Functionally distinct kinesin-13 family members cooperate to regulate microtubule dynamics during interphase
Abstract
Regulation of microtubule polymerization and depolymerization is required for proper cell development. Here, we report that two proteins of the Drosophila melanogaster kinesin-13 family, KLP10A and KLP59C, cooperate to drive microtubule depolymerization in interphase cells. Analyses of microtubule dynamics in S2 cells depleted of these proteins indicate that both proteins stimulate depolymerization, but alter distinct parameters of dynamic instability; KLP10A stimulates catastrophe (a switch from growth to shrinkage) whereas KLP59C suppresses rescue (a switch from shrinkage to growth). Moreover, immunofluorescence and live analyses of cells expressing tagged kinesins reveal that KLP10A and KLP59C target to polymerizing and depolymerizing microtubule plus ends, respectively. Our data also suggest that KLP10A is deposited on microtubules by the plus-end tracking protein, EB1. Our findings support a model in which these two members of the kinesin-13 family divide the labour of microtubule depolymerization.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
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?
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 [8]
Cites
Dynamic instability of microtubule growth
Mitchison, T., & Kirschner, M. (1984) · Nature · doi:10.1038/312237a0 · Cited by 3,337 · see citing works
Clemens, J. C., Worby, C. A., Simonson-Leff, N., Muda, M., Maehama, T., Hemmings, B. A., & Dixon, J. E. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.110149597 · Cited by 843 · 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-citationDynamics and mechanics of the microtubule plus end
Howard, J., & Hyman, A. A. (2003) · Nature · doi:10.1038/nature01600 · Cited by 750 · see citing works
Kin 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
All kinesin superfamily protein, KIF, genes in mouse and human
Miki, H., Setou, M., Kaneshiro, K., & Hirokawa, N. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.111145398 · Cited by 703 · see citing works
Walczak, C., Mitchison, T. J., & Desai, A. B. (1996) · Cell · doi:10.1016/s0092-8674(00)80991-5 · Cited by 534 · 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
The design plan of kinesin motors
Vale, R. D., & Fletterick, R. J. (1997) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.13.1.745 · Cited by 474 · 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
APC binds to the novel protein EB1.
Su, L.-K., Burrell, M., HILL, D. E., Gyuris, J., Brent, R., Wiltshire, R. N., Trent, J. M., Vogelstein, B., & Kinzler, K. W. (1995) · PubMed · Cited by 445 · see citing works
Belmont, L. D., Hyman, A. A., Sawin, K. E., & Mitchison, T. J. (1990) · Cell · doi:10.1016/0092-8674(90)90022-7 · Cited by 443 · see citing works
Drosophila EB1 is important for proper assembly, dynamics, and positioning of the mitotic spindle
Rogers, S. L., Rogers, G. C., Sharp, D. J., & Vale, R. D. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200202032 · Cited by 407 · see citing works
Self-citationHunter, 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
Tournebize, 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
Targeting, Capture, and Stabilization of Microtubules at Early Focal Adhesions
Kaverina, I., Rottner, K., & Small, J. V. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.142.1.181 · Cited by 323 · 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
Self-citationKinesin Superfamily Protein 2A (KIF2A) Functions in Suppression of Collateral Branch Extension
Homma, N., Takei, Y., Tanaka, Y., Nakata, T., Terada, S., Kikkawa, M., Noda, Y., & Hirokawa, N. (2003) · Cell · doi:10.1016/s0092-8674(03)00522-1 · Cited by 281 · see citing works
