MCAK associates with the tips of polymerizing microtubules
Open accessAbstract
MCAK is a member of the kinesin-13 family of microtubule (MT)-depolymerizing kinesins. We show that the potent MT depolymerizer MCAK tracks (treadmills) with the tips of polymerizing MTs in living cells. Tip tracking of MCAK is inhibited by phosphorylation and is dependent on the extreme COOH-terminal tail of MCAK. Tip tracking is not essential for MCAK's MT-depolymerizing activity. We propose that tip tracking is a mechanism by which MCAK is preferentially localized to regions of the cell that modulate the plus ends of MTs.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Overexpression of a dominant negative MCAK mutant led to a modest increase in chromosome missegregation in MDA-MB-231 cells.
“whereas overexpression of a dominant negative MCAK mutant12 (dnMCAK) led to a modest increase in chromosome missegregation in MDA-MB-231 cells.”
From Chromosomal instability drives metastasis through a cytosolic DNA response (2018) · cites this paper as [12]
MCAK plus-end tracking requires interaction between MCAK and members of the end-binding protein (EB) family.
“This plus-end tracking behavior requires the interaction between MCAK and members of the end-binding protein (EB) family [5-8]”
From In vitro reconstitution of the functional interplay between MCAK and EB3 at microtubule plus ends (2010) · cites this paper as [5]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Meijer, L., Nelson, D. J., Riazanski, V., Gabdoulkhakova, A. G., Héry-Arnaud, G., Berre, R. L., Loaëc, N., Oumata, N., Galons, H., Nowak, E., et al. (2016) · Journal of Innate Immunity · doi:10.1159/000444256 · Cited by 4,992 · see citing works
Meijer, L., Borgne, A., Mulner, O., Chong, J. P. J., Blow, J. J., Inagaki, N., Inagaki, M., Delcros, J., & Moulinoux, J. (1997) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1997.t01-2-00527.x · Cited by 1,352 · see citing works
A standardized kinesin nomenclature
Lawrence‐Dill, C. J., Dawe, R. K., Christie, K., Cleveland, D. W., Dawson, S. C., Endow, S. A., Goldstein, L. S. B., Goodson, H. V., Hirokawa, N., Howard, J., et al. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200408113 · Cited by 768 · see citing works
Self-citationKin I kinesins are microtubule-destabilizing enzymes
Desai, A., Verma, S., Mitchison, T. J., & Walczak, C. E. (1999) · Cell · doi:10.1016/s0092-8674(00)80960-5 · Cited by 708 · see citing works
Aurora B Regulates MCAK at the Mitotic Centromere
Andrews, P. D., Ovechkina, Y., MORRICE, N. A., Wagenbach, M., Duncan, K., Wordeman, L. G., & Swedlow, J. R. (2004) · Developmental Cell · doi:10.1016/s1534-5807(04)00025-5 · Cited by 531 · see citing works
Self-citationLan, W., Zhang, X., Kline-Smith, S. L., Rosasco, S. E., Barrett‐Wilt, G. A., Shabanowitz, J., Hunt, D. F., Walczak, C., & Stukenberg, P. T. (2004) · Current Biology · doi:10.1016/j.cub.2004.01.055 · Cited by 469 · see citing works
Hunter, A., Caplow, M., Coy, D. L., Hancock, W., Diez, S., Wordeman, L., & Howard, J. (2003) · Molecules and Cells · doi:10.1016/s1097-2765(03)00049-2 · Cited by 404 · see citing works
Self-citationTournebize, R., Popov, A. V., Kinoshita, K., Ashford, A. J., Rybina, S., Pozniakovsky, A., Mayer, T. U., Walczak, C., Karsenti, E., & Hyman, A. A. (1999) · Nature Cell Biology · doi:10.1038/71330 · Cited by 326 · see citing works
Two mitotic kinesins cooperate to drive sister chromatid separation during anaphase
Rogers, G. C., Rogers, S. L., Schwimmer, T. A., Ems-McClung, S. C., Walczak, C., Vale, R. D., Scholey, J. M., & Sharp, D. J. (2003) · Nature · doi:10.1038/nature02256 · Cited by 317 · see citing works
Mitotic Centromere–associated Kinesin Is Important for Anaphase Chromosome Segregation
Maney, T., Hunter, A. W., Wagenbach, M., & Wordeman, L. G. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.142.3.787 · Cited by 289 · see citing works
Self-citationOncoprotein 18 is a phosphorylation‐responsive regulator of microtubule dynamics.
