Anillin binds nonmuscle myosin II and regulates the contractile ring
Open accessAbstract
We demonstrate that the contractile ring protein anillin interacts directly with nonmuscle myosin II and that this interaction is regulated by myosin light chain phosphorylation. We show that despite their interaction, anillin and myosin II are independently targeted to the contractile ring. Depletion of anillin in Drosophila or human cultured cells results in cytokinesis failure. Human cells depleted for anillin fail to properly regulate contraction by myosin II late in cytokinesis and fail in abscission. We propose a role for anillin in spatially regulating the contractile activity of myosin II during cytokinesis.
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Anillin is delivered to the CCF where it normally binds to both Myosin II and Septin.
“Anillin is delivered to the CCF where it normally binds to both Myosin II and Septin [20, 25]”
From Tumor Treating Fields Perturb the Localization of Septins and Cause Aberrant Mitotic Exit (2015) · cites this paper as [25]
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Cites
Phosphorylation and Activation of Myosin by Rho-associated Kinase (Rho-kinase)
Amano, M., Ito, M., Kimura, K., Fukata, Y., Chihara, K., Nakano, T., Matsuura, Y., & Kaibuchi, K. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.34.20246 · Cited by 2,009 · see citing works
Dissecting temporal and spatial control of cytokinesis with a myosin II Inhibitor
Straight, A. F., Cheung, A., Limouze, J., Chen, I., Westwood, N. J., Sellers, J. R., & Mitchison, T. J. (2003) · Science · doi:10.1126/science.1081412 · Cited by 1,412 · see citing works
Self-citation[18] Purification of muscle actin
Pardee, J. D., & Aspudich, J. (1982) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(82)85020-9 · Cited by 1,190 · see citing works
Murray, A. W. (2004) · Cell · doi:10.1016/s0092-8674(03)01080-8 · Cited by 1,054 · see citing works
Disruption of the Dictyostelium Myosin Heavy Chain Gene by Homologous Recombination
Lozanne, A. D., & Spudich, J. A. (1987) · Science · doi:10.1126/science.3576222 · Cited by 988 · see citing works
Chapter 30 Cell Cycle Extracts
Murray, A. W. (1991) · Methods in cell biology · doi:10.1016/s0091-679x(08)60298-8 · Cited by 942 · see citing works
Antisense RNA Inactivation of Myosin Heavy Chain Gene Expression in Dictyostelium discoideum
Knecht, D. A., & Loomis, W. F. (1987) · Science · doi:10.1126/science.3576221 · Cited by 679 · see citing works
Self- and actin-templated assembly of Mammalian septins
Kinoshita, M., Field, C. M., Coughlin, M. L., Straight, A. F., & Mitchison, T. J. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00366-0 · Cited by 526 · see citing works
Anillin, a contractile ring protein that cycles from the nucleus to the cell cortex.
Field, C. M., & Alberts, B. (1995) · The Journal of Cell Biology · doi:10.1083/jcb.131.1.165 · Cited by 440 · see citing works
Murray, A. W. (1991) · PubMed · Cited by 438 · see citing works
The effect of myosin antibody on the division of starfish blastomeres
Mabuchi, I., & Okuno, M. (1977) · The Journal of Cell Biology · doi:10.1083/jcb.74.1.251 · Cited by 437 · see citing works
Wu, J., Kuhn, J. R., Kovar, D. R., & Pollard, T. D. (2003) · Developmental Cell · doi:10.1016/s1534-5807(03)00324-1 · Cited by 391 · see citing works
RAPPAPORT, R. (1990) · Springer eBooks · doi:10.1007/978-3-642-83631-2_1 · Cited by 364 · see citing works
Polo-like kinases: positive regulators of cell division from start to finish
Nigg, E. A. (1998) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(98)80121-x · Cited by 344 · see citing works
