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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003524naa a2200613 4500
001oai:gup.ub.gu.se/293525
003SwePub
008240528s2020 | |||||||||||000 ||eng|
024a https://gup.ub.gu.se/publication/2935252 URI
024a https://doi.org/10.1083/jcb.2019070832 DOI
040 a (SwePub)gu
041 a eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Rondelet, A.4 aut
2451 0a Clathrin's adaptor interaction sites are repurposed to stabilize microtubules during mitosis
264 c 2020-01-13
264 1b Rockefeller University Press,c 2020
520 a Clathrin ensures mitotic spindle stability and efficient chromosome alignment, independently of its vesicle trafficking function. Although clathrin localizes to the mitotic spindle and kinetochore fiber microtubule bundles, the mechanisms by which clathrin stabilizes microtubules are unclear. We show that clathrin adaptor interaction sites on clathrin heavy chain (CHC) are repurposed during mitosis to directly recruit the microtubule-stabilizing protein GTSE1 to the spindle. Structural analyses reveal that these sites interact directly with clathrin-box motifs on GTSE1. Disruption of this interaction releases GTSE1 from spindles, causing defects in chromosome alignment. Surprisingly, this disruption destabilizes astral microtubules, but not kinetochore-microtubule attachments, and chromosome alignment defects are due to a failure of chromosome congression independent of kinetochore-microtubule attachment stability. GTSE1 recruited to the spindle by clathrin stabilizes microtubules by inhibiting the microtubule depolymerase MCAK. This work uncovers a novel role of clathrin adaptor-type interactions to stabilize nonkinetochore fiber microtubules to support chromosome congression, defining for the first time a repurposing of this endocytic interaction mechanism during mitosis.
650 7a NATURVETENSKAPx Biologix Biokemi och molekylärbiologi0 (SwePub)106022 hsv//swe
650 7a NATURAL SCIENCESx Biological Sciencesx Biochemistry and Molecular Biology0 (SwePub)106022 hsv//eng
653 a n-terminal domain
653 a centromere-associated kinesin
653 a chromosome
653 a congression
653 a bac transgeneomics
653 a kinetochore fibers
653 a multiple sites
653 a xenopus eggs
653 a d-tacc
653 a protein
653 a dynamics
653 a Cell Biology
700a Lin, Y. C.4 aut
700a Singh, D.4 aut
700a Porfetye, A. T.4 aut
700a Thakurle, H. C.4 aut
700a Hecker, A.4 aut
700a Brinket, P.4 aut
700a Schmidt, N.4 aut
700a Bendre, S.4 aut
700a Muller, F.4 aut
700a Mazul, L.4 aut
700a Widlund, Per Ou Gothenburg University,Göteborgs universitet,Institutionen för biomedicin,Institute of Biomedicine4 aut0 (Swepub:gu)xwidlp
700a Bange, T.4 aut
700a Hiller, M.4 aut
700a Vetter, I. R.4 aut
700a Bird, A. W.4 aut
710a Göteborgs universitetb Institutionen för biomedicin4 org
773t Journal of Cell Biologyd : Rockefeller University Pressg 219:2q 219:2x 0021-9525x 1540-8140
856u https://rupress.org/jcb/article-pdf/219/2/e201907083/1398027/jcb_201907083.pdf
8564 8u https://gup.ub.gu.se/publication/293525
8564 8u https://doi.org/10.1083/jcb.201907083

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