Marklund, U., Larsson, N., Gradin, H. M., Brattsand, G., & Gullberg, M. H. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00914.x · Cited by 279 · see citing works
Ganem, N. J., & Compton, D. A. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200404012 · Cited by 227 · see citing works
Carvalho, P., Tirnauer, J. S., & Pellman, D. S. (2003) · Trends in Cell Biology · doi:10.1016/s0962-8924(03)00074-6 · Cited by 221 · see citing works
Ohi, R., Sapra, K. T., Howard, J., & Mitchison, T. J. (2004) · Molecular Biology of the Cell · doi:10.1091/mbc.e04-02-0082 · Cited by 220 · see citing works
Ogawa, T., Nitta, R., Okada, Y., & Hirokawa, N. (2004) · Cell · doi:10.1016/s0092-8674(04)00129-1 · Cited by 199 · see citing works
Gaetz, J., & Kapoor, T. M. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200404015 · Cited by 197 · see citing works
The TOGp protein is a new human microtubule-associated protein homologous to the Xenopus XMAP215
Charrasse, S., Schroeder, M., Gauthier‐Rouvière, C., Ango, F., Cassimeris, L., Gard, D. L., & Larroque, C. (1998) · Journal of Cell Science · doi:10.1242/jcs.111.10.1371 · Cited by 175 · see citing works
Mennella, V., Rogers, G. C., Rogers, S. L., Buster, D. W., Vale, R. D., & Sharp, D. J. (2005) · Nature Cell Biology · doi:10.1038/ncb1222 · Cited by 154 · see citing works
A Mechanism for Microtubule Depolymerization by KinI Kinesins
Moores, C. A., Yu, M., Guo, J., Béraud, C., Sakowicz, R., & Milligan, R. A. (2002) · Molecular Cell · doi:10.1016/s1097-2765(02)00503-8 · Cited by 146 · see citing works
The mechanism, function and regulation of depolymerizing kinesins during mitosis
Moore, A. T., & Wordeman, L. G. (2004) · Trends in Cell Biology · doi:10.1016/j.tcb.2004.09.001 · Cited by 107 · see citing works
Self-citationK-loop insertion restores microtubule depolymerizing activity of a “neckless” MCAK mutant
Ovechkina, Y., Wagenbach, M., & Wordeman, L. G. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200205089 · Cited by 102 · see citing works
Self-citationThe offloading model for dynein function
Lee, W., Kaiser, M. A., & Cooper, J. A. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200407036 · Cited by 97 · see citing works
Newton, C. N., Wagenbach, M., Ovechkina, Y., Wordeman, L. G., & Wilson, L. (2004) · FEBS Letters · doi:10.1016/j.febslet.2004.06.093 · Cited by 48 · see citing works
Self-citationMoore, A. T., & Wordeman, L. G. (2004) · Biochemical Journal · doi:10.1042/bj20040736 · Cited by 39 · see citing works
Self-citationDynamic properties of APC‐decorated microtubules in living cells
Dayanandan, R., Butler, R., Gordon‐Weeks, P. R., Matus, A. I., Kaech, S., Lovestone, S., Anderton, B. H., & Gallo, J. (2003) · Cell Motility and the Cytoskeleton · doi:10.1002/cm.10096 · Cited by 9 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Chromosomal instability drives metastasis through a cytosolic DNA response
Bakhoum, S. F., Ngo, B., Laughney, A. M., Cavallo, J.-A., Murphy, C. J., Ly, P., Shah, P., Sriram, R. K., Watkins, T. B. K., Taunk, N. K., et al. (2018) · Nature · doi:10.1038/nature25432 · Cited by 1,638 · see citing works
Tracking the ends: a dynamic protein network controls the fate of microtubule tips
Akhmanova, A., & Steinmetz, M. O. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2369 · Cited by 1,047 · see citing works
Rath, O., & Kozielski, F. (2012) · Nature reviews. Cancer · doi:10.1038/nrc3310 · Cited by 497 · see citing works
Motor-dependent microtubule disassembly driven by tubulin tyrosination
Peris, L., Wagenbach, M., Lafanéchère, L., Brocard, J., Moore, A. T., Kozielski, F., Job, D., Wordeman, L. G., & Andrieux, A. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200902142 · Cited by 370 · see citing works
Self-citationPowering membrane traffic in endocytosis and recycling