Glotzer, M. (2001) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.17.1.351 · Cited by 342 · see citing works
Role of Polo Kinase and Mid1p in Determining the Site of Cell Division in Fission Yeast
Bähler, J., Steever, A. B., Wheatley, S. P., Wang, Y.-L., Pringle, J. R., Gould, K. L., & McCollum, D. (1998) · The Journal of Cell Biology · doi:10.1083/jcb.143.6.1603 · Cited by 315 · see citing works
Oegema, K., Savoian, M. S., Mitchison, T. J., & Field, C. M. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.150.3.539 · Cited by 309 · see citing works
The dmf1/mid1 gene is essential for correct positioning of the division septum in fission yeast.Preprint
Sohrmann, M., Fankhauser, C., Brodbeck, C., & Simanis, V. (1996) · Genes & Development · doi:10.1101/gad.10.21.2707 · Cited by 252 · see citing works
Félix, M., Cohen, P., & Karsenti, E. (1990) · The EMBO Journal · doi:10.1002/j.1460-2075.1990.tb08159.x · Cited by 248 · see citing works
Molecular Dissection of Cytokinesis by RNA Interference inDrosophilaCultured Cells
Somma, M. P., Fasulo, B., Cenci, G., Cundari, E., & Gatti, M. (2002) · Molecular Biology of the Cell · doi:10.1091/mbc.01-12-0589 · Cited by 240 · see citing works
Cytokinesis in eukaryotes: a mechanistic comparison
Field, C. M., Li, R., & Oegema, K. (1999) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(99)80009-x · Cited by 239 · see citing works
[30] Smooth muscle myosin light chain kinase
Walsh, M. P., Hinkins, S., Dąbrowska, R., & Hartshorne, D. J. (1983) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(83)99063-8 · Cited by 226 · see citing works
RAPPAPORT, R. (1996) · Cambridge University Press eBooks · doi:10.1017/cbo9780511529764 · Cited by 208 · see citing works
Paoletti, A., & Chang, F. (2000) · Molecular Biology of the Cell · doi:10.1091/mbc.11.8.2757 · Cited by 205 · see citing works
Yamashiro, S., Totsukawa, G., Yamakita, Y., Sasaki, Y., Madaule, P., Ishizaki, T., Narumiya, S., & Matsumura, F. (2003) · Molecular Biology of the Cell · doi:10.1091/mbc.e02-07-0427 · Cited by 202 · see citing works
Microtubules, membranes and cytokinesis
Straight, A. F., & Field, C. M. (2000) · Current Biology · doi:10.1016/s0960-9822(00)00746-6 · Cited by 189 · see citing works
Self-citationKelley, C. A., Sellers, J. R., Gard, D. L., Bui, D., Adelstein, R. S., & Baines, I. (1996) · The Journal of Cell Biology · doi:10.1083/jcb.134.3.675 · Cited by 163 · see citing works
Tasto, J. J., Morrell‐Falvey, J. L., & Gould, K. L. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200211126 · Cited by 158 · see citing works
In vivo phosphorylation of regulatory light chain of myosin II during mitosis of cultured cells
Yamakita, Y., Yamashiro, S., & Matsumura, F. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.124.1.129 · Cited by 155 · see citing works
Mid2p stabilizes septin rings during cytokinesis in fission yeast
Berlin, A., Paoletti, A., & Chang, F. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200212016 · Cited by 155 · see citing works
Pinder, J. C., Fowler, R. E., Dluzewski, A. R., Bannister, L. H., Lavin, F. M., Mitchell, G. H., Wilson, R. J., & Gratzer, W. B. (1998) · Journal of Cell Science · doi:10.1242/jcs.111.13.1831 · Cited by 143 · see citing works
Motegi, F., Mishra, M., Balasubramanian, M. K., & Mabuchi, I. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200402097 · Cited by 119 · see citing works
Sellers, J. R. (1999) · doi:10.1093/oso/9780198505099.001.0001 · Cited by 96 · see citing works
Baculovirus Expression of Chicken Nonmuscle Heavy Meromyosin II-B