Kline-Smith, S. L., Khodjakov, A. L., Hergert, P. J., & Walczak, C. (2003) · Molecular Biology of the Cell · doi:10.1091/mbc.e03-08-0581 · Cited by 280 · see citing works
Regulation of leading edge microtubule and actin dynamics downstream of Rac1
Wittmann, T., Bokoch, G., & Waterman, C. M. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200303082 · Cited by 273 · see citing works
Cytoplasmic linker proteins promote microtubule rescue in vivo
Komarova, Y. A., Akhmanova, A. S., Kojima, S.-I., Galjart, N., & Borisy, G. G. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200208058 · Cited by 246 · see citing works
Yeast Bim1p Promotes the G1-specific Dynamics of Microtubules
Tirnauer, J. S., O'Toole, E. T., Berrueta, L., Bierer, B. E., & Pellman, D. S. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.145.5.993 · Cited by 245 · see citing works
Regulation of Microtubule Destabilizing Activity of Op18/Stathmin Downstream of Rac1
Wittmann, T., Bokoch, G., & Waterman, C. M. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m307261200 · Cited by 240 · 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
Regulation of microtubule-associated proteins
Cassimeris, L., & Spittle, C. S. (2001) · International review of cytology · doi:10.1016/s0074-7696(01)10006-9 · Cited by 220 · see citing works
Drosophila RhoGEF2 Associates with Microtubule Plus Ends in an EB1-Dependent Manner
Rogers, S. L., Wiedemann, U., Häcker, U., Turck, C. W., & Vale, R. D. (2004) · Current Biology · doi:10.1016/j.cub.2004.09.078 · Cited by 220 · see citing works
Self-citationOhi, 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
Carvalho, P., Gupta, M. L., Hoyt, M. A., & Pellman, D. S. (2004) · Developmental Cell · doi:10.1016/j.devcel.2004.05.001 · Cited by 219 · see citing works
Reconstitution of Physiological Microtubule Dynamics Using Purified Components
Kinoshita, K., Arnal, I., Desai, A. B., Drechsel, D. N., & Hyman, A. A. (2001) · Science · doi:10.1126/science.1064629 · Cited by 212 · see citing works
Microtubules meet substrate adhesions to arrange cell polarity
Small, J. V., & Kaverina, I. (2003) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(02)00008-x · Cited by 211 · see citing works
Tirnauer, J. S., Grego, S., Salmon, E. D., & Mitchison, T. J. (2002) · Molecular Biology of the Cell · doi:10.1091/mbc.e02-04-0210 · Cited by 207 · 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
Nanometer targeting of microtubules to focal adhesions
Krylyshkina, O., Anderson, K. I., Kaverina, I., Upmann, I., Manstein, D. J., Small, J. V., & Toomre, D. K. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200301102 · Cited by 167 · see citing works
The Microtubule-destabilizing Kinesin XKCM1 Regulates Microtubule Dynamic Instability in Cells
Kline-Smith, S. L., & Walczak, C. E. (2002) · Molecular Biology of the Cell · doi:10.1091/mbc.e01-12-0143 · Cited by 163 · 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 Kinesin-related Proteins, Kip2p and Kip3p, Function Differently in Nuclear Migration in Yeast
Miller, R. K., Heller, K. K., Frisèn, L., Wallack, D. L., Loayza, D., Gammie, A. E., & Rose, M. D. (1998) · Molecular Biology of the Cell · doi:10.1091/mbc.9.8.2051 · Cited by 140 · see citing works
Lantz, V., & Miller, K. G. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.140.4.897 · Cited by 135 · see citing works
Tea2p Kinesin Is Involved in Spatial Microtubule Organization by Transporting Tip1p on Microtubules
Busch, K. E., Hayles, J., Nurse, P., & Brunner, D. (2004) · Developmental Cell · doi:10.1016/j.devcel.2004.05.008 · Cited by 134 · see citing works
Targeted movement of cell end factors in fission yeast
Browning, H., Hackney, D. D., & Nurse, P. (2003) · Nature Cell Biology · doi:10.1038/ncb1034 · Cited by 124 · see citing works