Soldati, T., & Schliwa, M. (2006) · Nature reviews. Molecular cell biology · doi:10.1038/nrm2060 · Cited by 378 · see citing works
Peris, L., Théry, M., Fauré, J., Saoudi, Y., Lafanéchère, L., Chilton, J. K., Gordon‐Weeks, P. R., Galjart, N., Bornens, M., Wordeman, L. G., et al. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200512058 · Cited by 347 · see citing works
Self-citationThe Kinesin-8 Motor Kif18A Suppresses Kinetochore Movements to Control Mitotic Chromosome Alignment
Stumpff, J. K., von Dassow, G., Wagenbach, M., Asbury, C. L., & Wordeman, L. G. (2008) · Developmental Cell · doi:10.1016/j.devcel.2007.11.014 · Cited by 332 · see citing works
Self-citationGupta, M. L., Carvalho, P., Roof, D. M., & Pellman, D. S. (2006) · Nature Cell Biology · doi:10.1038/ncb1457 · Cited by 322 · see citing works
Non-cell-autonomous cancer progression from chromosomal instability
Li, J., Hubisz, M. J., Earlie, E. M., Paez, M. A. D., Hong, C., Varela, A., Lettera, E., Deyell, M., Tavora, B., Havel, J. J., et al. (2023) · Nature · doi:10.1038/s41586-023-06464-z · Cited by 321 · see citing works
Microtubule polymerases and depolymerases
Howard, J., & Hyman, A. A. (2007) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2006.12.009 · Cited by 294 · see citing works
Inactivation of a Human Kinetochore by Specific Targeting of Chromatin Modifiers
Nakano, M., Cardinale, S., Noskov, V., Gassmann, R., Vagnarelli, P., Kandels-Lewis, S., Larionov, V., Earnshaw, W., & Masumoto, H. (2008) · Developmental Cell · doi:10.1016/j.devcel.2008.02.001 · Cited by 267 · see citing works
Manning, A. L., Ganem, N. J., Bakhoum, S. F. W., Wagenbach, M., Wordeman, L. G., & Compton, D. A. (2007) · Molecular Biology of the Cell · doi:10.1091/mbc.e07-02-0110 · Cited by 243 · see citing works
Self-citationPlus-End-Tracking Proteins and Their Interactions at Microtubule Ends
Galjart, N. (2010) · Current Biology · doi:10.1016/j.cub.2010.05.022 · Cited by 223 · see citing works
How kinesin motor proteins drive mitotic spindle function: Lessons from molecular assays
Wordeman, L. G. (2010) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2010.01.018 · Cited by 192 · see citing works
Self-citationRegulation of microtubule dynamic instability
van der Vaart, B., Akhmanova, A. S., & Straube, A. (2009) · Biochemical Society Transactions · doi:10.1042/bst0371007 · Cited by 165 · see citing works
Microtubule-Depolymerizing Kinesins
Walczak, C., Gayek, S., & Ohi, R. (2013) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-101512-122345 · Cited by 165 · see citing works
In vitro reconstitution of the functional interplay between MCAK and EB3 at microtubule plus ends
Montenegro Gouveia, S., Leslie, K., Kapitein, L. C., Buey, R. M., Grigoriev, I., Wagenbach, M., Smal, I., Meijering, E., Hoogenraad, C. C., Wordeman, L., et al. (2010) · Current Biology · doi:10.1016/j.cub.2010.08.020 · Cited by 147 · see citing works
Self-citationKinesin-13s in mitosis: Key players in the spatial and temporal organization of spindle microtubules
Ems-McClung, S. C., & Walczak, C. E. (2010) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2010.01.016 · Cited by 154 · see citing works
Oncogenic role of kinesin proteins and targeting kinesin therapy
Liu, X., Gong, H., & Huang, K. (2013) · Cancer Science · doi:10.1111/cas.12138 · Cited by 149 · see citing works
Tanenbaum, M. E., Macurek, L., van der Vaart, B., Galli, M., Akhmanova, A., & Medema, R. H. (2011) · Current Biology · doi:10.1016/j.cub.2011.07.017 · Cited by 148 · see citing works
+TIPs: SxIPping along microtubule ends
Kumar, P., & Wittmann, T. (2012) · Trends in Cell Biology · doi:10.1016/j.tcb.2012.05.005 · Cited by 146 · see citing works
Kinesin-13 Regulates Flagellar, Interphase, and Mitotic Microtubule Dynamics in Giardia intestinalis