Pato, M. D., Sellers, J. R., Preston, Y. A., Harvey, E. V., & Adelstein, R. S. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.5.2689 · Cited by 68 · see citing works
src64andtec29are required for microfilament contraction duringDrosophilacellularization
Thomas, J. H., & Wieschaus, E. F. (2004) · Development · doi:10.1242/dev.00989 · Cited by 64 · see citing works
A Conserved Negatively Charged Amino Acid Modulates Function in Human Nonmuscle Myosin IIA
Wang, F., Harvey, E. V., Conti, M. A., Wei, D., & Sellers, J. R. (2000) · Biochemistry · doi:10.1021/bi000133x · Cited by 62 · see citing works
Purification and characterization of platelet myosin
Daniel, J. L., & Sellers, J. R. (1992) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(92)15054-g · Cited by 39 · see citing works
Wheatley, S. P., O’Connell, C. B., & Wang, Y. (1998) · Molecular Biology of the Cell · doi:10.1091/mbc.9.8.2173 · Cited by 32 · see citing works
Mansfield, G. S., Al-Shirawi, D. Y., Ketchum, A., Newbern, C. E., & Kiehart, D. P. (1996) · Journal of Molecular Biology · doi:10.1006/jmbi.1996.0009 · Cited by 32 · see citing works
[31] Purification of nonmuscle myosins
Pollard, T. D. (1982) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(82)85033-7 · Cited by 29 · see citing works
Differential expression of non-muscle myosin heavy chain genes during Xenopus embryogenesis
Bhatia‐Dey, N., Taira, M., Conti, M. A., Nooruddin, H., & Adelstein, R. S. (1998) · Mechanisms of Development · doi:10.1016/s0925-4773(98)00136-1 · Cited by 16 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- Sellers, J. R. (1999). Myosins, Oxford, NY: Oxford University Press.
Cited by
Sorted by citations
The Molecular Requirements for Cytokinesis
Glotzer, M. (2005) · Science · doi:10.1126/science.1096896 · Cited by 710 · see citing works
Reassembly of contractile actin cortex in cell blebs
Charras, G., Hu, C., Coughlin, M. L., & Mitchison, T. J. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200602085 · Cited by 620 · see citing works
Green, R. A., Paluch, E. K., & Oegema, K. (2012) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-101011-155718 · Cited by 560 · see citing works
Regulation of the Actin Cytoskeleton-Plasma Membrane Interplay by Phosphoinositides
Saarikangas, J., Zhao, H., & Lappalainen, P. (2010) · Physiological Reviews · doi:10.1152/physrev.00036.2009 · Cited by 495 · see citing works
Animal Cytokinesis: From Parts List to Mechanisms
Eggert, U., Mitchison, T. J., & Field, C. M. (2006) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.74.082803.133425 · Cited by 439 · see citing works
Anillin is a scaffold protein that links RhoA, actin, and myosin during cytokinesis
Piekny, A. J., & Glotzer, M. (2008) · Current Biology · doi:10.1016/j.cub.2007.11.068 · Cited by 426 · see citing works
Regulation of myosin II during cytokinesis in higher eukaryotes
Matsumura, F. (2005) · Trends in Cell Biology · doi:10.1016/j.tcb.2005.05.004 · Cited by 416 · see citing works
Polar actomyosin contractility destabilizes the position of the cytokinetic furrow
Sedzinski, J., Biro, M., Oswald, A., Tinévez, J.-Y., Salbreux, G., & Paluch, E. K. (2011) · Nature · doi:10.1038/nature10286 · Cited by 339 · see citing works
Actin cytoskeleton dynamics and the cell division cycle
Heng, Y.-W., & Koh, C.-G. (2010) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2010.04.007 · Cited by 280 · see citing works
Myosin-II-Dependent Localization and Dynamics of F-Actin during Cytokinesis
Murthy, K., & Wadsworth, P. (2005) · Current Biology · doi:10.1016/j.cub.2005.02.055 · Cited by 282 · see citing works
The myriad roles of Anillin during cytokinesis