Ohi, R., Coughlin, M. L., Lane, W. S., & Mitchison, T. J. (2003) · Developmental Cell · doi:10.1016/s1534-5807(03)00229-6 · Cited by 114 · see citing works
Tran, P. T., Walker, R. A., & Salmon, E. D. (1997) · The Journal of Cell Biology · doi:10.1083/jcb.138.1.105 · Cited by 107 · see citing works
K-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
A plus-end raft to control microtubule dynamics and function
Galjart, N., & Perez, F. (2003) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(02)00007-8 · Cited by 101 · see citing works
Holmfeldt, P., Stenmark, S., & Gullberg, M. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600076 · Cited by 87 · see citing works
TheDrosophilaKinesin-like Protein KLP67A Is Essential for Mitotic and Male Meiotic Spindle Assembly
Gandhi, R., Bonaccorsi, S., Bilodeau-Wentworth, D., Doxsey, S., Gatti, M., & Pereira, A. (2003) · Molecular Biology of the Cell · doi:10.1091/mbc.e03-05-0342 · Cited by 81 · 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
Flagged first, then by citations
1 of the 47 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
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
Super-resolution video microscopy of live cells by structured illumination
Kner, P., Chhun, B. B., Griffis, E. R., Winoto, L., & Gustafsson, M. G. L. (2009) · Nature Methods · doi:10.1038/nmeth.1324 · Cited by 732 · see citing works
The depolymerizing kinesin MCAK uses lattice diffusion to rapidly target microtubule ends
Helenius, J., Brouhard, G., Kalaidzidis, Y., Diez, S., & Howard, J. (2006) · Nature · doi:10.1038/nature04736 · Cited by 454 · 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
Gupta, M. L., Carvalho, P., Roof, D. M., & Pellman, D. S. (2006) · Nature Cell Biology · doi:10.1038/ncb1457 · Cited by 322 · see citing works
Understanding microtubule dynamics for improved cancer therapy
Honoré, S., Pasquier, E., & Braguer, D. (2005) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-005-5330-x · Cited by 321 · see citing works
Tracking Single Particles and Elongated Filaments with Nanometer Precision
Ruhnow, F., Zwicker, D., & Diez, S. (2011) · Biophysical Journal · doi:10.1016/j.bpj.2011.04.023 · Cited by 296 · 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
Polarized Transport of Frizzled along the Planar Microtubule Arrays in Drosophila Wing Epithelium
Shimada, Y., Yonemura, S., Ohkura, H., Strutt, D. I., & Uemura, T. (2006) · Developmental Cell · doi:10.1016/j.devcel.2005.11.016 · Cited by 285 · see citing works
Patronin Regulates the Microtubule Network by Protecting Microtubule Minus Ends
Goodwin, S. S., & Vale, R. D. (2010) · Cell · doi:10.1016/j.cell.2010.09.022 · Cited by 257 · see citing works
Self-citationMicrotubule Plus End: A Hub of Cellular Activities
Lansbergen, G. W. A., & Akhmanova, A. S. (2006) · Traffic · doi:10.1111/j.1600-0854.2006.00400.x · Cited by 235 · see citing works
Plus-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
Microtubule-severing enzymes at the cutting edge
Sharp, D. J., & Ross, J. L. (2012) · Journal of Cell Science · doi:10.1242/jcs.101139 · Cited by 214 · see citing works
Self-citationEB1 and EB3 Control CLIP Dissociation from the Ends of Growing Microtubules
Komarova, Y. A., Lansbergen, G. W. A., Galjart, N., Grosveld, F. G., Borisy, G. G., & Akhmanova, A. S. (2005) · Molecular Biology of the Cell · doi:10.1091/mbc.e05-07-0614 · Cited by 200 · see citing works
Slep, K. C., Rogers, S. L., Elliott, S. L., Ohkura, H., Kolodziej, P. A., & Vale, R. D. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200410114 · Cited by 197 · see citing works
Self-citationMolecular pathways regulating mitotic spindle orientation in animal cells