Dawson, S. C., Sagolla, M. S., Mancuso, J. J., Woessner, D. J., House, S. A., Fritz‐Laylin, L. K., & Cande, W. Z. (2007) · Eukaryotic Cell · doi:10.1128/ec.00128-07 · Cited by 146 · see citing works
Kinesin-5 Regulation and Function in Mitosis
Mann, B. J., & Wadsworth, P. (2018) · Trends in Cell Biology · doi:10.1016/j.tcb.2018.08.004 · Cited by 144 · see citing works
MCAK facilitates chromosome movement by promoting kinetochore microtubule turnover
Wordeman, L. G., Wagenbach, M., & von Dassow, G. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200707120 · Cited by 138 · see citing works
Self-citationLateral to End-on Conversion of Chromosome-Microtubule Attachment Requires Kinesins CENP-E and MCAK
Shrestha, R. L., & Draviam, V. M. (2013) · Current Biology · doi:10.1016/j.cub.2013.06.040 · Cited by 137 · see citing works
Zhang, X., Lan, W., Ems-McClung, S. C., Stukenberg, P. T., & Walczak, C. (2007) · Molecular Biology of the Cell · doi:10.1091/mbc.e07-01-0086 · Cited by 126 · see citing works
Aurora A phosphorylates MCAK to control ran-dependent spindle bipolarity
Zhang, X., Ems-McClung, S. C., & Walczak, C. E. (2008) · Molecular Biology of the Cell · doi:10.1091/mbc.e08-02-0198 · Cited by 123 · see citing works
Shi, W., Dai, M., Zhang, C., Teng, K., Wang, F., Li, H., Sun, W., Feng, Z., Kang, T., Guan, X., et al. (2020) · Protein & Cell · doi:10.1007/s13238-020-00766-y · Cited by 121 · see citing works
Circular RNA ZNF609/CKAP5 mRNA interaction regulates microtubule dynamics and tumorigenicity
Rossi, F., Beltran-Nebot, M., Damizia, M., Grelloni, C., Colantoni, A., Setti, A., Timoteo, G. D., Dattilo, D., Centrón-Broco, A., Nicoletti, C., et al. (2021) · Molecular Cell · doi:10.1016/j.molcel.2021.11.032 · Cited by 104 · see citing works
Paxillin-dependent stimulation of microtubule catastrophes at focal adhesion sites
Efimov, A., Schiefermeier-Mach, N., Grigoriev, I., Brown, M. C., Turner, C. E., Small, J. V., & Kaverina, I. (2008) · Journal of Cell Science · doi:10.1242/jcs.012666 · Cited by 100 · see citing works
Motor proteins at the microtubule plus-end
Wu, X., Xiang, X., & Hammer, J. A. (2006) · Trends in Cell Biology · doi:10.1016/j.tcb.2006.01.004 · Cited by 97 · see citing works
Lucky 13-microtubule depolymerisation by kinesin-13 motors
Moores, C. A., & Milligan, R. A. (2006) · Journal of Cell Science · doi:10.1242/jcs.03224 · Cited by 92 · see citing works
Action and interactions at microtubule ends
Morrison, E. E. (2007) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-007-6360-3 · Cited by 90 · see citing works
PLK1 Phosphorylates Mitotic Centromere-associated Kinesin and Promotes Its Depolymerase Activity
Zhang, L., Shao, H., Huang, Y., Yan, F., Chu, Y., Hou, H. T., Zhu, M., Fu, C., Aikhionbare, F. O., Fang, G., et al. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.165340 · Cited by 87 · see citing works
Gierke, S., & Wittmann, T. (2012) · Current Biology · doi:10.1016/j.cub.2012.02.069 · Cited by 87 · see citing works
Long astral microtubules uncouple mitotic spindles from the cytokinetic furrow
Rankin, K. E., & Wordeman, L. G. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.201004017 · Cited by 87 · see citing works
Self-citationTIP150 interacts with and targets MCAK at the microtubule plus ends
Jiang, K., Wang, J., Liu, J. L., Ward, T. L., Wordeman, L. G., Davidson, A. J., Wang, F., & Yao, X. (2009) · EMBO Reports · doi:10.1038/embor.2009.94 · Cited by 81 · see citing works
Self-citationEms-McClung, S. C., Hainline, S. G., Devare, J., Zong, H., Cai, S., Carnes, S. K., Shaw, S. L., & Walczak, C. E. (2013) · Current Biology · doi:10.1016/j.cub.2013.10.054 · Cited by 73 · see citing works
Nonredundant Functions of Kinesin-13s during Meiotic Spindle Assembly
