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dc.contributor.authorHowell, RSM
dc.contributor.authorCsikász-Nagy, A
dc.contributor.authorThorpe, PH
dc.date.accessioned2021-05-25T12:35:35Z
dc.date.available2019-05-02
dc.date.available2021-05-25T12:35:35Z
dc.date.issued2019-07-01
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/72065
dc.description.abstractThe yeast centrosome or Spindle Pole Body (SPB) is an organelle situated in the nuclear membrane, where it nucleates spindle microtubules and acts as a signaling hub. Various studies have explored the effects of forcing individual proteins to interact with the yeast SPB, however no systematic study has been performed. We used synthetic physical interactions to detect proteins that inhibit growth when forced to associate with the SPB. We found the SPB to be especially sensitive to relocalization, necessitating a novel data analysis approach. This novel analysis of SPI screening data shows that regions of the cell are locally more sensitive to forced relocalization than previously thought. Furthermore, we found a set of associations that result in elevated SPB number and, in some cases, multi-polar spindles. Since hyper-proliferation of centrosomes is a hallmark of cancer cells, these associations point the way for the use of yeast models in the study of spindle formation and chromosome segregation in cancer.en_US
dc.format.extent2183 - 2194
dc.languageeng
dc.relation.ispartofG3 (Bethesda)
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subjectSpindle Pole Bodyen_US
dc.subjectcentrosomeen_US
dc.subjectempirical Bayesen_US
dc.subjectlocalizationen_US
dc.titleSynthetic Physical Interactions with the Yeast Centrosome.en_US
dc.typeArticleen_US
dc.identifier.doi10.1534/g3.119.400117
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/33877350en_US
pubs.issue7en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume9en_US
dcterms.dateAccepted2019-05-02


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Attribution 3.0 United States
Except where otherwise noted, this item's license is described as Attribution 3.0 United States