Kinetochores distinguish GTP from GDP forms of the microtubule lattice

Article

关键词: SLOWLY HYDROLYZABLE ANALOG;    NEWT LUNG-CELLS;    DYNAMIC INSTABILITY;    BUDDING YEAST;    MITOTIC SPINDLE;    PROTEIN COMPLEX;    LIVING CELLS;    IN-VITRO;    CENTROMERE;    HYDROLYSIS;   

DOI  :  10.1038/42270

来源: SCIE

【 摘 要 】

During prometaphase in mitotic cell division, chromosomes attach to the walls of microtubules and subsequently move to microtubule ends, where they stay throughout mitosis(1,2). This end-attachment seems to be essential for correct chromosome segregating. However, the mechanism by which kinetochores, the multiprotein complexes that link chromosomes to the microtubules of the mitotic spindle(3,4), recognize and stay attached to microtubule ends is not understood. One due comes from the hydrolysis of GTP that occurs during microtubule polymerization. Although tubulin dimers must contain GTP to polymerize, this GTP is rapidly hydrolysed following the addition of dimers to a growing polymer. This creates a microtubule consisting largely of GDP-tubulin, with a small cap of GTP-tubulin at the ends. It is possible that kinetochores distinguish the different structural states of a GTP-versus a GDP-microtubule lattice, We have examined this question in vitro using reconstituted kinetochores from the yeast Saccharomyces cerevisiae. We found that kinetochores in vitro bind preferentially to GTP-rather than GDP-microtubules, and to the plus-end preferentially over the lattice. Our results could explain how kinetochores stay at microtubule ends and thus segregate chromosomes correctly during mitosis in vivo. This result demonstrates that proteins exist that can distinguish the GTP conformation of the microtubule lattice.

【 授权许可】

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