During the prometaphase stage of mitosis, the cell builds a bipolar spindle of microtubules that mechanically segregates sister chromatids between two daughter cells in anaphase. The spindle assembly checkpoint (SAC) is a quality control mechanism that monitors proper attachment of microtubules to chromosome kinetochores during prometaphase. Segregation occurs only when each chromosome is bi-oriented with each kinetochore pair attached to microtubules emanating from opposite spindle poles. Overexpression of the protein kinase Aurora A is a feature of various cancers and is thought to enable tumour cells to bypass the SAC, leading to aneuploidy. Here, we took advantage of a chemical and chemical-genetic approach to specifically inhibit Aurora A kinase activity in late prometaphase. We observed that a loss of Aurora A activity directly affects SAC function, that Aurora A is essential for maintaining the checkpoint protein Mad2 on unattached kinetochores and that inhibition of Aurora A leads to loss of the SAC, even in the presence of nocodazole or Taxol. This is a new finding that should affect the way Aurora A inhibitors are used in cancer treatments.
机构:
Wellcome Trust Centre for Cell Biology, University of Edinburgh, King's Buildings
Centre National de la Recherche Scientifique, Pierre Fabre UMR 2587, 31400 ToulouseWellcome Trust Centre for Cell Biology, University of Edinburgh, King's Buildings
Haren L.
Gnadt N.
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Wellcome Trust Centre for Cell Biology, University of Edinburgh, King's BuildingsWellcome Trust Centre for Cell Biology, University of Edinburgh, King's Buildings
Gnadt N.
Wright M.
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Centre National de la Recherche Scientifique, Pierre Fabre UMR 2587, 31400 ToulouseWellcome Trust Centre for Cell Biology, University of Edinburgh, King's Buildings
Wright M.
Merdes A.
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Wellcome Trust Centre for Cell Biology, University of Edinburgh, King's Buildings
Centre National de la Recherche Scientifique, Pierre Fabre UMR 2587, 31400 ToulouseWellcome Trust Centre for Cell Biology, University of Edinburgh, King's Buildings
机构:
UCL, Oocyte & Embryo Res Lab, Dept Cell & Dev Biol, Div Biosci, London, EnglandUCL, Oocyte & Embryo Res Lab, Dept Cell & Dev Biol, Div Biosci, London, England
Homer, Hayden
Gui, Liming
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机构:UCL, Oocyte & Embryo Res Lab, Dept Cell & Dev Biol, Div Biosci, London, England
Gui, Liming
Carroll, John
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机构:UCL, Oocyte & Embryo Res Lab, Dept Cell & Dev Biol, Div Biosci, London, England