Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/110353
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dc.creatorBarisic, M-
dc.creatorSousa, RS-
dc.creatorTripathy, SK-
dc.creatorMagiera, MM-
dc.creatorZaytsev, AV-
dc.creatorPereira, AL-
dc.creatorJanke, C-
dc.creatorGrishchuk, EL-
dc.creatorMaiato, H-
dc.date.accessioned2018-01-24T11:25:18Z-
dc.date.available2018-01-24T11:25:18Z-
dc.date.issued2015-
dc.identifier.issn0036-8075-
dc.identifier.urihttp://hdl.handle.net/10216/110353-
dc.description.abstractBefore chromosomes segregate into daughter cells, they align at the mitotic spindle equator, a process known as chromosome congression. Centromere-associated protein E (CENP-E)/Kinesin-7 is a microtubule plus-end-directed kinetochore motor required for congression of pole-proximal chromosomes. Because the plus-ends of many astral microtubules in the spindle point to the cell cortex, it remains unknown how CENP-E guides pole-proximal chromosomes specifically toward the equator. We found that congression of pole-proximal chromosomes depended on specific posttranslational detyrosination of spindle microtubules that point to the equator. In vitro reconstitution experiments demonstrated that CENP-E-dependent transport was strongly enhanced on detyrosinated microtubules. Blocking tubulin tyrosination in cells caused ubiquitous detyrosination of spindle microtubules, and CENP-E transported chromosomes away from spindle poles in random directions. Thus, CENP-E-driven chromosome congression is guided by microtubule detyrosination.-
dc.description.sponsorshipWe thank F. I. Ataullakhanov for help with the laser trap and data analysis; A. Kiyatkin, V. Mustyatsa, M. Molodtsov, A. Gautreau, G. Lakisic, and M. Barisic for technical assistance; and members of our laboratories for stimulating discussions. This work was supported by National Institutes of Health grant R01-GM098389 and RSG-14-018-01-CCG from the American Cancer Society to E.L.G.; by the Institut Curie, the Centre National de la Recherche Scientifique, the Institut National de la Sante et de la Recherche Medicale, the L'Agence Nationale de la Recherche (ANR) award ANR-12-BSV2-0007, INCA_6517, ANR-10-LBX-0038, part of the IDEX Idex PSL, ANR-10-IDEX-0001-02 PSL to C.J.; and Fundacao Luso-Americana para o Desenvolvimento (FLAD) Life Science 2020 and PRECISE grant from the European Research Council to H.M. A.V.Z. is supported by the RAS Presidium Grants "Mechanisms of the Molecular Systems Integration," " Molecular and Cell Biology programs," and Russian Fund for Basic Research Grant 12-04-00111-a and 13-00-40188. R.S.S. is supported by a fellowship from the Programa Graduado em Areas da Biologia Basica e Aplicada (GABBA) PhD program from the University of Porto. A.L.P. is supported by fellowship SFRH/BPD/66707/2009 from Fundacao para a Ciencia e a Tecnologia of Portugal. M.B., R.S.S., S.K.T., M.M.M., C.J., E.L.G., and H.M. designed the experiments; M.B. performed all experiments in cells; M. M. M. established and performed the tubulin purification protocol from HeLa cells; R.S.S. performed single-molecule experiments; S.K.T. performed force measurements; A.L.P. provided reagents; all authors analyzed data; H.M., E.L.G., and M.B. wrote the paper, with contributions from all authors; H.M. conceived and coordinated the project. Data described can be found in the main figures and supplementary materials. The authors declare no conflict of interests.-
dc.language.isoeng-
dc.publisherAmerican Association for the Advancement of Science-
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBPD%2F66707%2F2009/PT-
dc.relation.ispartofScience, vol. 348(6236), p. 799-803.-
dc.rightsopenAccess-
dc.subjectBridged Bicyclo Compounds Heterocyclic/pharmacology-
dc.subjectCell Line, Tumor-
dc.subjectChromosomal Proteins-
dc.subjectNon-Histone/antagonists & inhibitors-
dc.subjectChromosomal Proteins Non-Histone/genetics-
dc.subjectChromosomal Proteins Non-Histone/metabolism-
dc.subjectChromosome Segregation-
dc.subjectHumans-
dc.subjectMicrotubules/metabolism-
dc.subjectMitosis-
dc.subjectMolecular Imaging-
dc.subjectSarcosine/analogs & derivatives-
dc.subjectSarcosine/pharmacology-
dc.subjectSpindle Apparatus/metabolism-
dc.subjectTubulin/metabolism-
dc.subjectTyrosine/metabolism-
dc.titleMicrotubule detyrosination guides chromosomes during mitosis-
dc.typeArtigo em Revista Científica Internacional-
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde-
dc.identifier.doi10.1126/science.aaa5175-
dc.relation.publisherversionhttp://science.sciencemag.org/content/348/6236/799.long-
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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