Ohi, R., Burbank, K. S., Liu, Q., & Mitchison, T. J. (2007) · Current Biology · doi:10.1016/j.cub.2007.04.057 · Cited by 79 · see citing works
Domnitz, S. B., Wagenbach, M., Decarreau, J. A., & Wordeman, L. G. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201108147 · Cited by 78 · see citing works
Self-citationKumar, P., Chimenti, M. S., Pemble, H., Schönichen, A., Thompson, O., Jacobson, M. P., & Wittmann, T. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.316661 · Cited by 74 · see citing works
Hertzer, K. M., Ems-McClung, S. C., Kline-Smith, S. L., Lipkin, T. G., Gilbert, S. P., & Walczak, C. (2005) · Molecular Biology of the Cell · doi:10.1091/mbc.e05-08-0821 · Cited by 70 · see citing works
Mitotic centromere-associated kinesin (MCAK): a potential cancer drug target
Sanhaji, M., Friel, C. T., Wordeman, L. G., Louwen, F., & Yuan, J. (2011) · Oncotarget · doi:10.18632/oncotarget.416 · Cited by 70 · see citing works
Self-citationMolecular basis of vasohibins-mediated detyrosination and its impact on spindle function and mitosis
Liao, S., Rajendraprasad, G., Wang, N., Eibes, S., Gao, J., Yu, H., Wu, G., Tu, X., Huang, H., Barišić, M., et al. (2019) · Cell Research · doi:10.1038/s41422-019-0187-y · Cited by 70 · see citing works
Lee, T., Langford, K. J., Askham, J. M., Brüning-Richardson, A., & Morrison, E. E. (2008) · Oncogene · doi:10.1038/sj.onc.1210867 · Cited by 69 · see citing works
Cell and Molecular Biology of Microtubule Plus End Tracking Proteins
Gouveia, S. M., & Akhmanova, A. S. (2010) · International review of cytology · doi:10.1016/b978-0-12-381047-2.00001-3 · Cited by 66 · see citing works
ATR promotes clearance of damaged DNA and damaged cells by rupturing micronuclei
Joo, Y. K., Black, E. M., Trier, I., Haakma, W. E., Zou, L., & Kabeche, L. (2023) · Molecular Cell · doi:10.1016/j.molcel.2023.09.003 · Cited by 67 · see citing works
Ferreira, J. G. G., Pereira, A. J., Akhmanova, A. S., & Maiato, H. (2013) · The Journal of Cell Biology · doi:10.1083/jcb.201301131 · Cited by 63 · see citing works
Tamura, N., & Draviam, V. M. (2012) · Open Biology · doi:10.1098/rsob.120132 · Cited by 59 · see citing works
Cilia Distal Domain: Diversity in Evolutionarily Conserved Structures
Soares, H., Carmona, B., Nolasco, S., Melo, L. V., & Gonçalves, J. (2019) · Cells · doi:10.3390/cells8020160 · Cited by 59 · see citing works
Rac1 and Aurora A regulate MCAK to polarize microtubule growth in migrating endothelial cells
Braun, A., Dang, K., Buslig, F., Baird, M. A., Davidson, M. W., Waterman, C. M., & Myers, K. A. (2014) · The Journal of Cell Biology · doi:10.1083/jcb.201401063 · Cited by 58 · see citing works
A new role for kinesin-directed transport of Bik1p (CLIP-170) in Saccharomyces cerevisiae
Caudron, F., Andrieux, A., Job, D., & Boscheron, C. (2008) · Journal of Cell Science · doi:10.1242/jcs.023374 · Cited by 56 · see citing works
Self-citationIntrinsic and Extrinsic Factors Affecting Microtubule Dynamics in Normal and Cancer Cells
Borys, F., Joachimiak, E., Krawczyk, H., & Fabczak, H. (2020) · Molecules · doi:10.3390/molecules25163705 · Cited by 55 · see citing works
Molecular insight into the regulation and function of MCAK
Ritter, A., Kreis, N., Louwen, F., Wordeman, L. G., & Yuan, J. (2016) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409238.2016.1178705 · Cited by 54 · see citing works
Self-citationEB1 promotes microtubule dynamics by recruiting Sentin in Drosophila cells
Li, W., Miki, T., Watanabe, T., Kakeno, M., Sugiyama, I., Kaibuchi, K., & Goshima, G. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201101108 · Cited by 53 · see citing works
Move in for the kill: motile microtubule regulators
Su, X., Ohi, R., & Pellman, D. S. (2012) · Trends in Cell Biology · doi:10.1016/j.tcb.2012.08.003 · Cited by 53 · see citing works