Piekny, A. J., & Maddox, A. S. (2010) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2010.08.002 · Cited by 271 · see citing works
Cortical Dynein and Asymmetric Membrane Elongation Coordinately Position the Spindle in Anaphase
Kiyomitsu, T., & Cheeseman, I. M. (2013) · Cell · doi:10.1016/j.cell.2013.06.010 · Cited by 263 · see citing works
Midbody assembly and its regulation during cytokinesis
Hu, C., Coughlin, M. L., & Mitchison, T. J. (2012) · Molecular Biology of the Cell · doi:10.1091/mbc.e11-08-0721 · Cited by 260 · see citing works
Proteomic screen defines the Polo‐box domain interactome and identifies Rock2 as a Plk1 substrate
Lowery, D. M., Clauser, K. R., Hjerrild, M., Lim, D., Alexander, J., Kishi, K., Ong, S., Gammeltoft, S., Carr, S. A., & Yaffe, M. B. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601683 · Cited by 258 · see citing works
Burkard, M. E., Randall, C. L., Larochelle, S., Zhang, C., Shokat, K. M., Fisher, R. P., & Jallepalli, P. V. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0701140104 · Cited by 252 · see citing works
Zhao, W.-M., Seki, A., & Fang, G. (2006) · Molecular Biology of the Cell · doi:10.1091/mbc.e06-01-0015 · Cited by 244 · see citing works
Distinct roles of septins in cytokinesis: SEPT9 mediates midbody abscission
Estey, M. P., Di Ciano-Oliveira, C., Froese, C. D., Bejide, M. T., & Trimble, W. S. (2010) · Journal of Cell Biology · doi:10.1083/jcb.201006031 · Cited by 231 · see citing works
Nonmuscle myosin-2: mix and match
Heissler, S. M., & Manstein, D. J. (2012) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-012-1002-9 · Cited by 225 · see citing works
Mammalian SEPT2 Is Required for Scaffolding Nonmuscle Myosin II and Its Kinases
Joo, E. E., Surka, M. C., & Trimble, W. S. (2007) · Developmental Cell · doi:10.1016/j.devcel.2007.09.001 · Cited by 227 · see citing works
Some assembly required: yeast septins provide the instruction manual
Versele, M., & Thorner, J. W. (2005) · Trends in Cell Biology · doi:10.1016/j.tcb.2005.06.007 · Cited by 227 · see citing works
Anillin and the Septins Promote Asymmetric Ingression of the Cytokinetic Furrow
Maddox, A. S., Lewellyn, L., Desai, A. B., & Oegema, K. (2007) · Developmental Cell · doi:10.1016/j.devcel.2007.02.018 · Cited by 212 · see citing works
CENP-C recruits M18BP1 to centromeres to promote CENP-A chromatin assembly
Moree, B., Meyer, C. B., Fuller, C. J., & Straight, A. F. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201106079 · Cited by 218 · see citing works
Self-citationTumor Treating Fields Perturb the Localization of Septins and Cause Aberrant Mitotic Exit
Gera, N., Yang, A., Holtzman, T. S., Lee, S. X., Wong, E. T., & Swanson, K. D. (2015) · PLOS ONE · doi:10.1371/journal.pone.0125269 · Cited by 217 · see citing works
Cleavage furrow formation and ingression during animal cytokinesis: a microtubule legacy
D’Avino, P. P., Savoian, M. S., & Glover, D. M. (2005) · Journal of Cell Science · doi:10.1242/jcs.02335 · Cited by 190 · see citing works
Watanabe, S., Ando, Y., Yasuda, S., Hosoya, H., Watanabe, N., Ishizaki, T., & Narumiya, S. (2008) · Molecular Biology of the Cell · doi:10.1091/mbc.e07-10-1086 · Cited by 183 · see citing works
Distinct roles for two C. elegans anillins in the gonad and early embryo
Maddox, A. S., Habermann, B. H., Desai, A. B., & Oegema, K. (2005) · Development · doi:10.1242/dev.01828 · Cited by 177 · see citing works
Assembly and architecture of precursor nodes during fission yeast cytokinesis
Laporte, D., Coffman, V. C., Lee, I., & Wu, J. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201008171 · Cited by 178 · see citing works
