How the kinetochore couples microtubule force and centromere stretch to move chromosomes.
dc.contributor.author | Suzuki, Aussie | |
dc.contributor.author | Badger, Benjamin L | |
dc.contributor.author | Haase, Julian | |
dc.contributor.author | Ohashi, Tomoo | |
dc.contributor.author | Erickson, Harold P | |
dc.contributor.author | Salmon, Edward D | |
dc.contributor.author | Bloom, Kerry | |
dc.date.accessioned | 2018-04-01T15:08:02Z | |
dc.date.available | 2018-04-01T15:08:02Z | |
dc.date.issued | 2016-04 | |
dc.date.updated | 2018-04-01T15:08:00Z | |
dc.description.abstract | The Ndc80 complex (Ndc80, Nuf2, Spc24 and Spc25) is a highly conserved kinetochore protein essential for end-on anchorage to spindle microtubule plus ends and for force generation coupled to plus-end polymerization and depolymerization. Spc24/Spc25 at one end of the Ndc80 complex binds the kinetochore. The N-terminal tail and CH domains of Ndc80 bind microtubules, and an internal domain binds microtubule-associated proteins (MAPs) such as the Dam1 complex. To determine how the microtubule- and MAP-binding domains of Ndc80 contribute to force production at the kinetochore in budding yeast, we have inserted a FRET tension sensor into the Ndc80 protein about halfway between its microtubule-binding and internal loop domains. The data support a mechanical model of force generation at metaphase where the position of the kinetochore relative to the microtubule plus end reflects the relative strengths of microtubule depolymerization, centromere stretch and microtubule-binding interactions with the Ndc80 and Dam1 complexes. | |
dc.identifier.issn | 1465-7392 | |
dc.identifier.issn | 1476-4679 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | Springer Science and Business Media LLC | |
dc.relation.ispartof | Nature cell biology | |
dc.relation.isversionof | 10.1038/ncb3323 | |
dc.subject | Chromosomes, Fungal | |
dc.subject | Centromere | |
dc.subject | Kinetochores | |
dc.subject | Microtubules | |
dc.subject | Saccharomycetales | |
dc.subject | Cell Cycle Proteins | |
dc.subject | Microtubule-Associated Proteins | |
dc.subject | Saccharomyces cerevisiae Proteins | |
dc.subject | Luminescent Proteins | |
dc.subject | Nuclear Proteins | |
dc.subject | Microscopy, Fluorescence | |
dc.subject | Fluorescence Resonance Energy Transfer | |
dc.subject | Binding Sites | |
dc.subject | Protein Binding | |
dc.subject | Kinetics | |
dc.subject | Mutation | |
dc.subject | Models, Biological | |
dc.subject | Time-Lapse Imaging | |
dc.title | How the kinetochore couples microtubule force and centromere stretch to move chromosomes. | |
dc.type | Journal article | |
duke.contributor.orcid | Erickson, Harold P|0000-0002-9104-8987 | |
pubs.issue | 4 | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | Duke | |
pubs.organisational-group | Duke Cancer Institute | |
pubs.organisational-group | Institutes and Centers | |
pubs.organisational-group | Biochemistry | |
pubs.organisational-group | Basic Science Departments | |
pubs.organisational-group | Cell Biology | |
pubs.publication-status | Published | |
pubs.volume | 18 |
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