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Meiotic nuclear pore complex remodeling provides key insights into nuclear basket organization.

Grant A KingRahel WettsteinJoseph M VarbergKeerthana ChetlapalliMadison E WalshLudovic C J GilletClaudia Hernández-ArmentaPedro BeltraoRuedi AebersoldSue L JaspersenJoao MatosElçin Ünal
Published in: The Journal of cell biology (2022)
Nuclear pore complexes (NPCs) are large proteinaceous assemblies that mediate nuclear compartmentalization. NPCs undergo large-scale structural rearrangements during mitosis in metazoans and some fungi. However, our understanding of NPC remodeling beyond mitosis remains limited. Using time-lapse fluorescence microscopy, we discovered that NPCs undergo two mechanistically separable remodeling events during budding yeast meiosis in which parts or all of the nuclear basket transiently dissociate from the NPC core during meiosis I and II, respectively. Meiosis I detachment, observed for Nup60 and Nup2, is driven by Polo kinase-mediated phosphorylation of Nup60 at its interface with the Y-complex. Subsequent reattachment of Nup60-Nup2 to the NPC core is facilitated by a lipid-binding amphipathic helix in Nup60. Preventing Nup60-Nup2 reattachment causes misorganization of the entire nuclear basket in gametes. Strikingly, meiotic nuclear basket remodeling also occurs in the distantly related fission yeast, Schizosaccharomyces pombe. Our study reveals a conserved and developmentally programmed aspect of NPC plasticity, providing key mechanistic insights into the nuclear basket organization.
Keyphrases
  • high resolution
  • transcription factor
  • optical coherence tomography
  • single cell
  • energy transfer