Kinoshita, M. (2005) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2005.12.005 · Cited by 174 · see citing works
Understanding Cytokinesis Failure
Normand, G., & King, R. W. (2010) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-6199-0_3 · Cited by 171 · see citing works
Cytokinetic abscission: cellular dynamics at the midbody
Steigemann, P., & Gerlich, D. W. (2009) · Trends in Cell Biology · doi:10.1016/j.tcb.2009.07.008 · Cited by 162 · see citing works
Microtubules and actin crosstalk in cell migration and division
Akhshi, T. K., Wernike, D., & Piekny, A. J. (2013) · Cytoskeleton · doi:10.1002/cm.21150 · Cited by 157 · see citing works
Field, C. M., Coughlin, M., Doberstein, S., Marty, T., & Sullivan, W. (2005) · Development · doi:10.1242/dev.01843 · Cited by 156 · see citing works
Self-citationAnillin localization defect in cardiomyocyte binucleation
Engel, F. B., Schebesta, M., & Keating, M. T. (2006) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2006.06.012 · Cited by 154 · see citing works
Anillin Acts as a Bifunctional Linker Coordinating Midbody Ring Biogenesis during Cytokinesis
Kechad, A., Jananji, S., Ruella, Y., & Hickson, G. R. X. (2012) · Current Biology · doi:10.1016/j.cub.2011.11.062 · Cited by 150 · see citing works
Regulation of the actin cytoskeleton by PIP2 in cytokinesis
Logan, M. R., & Mandato, C. A. (2006) · Biology of the Cell · doi:10.1042/bc20050081 · Cited by 144 · see citing works
Gregory, S. L., Ebrahimi, S., Milverton, J. L., Jones, W. M., Bejsovec, A., & Saint, R. B. (2008) · Current Biology · doi:10.1016/j.cub.2007.11.050 · Cited by 143 · see citing works
Zhao, W.-M., & Fang, G. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m504657200 · Cited by 143 · see citing works
Conversion of midbodies into germ cell intercellular bridges
Greenbaum, M. P., Ma, L., & Matzuk, M. M. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.02.025 · Cited by 137 · see citing works
Rho-dependent control of anillin behavior during cytokinesis
Hickson, G. R. X., & O’Farrell, P. H. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200709005 · Cited by 138 · see citing works
Tuning the Poisson's Ratio of Biomaterials for Investigating Cellular Response
Zhang, W., Soman, P., Meggs, K., Qu, X., & Chen, S. (2013) · Advanced Functional Materials · doi:10.1002/adfm.201202666 · Cited by 138 · see citing works
Polo-Like Kinase Controls Vertebrate Spindle Elongation and Cytokinesis
Brennan, I. M., Peters, U., Kapoor, T. M., & Straight, A. F. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000409 · Cited by 135 · see citing works
Self-citationMechanistic Insights into the Anchorage of the Contractile Ring by Anillin and Mid1
Sun, L., Guan, R., Lee, I., Liu, Y., Chen, M., Wang, J., Wu, J., & Chen, Z. (2015) · Developmental Cell · doi:10.1016/j.devcel.2015.03.003 · Cited by 129 · see citing works
Citron kinase controls abscission through RhoA and anillin
Gai, M., Camera, P., Dema, A., Bianchi, F. T., Berto, G. E., Scarpa, E., Germena, G., & Cunto, F. D. (2011) · Molecular Biology of the Cell · doi:10.1091/mbc.e10-12-0952 · Cited by 126 · see citing works
D’Avino, P. P., Takeda, T., Capalbo, L., Zhang, W., Lilley, K. S., Laue, E. D., & Glover, D. M. (2008) · Journal of Cell Science · doi:10.1242/jcs.026716 · Cited by 129 · see citing works
How to scaffold the contractile ring for a safe cytokinesis – lessons from Anillin-related proteins
D’Avino, P. P. (2009) · Journal of Cell Science · doi:10.1242/jcs.034785 · Cited by 127 · see citing works
Dynamic positioning of the fission yeast cell division plane
