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Kinetochore microtubule dynamics and attachment stability are regulated by Hec1

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Musacchio,  Andrea
Abt. I:Mechanistische Zellbiologie, Max Planck Institute of Molecular Physiology, Max Planck Society;

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引用

DeLuca, J. G., Gall, W. E., Ciferri, C., Cimini, D., Musacchio, A., & Salmon, E. D. (2006). Kinetochore microtubule dynamics and attachment stability are regulated by Hec1. CELL, 127(5), 969-982. doi:10.1016/j.cell.2006.09.047.


引用: https://hdl.handle.net/11858/00-001M-0000-0015-3B00-5
要旨
Mitotic cells face the challenging tasks of linking kinetochores to growing and, shortening microtubules and actively regulating these dynamic attachments to produce accurate chromosome segregation. We report here that Ndc80/Hec1 functions in regulating kinetochore microtubule plus-end dynamics and attachment stability. Microinjection of an antibody to the N terminus of Hec1 suppresses both microtubule detachment and microtubule plus-end polymerization and depolymerization at kinetochores of PtK1 cells. Centromeres become hyperstretched, kinetochore fibers shorten from spindle poles, kinetochore microtubule attachment errors increase, and chromosomes severely mis-segregate. The N terminus of Hec1 is phosphorylated by Aurora B kinase in vitro, and cells expressing N-terminal nonphosphorylatable mutants of Hec1 exhibit an increase in merotelic attachments, hyperstretching of centromeres, and errors in chromosome segregation. These findings reveal a key role for the Hec1 N terminus in controlling dynamic behavior of kinetochore microtubules.