimp enforces an antisense bias on piRNA pools by binding AGO3 and blocking its access to primary piRNAs.
Graphical Abstract
Obtained with permission from Cell Press.
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PubMed Central ID
Related Publication(s)
Note

Tudor-domain containing proteins act to make the piRNA pathways more robust in Drosophila.
Sato et al., 2015, Fly 9(2): 86--90 [FBrf0230667]

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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Mol. Cell
    Title
    Molecular Cell
    Publication Year
    1997-
    ISBN/ISSN
    1097-2765 1097-4164
    Data From Reference
    Genes (10)
    Physical Interactions (8)
    Cell Lines (1)
    Natural transposons (2)