Lu, M. S., & Johnston, C. A. (2013) · Development · doi:10.1242/dev.087627 · Cited by 159 · see citing works
Regulation 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
Oda, Y., & Fukuda, H. (2013) · The Plant Cell · doi:10.1105/tpc.113.117853 · Cited by 159 · 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
Kinesin-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
Oda, Y., Iida, Y., Kondo, Y., & Fukuda, H. (2010) · Current Biology · doi:10.1016/j.cub.2010.05.038 · Cited by 152 · 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
The Schizosaccharomyces pombe EB1 Homolog Mal3p Binds and Stabilizes the Microtubule Lattice Seam
Sandblad, L., Busch, K. E., Tittmann, P., Gross, H., Brunner, D., & Hoenger, A. (2006) · Cell · doi:10.1016/j.cell.2006.11.025 · Cited by 145 · see citing works
MCAK associates with the tips of polymerizing microtubules
Moore, A. T., Rankin, K. E., von Dassow, G., Peris, L., Wagenbach, M., Ovechkina, Y., Andrieux, A., Job, D., & Wordeman, L. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200411089 · Cited by 141 · see citing works
Secondary cell wall patterning during xylem differentiation
Oda, Y., & Fukuda, H. (2011) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2011.10.005 · Cited by 140 · see citing works
Rogers, G. C., Rusan, N. M., Peifer, M. A., & Rogers, S. L. (2008) · Molecular Biology of the Cell · doi:10.1091/mbc.e07-10-1069 · Cited by 136 · see citing works
Self-citationCell Cycle-dependent Dynamics and Regulation of Mitotic Kinesins in Drosophila S2 Cells
Goshima, G., & Vale, R. D. (2005) · Molecular Biology of the Cell · doi:10.1091/mbc.e05-02-0118 · Cited by 132 · see citing works
Self-citationJankovics, F., & Brunner, D. (2006) · Developmental Cell · doi:10.1016/j.devcel.2006.07.014 · Cited by 130 · see citing works
Civelekoglu‐Scholey, G., Sharp, D. J., Mogilner, A., & Scholey, J. M. (2006) · Biophysical Journal · doi:10.1529/biophysj.105.078691 · Cited by 124 · see citing works
Self-citationZhang, D., Grode, K. D., Stewman, S. F., Díaz‐Valencia, J. D., Liebling, E. J., Rath, U., Riera, T., Currie, J. D., Buster, D. W., Asenjo, A. B., et al. (2011) · Nature Cell Biology · doi:10.1038/ncb2206 · Cited by 118 · see citing works
Self-citationZaoui, K., Benseddik, K., Daou, P., Salaün, D., & Badache, A. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1000975107 · Cited by 112 · see citing works
Kif18B interacts with EB1 and controls astral microtubule length during mitosis
Stout, J. R., Yount, A. L., Powers, J. A., LeBlanc, C., Ems-McClung, S. C., & Walczak, C. E. (2011) · Molecular Biology of the Cell · doi:10.1091/mbc.e11-04-0363 · Cited by 111 · 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
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
Mitotic force generators and chromosome segregation
Civelekoglu‐Scholey, G., & Scholey, J. M. (2010) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-010-0326-6 · Cited by 78 · see citing works
Poleward Tubulin Flux in Spindles: Regulation and Function in Mitotic Cells
Buster, D. W., Zhang, D., & Sharp, D. J. (2007) · Molecular Biology of the Cell · doi:10.1091/mbc.e06-11-0994 · Cited by 75 · see citing works
Self-citationFlagellar regeneration requires cytoplasmic microtubule depolymerization and kinesin-13
Wang, L., Piao, T., Cao, M., Qin, T., Huang, L., Deng, H., Mao, T., & Pan, J. (2013) · Journal of Cell Science · doi:10.1242/jcs.124255 · Cited by 76 · 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
Delgehyr, N., Rangone, H., Fu, J., Mao, G., Tom, B. D. M., Riparbelli, M. G., Callaini, G., & Glover, D. M. (2012) · Current Biology · doi:10.1016/j.cub.2012.01.046 · Cited by 67 · 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
Quantitative analysis of an anaphase B switch: predicted role for a microtubule catastrophe gradient
