The Dam1 kinetochore ring complex moves processively on depolymerizing microtubule ends
Stefan Westermann,
Hong-Wei Wang,
Agustin Avila-Sakar,
David G. Drubin,
Eva Nogales and
Georjana Barnes ()
Additional contact information
Stefan Westermann: Department of Molecular and Cell Biology
Hong-Wei Wang: Lawrence Berkeley National Laboratory
Agustin Avila-Sakar: Lawrence Berkeley National Laboratory
David G. Drubin: Department of Molecular and Cell Biology
Eva Nogales: Department of Molecular and Cell Biology
Georjana Barnes: Department of Molecular and Cell Biology
Nature, 2006, vol. 440, issue 7083, 565-569
Abstract:
Hang on in there A long-standing mystery of mitosis research is the mechanism that transports chromosomes to the nuclear-spindle poles during anaphase. The chromosomes seem to gain their objective by clinging on to the kinetochore microtubule polymers despite the fact that they are disassembling at the time. Fluorescence microscopy has now been used to produce movies and electron micrographs that show how it's done. The microtubule polymer disassembles via a conformational change that pushes the Dam1 ring complex, an important microtubule binding element in the budding yeast kinetochore, along its lattice. This elegant mechanism may be the key to the conversion of force generated by microtubule depolymerization into the chromosome movements seen in mitosis.
Date: 2006
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DOI: 10.1038/nature04409
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