TTBK2 with EB1/3 regulates microtubule dynamics in migrating cells through KIF2A phosphorylation
Watanabe, T., Kakeno, M., Matsui, T., Sugiyama, I., Arimura, N., Matsuzawa, K., Shirahige, A., Ishidate, F., Nishioka, T., Taya, S., et al. (2015) · The Journal of Cell Biology · doi:10.1083/jcb.201412075 · Cited by 53 · see citing works
Ems-McClung, S. C., Hertzer, K. M., Zhang, X., Miller, M. W., & Walczak, C. (2006) · Molecular Biology of the Cell · doi:10.1091/mbc.e06-08-0724 · Cited by 47 · see citing works
Chu, L., Zhu, T., Liu, X., Yu, R., Bacanamwo, M., Dou, Z., Chu, Y., Zou, H., Gibbons, G. H., Wang, D., et al. (2012) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjs023 · Cited by 47 · see citing works
Deciphering protein function during mitosis in PtK cells using RNAi
Stout, J. R., Rizk, R. S., Kline-Smith, S. L., & Walczak, C. (2006) · BMC Cell Biology · doi:10.1186/1471-2121-7-26 · Cited by 47 · see citing works
Noda, Y., Niwa, S., Homma, N., Fukuda, H., Imajo‐Ohmi, S., & Hirokawa, N. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1107808109 · Cited by 45 · see citing works
Aurora A, MCAK, and Kif18b promote Eg5-independent spindle formation
van Heesbeen, R. G. H. P., Raaijmakers, J. A., Tanenbaum, M. E., Halim, V. A., Lelieveld, D., Lieftink, C., Heck, A. J. R., Egan, D. A., & Medema, R. H. (2016) · Chromosoma · doi:10.1007/s00412-016-0607-4 · Cited by 43 · see citing works
Examination of actin and microtubule dependent APC localisations in living mammalian cells
Langford, K. J., Askham, J. M., Lee, T., Adams, M., & Morrison, E. E. (2006) · BMC Cell Biology · doi:10.1186/1471-2121-7-3 · Cited by 44 · see citing works
The molecular basis for kinesin functional specificity during mitosis
Welburn, J. P. I. (2013) · Cytoskeleton · doi:10.1002/cm.21135 · Cited by 41 · see citing works
Regulation of localization and activity of the microtubule depolymerase MCAK
Tanenbaum, M. E., Medema, R. H., & Akhmanova, A. S. (2011) · BioArchitecture · doi:10.4161/bioa.1.2.15807 · Cited by 40 · see citing works
A unique kinesin-8 surface loop provides specificity for chromosome alignment
Kim, H., Fonseca, C. L., & Stumpff, J. K. (2014) · Molecular Biology of the Cell · doi:10.1091/mbc.e14-06-1132 · Cited by 40 · see citing works
Polo-like kinase 1 regulates the stability of the mitotic centromere-associated kinesin in mitosis
Sanhaji, M., Ritter, A., Belsham, H. R., Friel, C. T., Roth, S., Louwen, F., & Yuan, J. (2014) · Oncotarget · doi:10.18632/oncotarget.1861 · Cited by 39 · see citing works
Talapatra, S. K., Harker, B., & Welburn, J. P. I. (2015) · eLife · doi:10.7554/elife.06421 · Cited by 39 · see citing works
Wickstead, B., Carrington, J. T., Gluenz, E., & Keith Gull, B. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015020 · Cited by 39 · see citing works
Qu, Y., Hahn, I., Lees, M., Parkin, J., Voelzmann, A., Dorey, K., Rathbone, A., Friel, C. T., Allan, V., Okenve-Ramos, P., et al. (2019) · eLife · doi:10.7554/elife.50319 · Cited by 38 · see citing works
Ritter, A., Sanhaji, M., Friemel, A., Roth, S., Rolle, U., Louwen, F., & Yuan, J. (2015) · Cell Cycle · doi:10.1080/15384101.2015.1068481 · Cited by 38 · see citing works
Kinesins and protein kinases: Key players in the regulation of microtubule dynamics and organization
Daire, V., & Poüs, C. (2011) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2011.02.012 · Cited by 37 · see citing works
McHugh, T., Zou, J., Volkov, V. A., Bertin, A., Talapatra, S. K., Rappsilber, J., Dogterom, M., & Welburn, J. P. I. (2018) · Journal of Cell Science · doi:10.1242/jcs.228353 · Cited by 36 · see citing works
Vogt, E.-J., Sanhaji, M., Klein, W., Seidel, T., Wordeman, L. G., & Eichenlaub-Ritter, U. (2010) · Molecular Human Reproduction · doi:10.1093/molehr/gaq025 · Cited by 36 · see citing works