Cheerambathur, D. K., Civelekoglu‐Scholey, G., Brust‐Mascher, I., Sommi, P., Mogilner, A., & Scholey, J. M. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200611113 · Cited by 60 · see citing works
Life with eight flagella: flagellar assembly and division in Giardia
Dawson, S. C., & House, S. A. (2010) · Current Opinion in Microbiology · doi:10.1016/j.mib.2010.05.014 · Cited by 59 · see citing works
Tamura, N., & Draviam, V. M. (2012) · Open Biology · doi:10.1098/rsob.120132 · 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
Welburn, J. P. I., & Cheeseman, I. M. (2012) · Molecular Biology of the Cell · doi:10.1091/mbc.e12-03-0214 · Cited by 58 · see citing works
CLIP-170 Homologue and NUDE Play Overlapping Roles in NUDF Localization inAspergillus nidulans
Efimov, V. P., Zhang, J., & Xiang, X. (2006) · Molecular Biology of the Cell · doi:10.1091/mbc.e05-11-1084 · Cited by 58 · see citing works
Ma, D., Wang, D., & Yang, W. (2017) · Biology of Reproduction · doi:10.1095/biolreprod.116.144113 · Cited by 58 · see citing works
Building the Microtubule Cytoskeleton Piece by Piece
Alfaro-Aco, R., & Petry, S. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.r115.638452 · Cited by 56 · see citing works
Structure of the Kinesin13-Microtubule Ring Complex
Tan, D., Rice, W. J., & Sosa, H. (2008) · Structure · doi:10.1016/j.str.2008.08.017 · Cited by 56 · see citing works
Kinesin-13s form rings around microtubules
Tan, D., Asenjo, A. B., Mennella, V., Sharp, D. J., & Sosa, H. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200605194 · Cited by 55 · 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
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
Five factors can reconstitute all three phases of microtubule polymerization dynamics
Moriwaki, T., & Goshima, G. (2016) · The Journal of Cell Biology · doi:10.1083/jcb.201604118 · Cited by 53 · see citing works
Reconstitution of dynamic microtubules with Drosophila XMAP215, EB1, and Sentin
Li, W., Moriwaki, T., Tani, T., Watanabe, T., Kaibuchi, K., & Goshima, G. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201206101 · Cited by 52 · see citing works
Competition between kinesin-1 and myosin-V defines Drosophila posterior determination
Lü, W., Lakonishok, M., Liu, R., Billington, N., Rich, A., Glotzer, M., Sellers, J. R., & Gelfand, V. I. (2020) · eLife · doi:10.7554/elife.54216 · Cited by 52 · see citing works
Costal2 Functions as a Kinesin-like Protein in the Hedgehog Signal Transduction Pathway
Farzan, S. F., Ascano, M., Ogden, S. K., Sanial, M., Brigui, A., Plessis, A., & Robbins, D. J. (2008) · Current Biology · doi:10.1016/j.cub.2008.07.026 · Cited by 52 · see citing works
Tao-1 is a negative regulator of microtubule plus-end growth
Liu, T., Rohn, J. L., Picone, R., Kunda, P. E., & Baum, B. (2010) · Journal of Cell Science · doi:10.1242/jcs.068726 · Cited by 51 · 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
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
Silverman-Gavrila, R., & Wilde, A. (2006) · Molecular Biology of the Cell · doi:10.1091/mbc.e05-10-0991 · Cited by 47 · see citing works
Functional Characterisation and Drug Target Validation of a Mitotic Kinesin-13 in Trypanosoma brucei
Chan, K. Y., Matthews, K. R., & Ersfeld, K. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1001050 · Cited by 46 · see citing works
Tai, C.-J., Shen, S., Lee, W.-R., Liao, C., Deng, W., Chiou, H., Hsieh, C.-I., Tung, J.-N., Chen, C.-S., Chiou, J.-F., et al. (2010) · Experimental Cell Research · doi:10.1016/j.yexcr.2010.07.019 · Cited by 44 · see citing works
An Improved Optical Tweezers Assay for Measuring the Force Generation of Single Kinesin Molecules
