FB2026_02 , released June 18, 2026
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Citation
Crawford, B.I., Talley, M.J., Russman, J., Riddle, J., Torres, S., Williams, T., Longworth, M.S. (2024). Condensin-mediated restriction of retrotransposable elements facilitates brain development in Drosophila melanogaster.  Nat. Commun. 15(1): 2716.
FlyBase ID
FBrf0259152
Publication Type
Research paper
Abstract
Neural stem and progenitor cell (NSPC) maintenance is essential for ensuring that organisms are born with proper brain volumes and head sizes. Microcephaly is a disorder in which babies are born with significantly smaller head sizes and cortical volumes. Mutations in subunits of the DNA organizing complex condensin have been identified in microcephaly patients. However, the molecular mechanisms by which condensin insufficiency causes microcephaly remain elusive. We previously identified conserved roles for condensins in repression of retrotransposable elements (RTEs). Here, we show that condensin subunit knockdown in NSPCs of the Drosophila larval central brain increases RTE expression and mobility which causes cell death, and significantly decreases adult head sizes and brain volumes. These findings suggest that unrestricted RTE expression and activity may lead to improper brain development in condensin insufficient organisms, and lay the foundation for future exploration of causative roles for RTEs in other microcephaly models.
PubMed ID
PubMed Central ID
PMC10978865 (PMC) (EuropePMC)
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Erratum

Author Correction: Condensin-mediated restriction of retrotransposable elements facilitates brain development in Drosophila melanogaster.
Crawford et al., 2025, Nat. Commun. 16(1): 933 [FBrf0261508]

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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Nat. Commun.
    Title
    Nature communications
    ISBN/ISSN
    2041-1723
    Data From Reference
    Chemicals (2)
    Genes (5)
    Human Disease Models (1)