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Non-centrosomal nucleation mediated by augmin organizes microtubules in post-mitotic neurons and controls axonal microtubule polarity

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  • Carlos Sánchez-Huertas

    (Institute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology
    Present address: Centre de Recherche en Biologie Cellulaire de Montpellier, CRBM-CNRS, UMR5237 Montpellier, France.)

  • Francisco Freixo

    (Institute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology)

  • Ricardo Viais

    (Institute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology)

  • Cristina Lacasa

    (Institute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology)

  • Eduardo Soriano

    (Physiology and Immunology, Faculty of Biology and INUB, University of Barcelona
    Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), ISCIII
    Vall d'Hebron Institute of Research
    Institució Catalana de Recerca i Estudis Avançats (ICREA))

  • Jens Lüders

    (Institute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology)

Abstract

Neurons display a highly polarized microtubule network that mediates trafficking throughout the extensive cytoplasm and is crucial for neuronal differentiation and function. In newborn migrating neurons, the microtubule network is organized by the centrosome. During neuron maturation, however, the centrosome gradually loses this activity, and how microtubules are organized in more mature neurons remains poorly understood. Here, we demonstrate that microtubule organization in post-mitotic neurons strongly depends on non-centrosomal nucleation mediated by augmin and by the nucleator γTuRC. Disruption of either complex not only reduces microtubule density but also microtubule bundling. These microtubule defects impair neurite formation, interfere with axon specification and growth, and disrupt axonal trafficking. In axons augmin does not merely mediate nucleation of microtubules but ensures their uniform plus end-out orientation. Thus, the augmin-γTuRC module, initially identified in mitotic cells, may be commonly used to generate and maintain microtubule configurations with specific polarity.

Suggested Citation

  • Carlos Sánchez-Huertas & Francisco Freixo & Ricardo Viais & Cristina Lacasa & Eduardo Soriano & Jens Lüders, 2016. "Non-centrosomal nucleation mediated by augmin organizes microtubules in post-mitotic neurons and controls axonal microtubule polarity," Nature Communications, Nature, vol. 7(1), pages 1-14, November.
  • Handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms12187
    DOI: 10.1038/ncomms12187
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    Cited by:

    1. Erik Zupa & Martin Würtz & Annett Neuner & Thomas Hoffmann & Mandy Rettel & Anna Böhler & Bram J. A. Vermeulen & Sebastian Eustermann & Elmar Schiebel & Stefan Pfeffer, 2022. "The augmin complex architecture reveals structural insights into microtubule branching," Nature Communications, Nature, vol. 13(1), pages 1-14, December.

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