Nicholas, M. P., Rao, L., & Gennerich, A. (2014) · Methods in molecular biology · doi:10.1007/978-1-4939-0329-0_10 · Cited by 41 · 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
Talapatra, S. K., Harker, B., & Welburn, J. P. I. (2015) · eLife · doi:10.7554/elife.06421 · Cited by 39 · see citing works
Emergent Properties of the Metaphase SpindlePreprint
Reber, S., & Hyman, A. A. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a015784 · Cited by 39 · 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
A 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
Alternative cytoskeletal landscapes: cytoskeletal novelty and evolution in basal excavate protists
Dawson, S. C., & Paredez, A. R. (2013) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2012.11.005 · Cited by 34 · see citing works
Zheng, Y., Mennella, V., Marks, S., Wildonger, J., Elnagdi, E., Agard, D. A., & Megraw, T. L. (2016) · Molecular Biology of the Cell · doi:10.1091/mbc.e15-09-0655 · Cited by 34 · see citing works
Self-citationKinesin-13 regulates the quantity and quality of tubulin inside cilia
Vasudevan, K. K., Jiang, Y., Lechtreck, K. F., Kushida, Y., Alford, L. M., Sale, W. S., Hennessey, T. M., & Gaertig, J. (2014) · Molecular Biology of the Cell · doi:10.1091/mbc.e14-09-1354 · Cited by 33 · see citing works
A nuclear-derived proteinaceous matrix embeds the microtubule spindle apparatus during mitosis
Yao, C., Rath, U., Maiato, H., Sharp, D., Girton, J. R., Johansen, K. M., & Johansen, J. (2012) · Molecular Biology of the Cell · doi:10.1091/mbc.e12-06-0429 · Cited by 32 · see citing works
Self-citationThe Drosophila Kinesin-13, KLP59D, Impacts Pacman- and Flux-based Chromosome Movement
Rath, U., Rogers, G. C., Tan, D., Gómez-Ferrerı́a, M. A., Buster, D. W., Sosa, H., & Sharp, D. J. (2009) · Molecular Biology of the Cell · doi:10.1091/mbc.e09-07-0557 · Cited by 32 · see citing works
Self-citationKinesin-13 and Kinesin-8 Function during Cell Growth and Division in the Moss Physcomitrella patens
Leong, S. Y., Edzuka, T., Goshima, G., & Yamada, M. (2020) · The Plant Cell · doi:10.1105/tpc.19.00521 · 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
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
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
Self-citationA microtubule polymerase is required for microtubule orientation and dendrite pruning in Drosophila
Tang, Q., Rui, M., Bu, S., Wang, Y., Chew, L. Y., & Yu, F. (2020) · The EMBO Journal · doi:10.15252/embj.2019103549 · Cited by 27 · see citing works
Stable and dynamic microtubules coordinately determine and maintain Drosophila bristle shape
Bitan, A., Rosenbaum, I., & Abdu, U. (2012) · Development · doi:10.1242/dev.076893 · Cited by 27 · see citing works
KIF2A deficiency causes early-onset neurodegeneration
Ruiz-Reig, N., Chehade, G., Hakanen, J., Aittaleb, M., Wierda, K. D. B., de Wit, J., Nguyen, L., Gailly, P. L., & Tissir, F. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2209714119 · Cited by 24 · see citing works
Promoting microtubule assembly: A hypothesis for the functional significance of the +TIP network
Gupta, K. K., Alberico, E. O., Näthke, I. S., & Goodson, H. V. (2014) · BioEssays · doi:10.1002/bies.201400029 · 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
Iimori, M., Ozaki, K., Chikashige, Y., Habu, T., Hiraoka, Y., Maki, T., Hayashi, I., Obuse, C., & Matsumoto, T. (2011) · Experimental Cell Research · doi:10.1016/j.yexcr.2011.11.006 · Cited by 23 · see citing works
A microtubule-destabilizing kinesin motor regulates spindle length and anchoring in oocytes
Zou, J., Hallen, M. A., Yankel, C. D., & Endow, S. A. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200711031 · Cited by 23 · see citing works
Direct Regulation of Microtubule Dynamics by KIF17 Motor and Tail Domains
