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Centrosomal ALIX regulates mitotic spindle orientation by modulating astral microtubule dynamics
Authors:Lene Malerød  Åsmund Husabø Eikenes  Andreas Brech  Knut Liestøl  Harald Stenmark  Kaisa Haglund
Affiliation:1. Department of Molecular Cell Biology, Institute for Cancer Research, Oslo University Hospital, Oslo, Norway;2. Centre for Cancer Cell Reprogramming, Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway;3. Department of Informatics, University of Oslo, Oslo, Norway
Abstract:The orientation of the mitotic spindle (MS) is tightly regulated, but the molecular mechanisms are incompletely understood. Here we report a novel role for the multifunctional adaptor protein ALG‐2‐interacting protein X (ALIX) in regulating MS orientation in addition to its well‐established role in cytokinesis. We show that ALIX is recruited to the pericentriolar material (PCM) of the centrosomes and promotes correct orientation of the MS in asymmetrically dividing Drosophila stem cells and epithelial cells, and symmetrically dividing Drosophila and human epithelial cells. ALIX‐deprived cells display defective formation of astral microtubules (MTs), which results in abnormal MS orientation. Specifically, ALIX is recruited to the PCM via Drosophila Spindle defective 2 (DSpd‐2)/Cep192, where ALIX promotes accumulation of γ‐tubulin and thus facilitates efficient nucleation of astral MTs. In addition, ALIX promotes MT stability by recruiting microtubule‐associated protein 1S (MAP1S), which stabilizes newly formed MTs. Altogether, our results demonstrate a novel evolutionarily conserved role of ALIX in providing robustness to the orientation of the MS by promoting astral MT formation during asymmetric and symmetric cell division.
Keywords:   ALIX     MAP1S  microtubule  mitotic spindle orientation  γ  ‐tubulin
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