Self-citationA kinesin-mediated mechanism that couples centrosomes to nuclei
Tikhonenko, I., Magidson, V., Gräf, R., Khodjakov, A. L., & Koonce, M. P. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-1205-0 · Cited by 35 · see citing works
Cao, D., Su, Z., Wang, W., Wu, H., Liu, X., Akram, S., Qin, B., Zhou, J., Zhuang, X., Adams, G., et al. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.673517 · Cited by 34 · see citing works
Zheng, R., Du, Y.-L., Wang, X., Liao, T., Zhang, Z., Wang, N., Li, X., Shen, Y., Shi, L., Luo, J., et al. (2022) · eLife · doi:10.7554/elife.72483 · Cited by 33 · see citing works
Clathrin’s adaptor interaction sites are repurposed to stabilize microtubules during mitosis
Rondelet, A., Lin, Y., Singh, D., Porfetye, A. T., Thakur, H. C., Hecker, A., Brinkert, P., Schmidt, N., Bendre, S., Müller, F., et al. (2020) · The Journal of Cell Biology · doi:10.1083/jcb.201907083 · Cited by 31 · see citing works
Spatial regulation of astral microtubule dynamics by Kif18B in PtK cells
Walczak, C., Zong, H., Jain, S., & Stout, J. R. (2016) · Molecular Biology of the Cell · doi:10.1091/mbc.e16-04-0254 · Cited by 31 · see citing works
Parts list for a microtubule depolymerising kinesin
Friel, C. T., & Welburn, J. P. I. (2018) · Biochemical Society Transactions · doi:10.1042/bst20180350 · Cited by 31 · see citing works
A Perikinetochoric Ring Defined by MCAK and Aurora-B as a Novel Centromere Domain
Parra, M. T., Gómez, R., Viera, A., Page, J., Calvente, A., Wordeman, L. G., Rufas, J. S., & Suja, J. A. (2006) · PLoS Genetics · doi:10.1371/journal.pgen.0020084 · Cited by 31 · see citing works
Self-citationSyred, H. M., Welburn, J., Rappsilber, J., & Ohkura, H. (2013) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m113.028563 · Cited by 25 · see citing works
Microtubule Plus-End Tracking Proteins and Their Roles in Cell Division
Ferreira, J. G. G., Pereira, A. L., & Maiato, H. (2014) · International review of cytology · doi:10.1016/b978-0-12-800255-1.00002-8 · Cited by 30 · see citing works
Singh, D., Schmidt, N., Müller, F., Bange, T., & Bird, A. W. (2020) · Current Biology · doi:10.1016/j.cub.2020.11.040 · Cited by 30 · see citing works
Motor domain phosphorylation and regulation of the Drosophila kinesin 13, KLP10A
Mennella, V., Tan, D., Buster, D. W., Asenjo, A. B., Rath, U., Ma, A., Sosa, H., & Sharp, D. J. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200902113 · Cited by 30 · see citing works
Zaganjor, E., Osborne, J. K., Weil, L. M., Díaz-Martínez, L. A., Gonzales, J. X., Singel, S. M., Larsen, J. E., Girard, L., Minna, J. D., & Cobb, M. H. (2013) · Oncogene · doi:10.1038/onc.2013.486 · Cited by 29 · see citing works
Kim, J. (2021) · World Journal of Surgical Oncology · doi:10.1186/s12957-021-02301-7 · Cited by 28 · see citing works
Zhang, L., Shao, H., Zhu, T., Xia, P., Wang, Z., Liu, L., Yan, M., Hill, D. L., Fang, G., Chen, Z., et al. (2013) · Scientific Reports · doi:10.1038/srep01681 · Cited by 27 · see citing works
Length control of microtubules by depolymerizing motor proteins
Govindan, B. S., Gopalakrishnan, M., & Chowdhury, D. (2008) · Europhysics Letters (EPL) · doi:10.1209/0295-5075/83/40006 · Cited by 27 · see citing works
Potent microtubule-depolymerizing activity of a mitotic Kif18b–MCAK–EB network
McHugh, T., & Welburn, J. P. I. (2022) · Journal of Cell Science · doi:10.1242/jcs.260144 · Cited by 25 · see citing works
Probing microtubule polymerisation state at single kinetochores during metaphase chromosome motion
Armond, J. W., Vladimirou, E., Erent, M., McAinsh, A. D., & Burroughs, N. J. (2015) · Journal of Cell Science · doi:10.1242/jcs.168682 · Cited by 25 · see citing works