Acharya, B. R., Espenel, C., & Kreitzer, G. E. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.494989 · Cited by 22 · see citing works
Motion tracking of the outer tips of microtubules
Hadjidemetriou, S., Toomre, D. K., & Duncan, J. S. (2008) · Medical Image Analysis · doi:10.1016/j.media.2008.04.004 · Cited by 21 · see citing works
DHTP is an allosteric inhibitor of the kinesin‐13 family of microtubule depolymerases
Talje, L., Kadhi, K. B. E., Atchia, K., Tremblay-Boudreault, T., Carreno, S., & Kwok, B. H. B. (2014) · FEBS Letters · doi:10.1016/j.febslet.2014.05.024 · Cited by 18 · see citing works
Lü, W., Lakonishok, M., & Gelfand, V. I. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2303376120 · Cited by 17 · see citing works
A Second Tubulin Binding Site on the Kinesin-13 Motor Head Domain Is Important during Mitosis
Zhang, D., Asenjo, A. B., Greenbaum, M., Xie, L., Sharp, D. J., & Sosa, H. (2013) · PLoS ONE · doi:10.1371/journal.pone.0073075 · Cited by 17 · see citing works
Self-citationTransformation of Drosophila Cell Lines
Cherbas, L., & Cherbas, P. T. (2007) · Methods in molecular biology · doi:10.1007/978-1-59745-457-5_16 · Cited by 17 · see citing works
Schimizzi, G. V., Currie, J. D., & Rogers, S. L. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011381 · Cited by 16 · see citing works
Self-citationLuo, R., Reed, C. E., Sload, J. A., Wordeman, L. G., Randazzo, P. A., & Chen, P.-W. (2017) · Small GTPases · doi:10.1080/21541248.2017.1308850 · Cited by 15 · see citing works
Organization of microtubule plus-end dynamics by phase separation in mitosis
Yang, F., Ding, M., Song, X., Chen, F., Yang, T., Wang, C., Hu, C., Hu, Q. S., Yao, Y., Du, S., et al. (2024) · Journal of Molecular Cell Biology · doi:10.1093/jmcb/mjae006 · Cited by 13 · see citing works
Septins guide noncentrosomal microtubules to promote focal adhesion disassembly in migrating cells
Merenich, D., Νάκος, Κ., Pompan, T., Donovan, S. J., Gill, A., Patel, P., Spiliotis, E. T., & Myers, K. A. (2022) · Molecular Biology of the Cell · doi:10.1091/mbc.e21-06-0334 · Cited by 13 · see citing works
Gottardo, M., Callaini, G., & Riparbelli, M. G. (2016) · Cell Cycle · doi:10.1080/15384101.2016.1248005 · Cited by 13 · see citing works
- Authors
- Mennella, V., Rogers, G. C., Rogers, S. L., Buster, D. W., Vale, R. D., & Sharp, D. J.
- Affiliations
- Albert Einstein College of Medicine (US)
- Howard Hughes Medical Institute (US)
- Corresponding author
- Sharp, David J.
- Venue
- Nature Cell Biology
- Published
- 2005-02-20
- Volume
- 7
- Issue
- 3
- Pages
- 235-245
- ISSN
- 1465-7392 (ISSN-L)
- 1476-4679
- OpenAlex
- W2134553114
- Cited by
- 154
- References
- 47
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 4 · 2023: 4 · 2022: 13 · 2021: 2 · 2020: 5 · 2019: 3 · 2018: 2 · 2017: 2 · 2016: 8 · 2015: 6 · 2014: 7 · 2013: 8 · 2012: 13
- FWCI
- 5.29
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- ePrints Soton (University of Southampton) (submittedVersion)
- Funders
- Leukemia and Lymphoma Society
- National Institutes of Health
- Albert Einstein College of Medicine, Yeshiva University
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Health Sciences › Medicine › Oncology › Cancer Treatment and Pharmacology
- Keywords
- kinesin-13, microtubule dynamics, microtubule depolymerization, dynamic instability, catastrophe, rescue, EB1, interphase, Drosophila melanogaster, S2 cells
- MeSH terms
- Animals, Cell Line, Drosophila, Drosophila melanogaster, Glutathione Transferase, Interphase, Microscopy, Fluorescence, Microtubules, Models, Biological, Polymers, RNA, Double-Stranded, Time Factors, Blotting, Western, Kinesins, Protein Structure, Tertiary, RNA Interference, 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