Direct induction of microtubule branching by microtubule nucleation factor SSNA1

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Basnet, Nirakar | Nedozralova, Hana | Crevenna, Alvaro, H | Bodakuntla, Satish | Schlichthaerle, Thomas | Taschner, Michael | Cardone, Giovanni | Janke, Carsten | Jungmann, Ralf | Magiera, Maria, M | Biertümpfel, Christian | Mizuno, Naoko

Edité par CCSD ; Nature Publishing Group -

International audience. Microtubules are central elements of the eukaryotic cytoskeleton that often function as part of branched networks. Current models for branching include nucleation of new microtubules from severed microtubule seeds or from gamma-tubulin recruited to the side of a pre-existing microtubule. Here, we found that microtubules can be directly remodeled into branched structures by the microtubule-remodeling factor SSNA1 (or also NA14/DIP13). The branching activity of SSNA1 relies on its ability to self-assemble into fibrils in a head-to-tail fashion. SSNA1 fibrils guide protofilaments of a microtubule to split apart to form daughter microtubules. We further found that SSNA1 localizes at axon branching sites and has a key role in neuronal development. SSNA1 mutants that abolish microtubule branching in vitro also fail to promote axon development and branching when overexpressed in neurons. We have therefore, discovered a mechanism for microtubule-branching and implicated its role in neuronal development. Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:

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