FB2025_01 , released February 20, 2025
Reference Report
Open Close
Reference
Citation
Torras-Llort, M., Medina-Giró, S., Escudero-Ferruz, P., Lipinszki, Z., Moreno-Moreno, O., Karman, Z., Przewloka, M.R., Azorín, F. (2020). A fraction of barrier-to-autointegration factor (BAF) associates with centromeres and controls mitosis progression.  Commun. Biol. 3(1): 454.
FlyBase ID
FBrf0246504
Publication Type
Research paper
Abstract
Barrier-to-Autointegration Factor (BAF) is a conserved nuclear envelope (NE) component that binds chromatin and helps its anchoring to the NE. Cycles of phosphorylation and dephosphorylation control BAF function. Entering mitosis, phosphorylation releases BAF from chromatin and facilitates NE-disassembly. At mitotic exit, PP2A-mediated dephosphorylation restores chromatin binding and nucleates NE-reassembly. Here, we show that in Drosophila a small fraction of BAF (cenBAF) associates with centromeres. We also find that PP4 phosphatase, which is recruited to centromeres by CENP-C, prevents phosphorylation and release of cenBAF during mitosis. cenBAF is necessary for proper centromere assembly and accurate chromosome segregation, being critical for mitosis progression. Disrupting cenBAF localization prevents PP2A inactivation in mitosis compromising global BAF phosphorylation, which in turn leads to its persistent association with chromatin, delays anaphase onset and causes NE defects. These results suggest that, together with PP4 and CENP-C, cenBAF forms a centromere-based mechanism that controls chromosome segregation and mitosis progression.
PubMed ID
PubMed Central ID
PMC7438335 (PMC) (EuropePMC)
Associated Information
Comments
Associated Files
Other Information
Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Commun. Biol.
    Title
    Communications biology
    ISBN/ISSN
    2399-3642
    Data From Reference
    Alleles (5)
    Genes (8)
    Physical Interactions (3)
    Cell Lines (1)
    Natural transposons (1)
    Insertions (4)
    Experimental Tools (2)
    Transgenic Constructs (4)