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Local actin nucleation tunes centrosomal microtubule nucleation during passage through mitosis

    1. [1] University of Liverpool

      University of Liverpool

      Reino Unido

    2. [2] 1 MRC‐LMCB UCL London UK; 2 IPLS UCL London UK; 3 IFOM, the FIRC Institute of Molecular Oncology University of Milan Milan Italy; 4 University of Grenoble Grenoble France
    3. [3] 1 MRC‐LMCB UCL London UK; 2 IPLS UCL London UK
    4. [4] 3 IFOM, the FIRC Institute of Molecular Oncology University of Milan Milan Italy; 6 Department of Oncology and Hemato‐Oncology University of Milan Milan Italy
    5. [5] 7 Hospital Saint‐Louis Paris France
    6. [6] 4 University of Grenoble Grenoble France
  • Localización: EMBO journal: European Molecular Biology Organization, ISSN 0261-4189, Vol. 38, Nº. 11, 2019
  • Idioma: inglés
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  • Resumen
    • Cells going through mitosis undergo precisely timed changes in cell shape and organisation, which serve to ensure the fair partitioning of cellular components into the two daughter cells. These structural changes are driven by changes in actin filament and microtubule dynamics and organisation. While most evidence suggests that the two cytoskeletal systems are remodelled in parallel during mitosis, recent work in interphase cells has implicated the centrosome in both microtubule and actin nucleation, suggesting the potential for regulatory crosstalk between the two systems. Here, by using both in vitro and in vivo assays to study centrosomal actin nucleation as cells pass through mitosis, we show that mitotic exit is accompanied by a burst in cytoplasmic actin filament formation that depends on WASH and the Arp2/3 complex. This leads to the accumulation of actin around centrosomes as cells enter anaphase and to a corresponding reduction in the density of centrosomal microtubules. Taken together, these data suggest that the mitotic regulation of centrosomal WASH and the Arp2/3 complex controls local actin nucleation, which may function to tune the levels of centrosomal microtubules during passage through mitosis.


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