Corrigan, A. M., Shrestha, R. L., Zulkipli, I. N., Hiroi, N. F., Liu, Y., Tamura, N., Yang, B., Patel, J., Funahashi, A., Donald, A. M., et al. (2013) · Cell Cycle · doi:10.4161/cc.25671 · Cited by 24 · see citing works
Global and local control of microtubule destabilization promoted by a catastrophe kinesin MCAK/XKCM1
Kinoshita, K., Noetzel, T. L., Arnal, I., Drechsel, D. N., & Hyman, A. A. (2006) · Journal of Muscle Research and Cell Motility · doi:10.1007/s10974-005-9045-2 · Cited by 24 · see citing works
Significance of microtubule catastrophes at focal adhesion sites
Efimov, A., & Kaverina, I. (2009) · Cell Adhesion & Migration · doi:10.4161/cam.3.3.8858 · Cited by 22 · see citing works
Divergent microtubule assembly rates after short- versus long-term loss of end-modulating kinesins
Wordeman, L. G., Decarreau, J. A., Vicente, J. J., & Wagenbach, M. (2016) · Molecular Biology of the Cell · doi:10.1091/mbc.e15-11-0803 · Cited by 22 · see citing works
Self-citationKreis, N., Moon, H. H., Wordeman, L. G., Louwen, F., Solbach, C., Yuan, J., & Ritter, A. (2024) · Critical Reviews in Clinical Laboratory Sciences · doi:10.1080/10408363.2024.2309933 · Cited by 21 · see citing works
Self-citationThe activity regulation of the mitotic centromere-associated kinesin by Polo-like kinase 1
Ritter, A., Sanhaji, M., Steinhäuser, K., Roth, S., Louwen, F., & Yuan, J. (2014) · Oncotarget · doi:10.18632/oncotarget.2843 · Cited by 19 · see citing works
Hu, Z., Liang, Y., Meng, D., Wang, L., & Pan, J. (2015) · International review of cytology · doi:10.1016/bs.ircmb.2015.01.008 · Cited by 19 · see citing works
Ross, P. J., Perez, G. I., Ko, T., Yoo, M. S., & Cibelli, J. B. (2006) · BioTechniques · doi:10.2144/000112310 · Cited by 18 · see citing works
Guan, C., Hua, S., & Jiang, K. (2023) · The EMBO Journal · doi:10.15252/embj.2022112953 · Cited by 15 · see citing works
- Authors
- Moore, A. T., Rankin, K. E., von Dassow, G., Peris, L., Wagenbach, M., Ovechkina, Y., Andrieux, A., Job, D., & Wordeman, L.
- Affiliations
- University of Washington (US)
- 2Center for Cell Dynamics, Friday Harbor Labs, University of Washington, Friday Harbor, WA 98250
- Inserm (FR)
- Corresponding author
- Wordeman, Linda
- Venue
- The Journal of Cell Biology
- Publisher
- Rockefeller University Press
- Published
- 2005-05-09
- Volume
- 169
- Issue
- 3
- Pages
- 391-397
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- PMC
- PMC2171944
- OpenAlex
- W2151206507
- Cited by
- 141
- References
- 25
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 5 · 2023: 6 · 2022: 3 · 2021: 3 · 2020: 6 · 2019: 4 · 2018: 7 · 2017: 2 · 2016: 11 · 2015: 8 · 2014: 7 · 2013: 10 · 2012: 12
- FWCI
- 4.20
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- cc-by-nc-sa
- Locations
- The Journal of Cell Biology (publishedVersion)
- PubMed Central (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- HAL (submittedVersion, other-oa)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- National Institute of General Medical Sciences (GM-07270, F31GM065061, T32GM007270, P50GM066050, R01GM069429, GM69429, GM65061, GM066050)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Health Sciences › Medicine › Oncology › Cancer Treatment and Pharmacology
- Physical Sciences › Chemistry › Organic Chemistry › Synthesis and biological activity
- Keywords
- MCAK, kinesin-13, microtubule depolymerization, microtubule plus ends, microtubule assembly, phosphorylation, protein localization, microtubule dynamics
- MeSH terms
- Animals, Cell Compartmentation, Cricetinae, HeLa Cells, Humans, Microtubules, Phosphorylation, Polymers, Recombinant Fusion Proteins, CHO Cells, Kinesins, Cell Polarity, Protein Structure, Tertiary, Microscopy, Video, Protein Transport, Green Fluorescent Proteins
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review