FB2026_02 , released June 18, 2026
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Lee, S.K., Shen, W., Wen, W., Joo, Y., Xue, Y., Park, A., Qiang, A., Su, S., Zhang, T., Zhang, M., Fan, J., Zhang, Y., De, S., Gainetdinov, I., Sharov, A., Maragkakis, M., Wang, W. (2025). Topoisomerase 3b facilitates piRNA biogenesis to promote transposon silencing and germ cell development.  Cell Rep. 44(4): 115495.
FlyBase ID
FBrf0262201
Publication Type
Research paper
Abstract
Topoisomerases typically function in the nucleus to relieve topological stress in DNA. Here, we show that a dual-activity topoisomerase, Top3b, and its partner, TDRD3, largely localize in the cytoplasm and interact biochemically and genetically with PIWI-interacting RNA (piRNA) processing enzymes to promote piRNA biogenesis, post-transcriptional gene silencing (PTGS) of transposons, and Drosophila germ cell development. Top3b requires its topoisomerase activity to promote PTGS of a transposon reporter and preferentially silences long and highly expressed transposons, suggesting that RNAs with these features may produce more topological stress for topoisomerases to solve. The double mutants between Top3b and piRNA processing enzymes exhibit stronger disruption of the signatures and levels of germline piRNAs, more de-silenced transposons, and larger defects in germ cells than either single mutant. Our data suggest that Top3b can act in an RNA-based process-piRNA biogenesis and PTGS of transposons-and this function is required for Top3b to promote normal germ cell function.
PubMed ID
PubMed Central ID
PMC12070812 (PMC) (EuropePMC)
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Assignment of cell line based on information provided by the author in the Fast Track Your Paper tool.
FlyBase Curators, 2020-, Assignment of cell line based on information provided by the author in the Fast Track Your Paper tool. [FBrf0247694]

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    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Cell Rep.
    Title
    Cell reports
    ISBN/ISSN
    2211-1247
    Data From Reference
    Aberrations (1)
    Alleles (20)
    Genes (11)
    Physical Interactions (12)
    Cell Lines (1)
    Insertions (3)
    Experimental Tools (1)
    Transgenic Constructs (7)