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      Dynamic maintenance of asymmetric meiotic spindle position through Arp2/3-complex-driven cytoplasmic streaming in mouse oocytes.

      Nature cell biology
      Actin Cytoskeleton, drug effects, metabolism, Actin-Related Protein 2, genetics, Actin-Related Protein 2-3 Complex, antagonists & inhibitors, Actin-Related Protein 3, Animals, Cells, Cultured, Cytoplasmic Streaming, Female, Fourier Analysis, Heterocyclic Compounds with 4 or More Rings, pharmacology, Indoles, Kymography, Meiosis, Mice, Microscopy, Confocal, Microscopy, Video, Morpholinos, Myosin Type II, Nocodazole, Oocytes, Protein Transport, Recombinant Fusion Proteins, Spindle Apparatus, Time Factors, ran GTP-Binding Protein

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          Abstract

          Mature mammalian oocytes are poised for completing meiosis II (MII) on fertilization by positioning the spindle close to an actomyosin-rich cortical cap. Here, we show that the Arp2/3 complex localizes to the cortical cap in a Ran-GTPase-dependent manner and nucleates actin filaments in the cortical cap and a cytoplasmic actin network. Inhibition of Arp2/3 activity leads to rapid dissociation of the spindle from the cortex. Live-cell imaging and spatiotemporal image correlation spectroscopy analysis reveal that actin filaments flow continuously away from the Arp2/3-rich cortex, driving a cytoplasmic streaming expected to exert a net pushing force on the spindle towards the cortex. Arp2/3 inhibition not only diminishes this actin flow and cytoplasmic streaming but also enables a reverse streaming driven by myosin-II-based cortical contraction, moving the spindle away from the cortex. Thus, the asymmetric MII spindle position is dynamically maintained as a result of balanced forces governed by the Arp2/3 complex.

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