Daga, R. R., & Chang, F. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0409021102 · Cited by 126 · see citing works
Features of cardiomyocyte proliferation and its potential for cardiac regeneration
van Amerongen, M. J., & Engel, F. B. (2008) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2008.00439.x · Cited by 126 · see citing works
Cleavage Furrow Organization Requires PIP2-Mediated Recruitment of Anillin
Liu, J., Fairn, G. D., Ceccarelli, D. F. J., Sicheri, F., & Wilde, A. (2011) · Current Biology · doi:10.1016/j.cub.2011.11.040 · Cited by 120 · see citing works
Spatial organization of cytokinesis signaling reconstituted in a cell-free system
Nguyen, P. A. H., Groen, A. C., Loose, M., Ishihara, K., Wühr, M., Field, C. M., & Mitchison, T. J. (2014) · Science · doi:10.1126/science.1256773 · Cited by 120 · see citing works
Reyes, C., Jin, M., Breznau, E. B., Espino, R., Delgado-Gonzalo, R., Goryachev, A. B., & Miller, A. L. (2014) · Current Biology · doi:10.1016/j.cub.2014.04.021 · Cited by 113 · see citing works
Bao, J., Jana, S. S., & Adelstein, R. S. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m501573200 · Cited by 116 · see citing works
Laplante, C., Huang, F., Tebbs, I. R., Bewersdorf, J., & Pollard, T. D. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1608252113 · Cited by 115 · see citing works
Leone, M., Magadum, A., & Engel, F. B. (2015) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00559.2015 · Cited by 113 · see citing works
Distinct Pathways for the Early Recruitment of Myosin II and Actin to the Cytokinetic Furrow
Zhou, M., & Wang, Y. (2007) · Molecular Biology of the Cell · doi:10.1091/mbc.e07-08-0783 · Cited by 114 · see citing works
Knockdown of ANLN by lentivirus inhibits cell growth and migration in human breast cancer
Zhou, W., Wang, Z., Shen, N., Pi, W., Jiang, W., Huang, J., Hu, Y., Xiong, L., & Sun, L. (2014) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-014-2200-6 · Cited by 108 · see citing works
Reversine increases the plasticity of lineage-committed mammalian cells
Chen, S., Takanashi, S., Zhang, Q., Xiong, W., Zhu, S., Peters, E. C., Ding, S., & Schultz, P. G. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0704360104 · Cited by 103 · see citing works
The Septin-Binding Protein Anillin Is Overexpressed in Diverse Human Tumors
Hall, P. A., Todd, C. B., Hyland, P. L., McDade, S. S., Grabsch, H. I., Dattani, M., Hillan, K. J., & Russell, S. E. H. (2005) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-05-0997 · Cited by 102 · see citing works
Anillin Promotes Cell Contractility by Cyclic Resetting of RhoA Residence Kinetics
Budnar, S., Husain, K. B., Gomez, G. A., Naghibosadat, M., Varma, A., Verma, S., Hamilton, N., Morris, R. G., & Yap, A. S. (2019) · Developmental Cell · doi:10.1016/j.devcel.2019.04.031 · Cited by 98 · see citing works
Schwayer, C., Sikora, M., Slováková, J., Kardos, R., & Heisenberg, C. (2016) · Developmental Cell · doi:10.1016/j.devcel.2016.05.024 · Cited by 95 · see citing works
Rho and Anillin-dependent Control of mDia2 Localization and Function in Cytokinesis
Watanabe, S., Okawa, K., Miki, T., Sakamoto, S., Morinaga, T., Segawa, K., Arakawa, T., Kinoshita, M., Ishizaki, T., & Narumiya, S. (2010) · Molecular Biology of the Cell · doi:10.1091/mbc.e10-04-0324 · Cited by 95 · see citing works
Magnusson, K., Gremel, G., Rydén, L., Pontén, V., Uhlén, M., Dimberg, A., Jirström, K., & Pontén, F. (2016) · BMC Cancer · doi:10.1186/s12885-016-2923-8 · Cited by 93 · see citing works
Sánchez‐Díaz, A., Marchesi, V., Murray, S., Jones, R. C., Pereira, G., Edmondson, R. D., Allen, T., & Labib, K. P. M. (2008) · Nature Cell Biology · doi:10.1038/ncb1701 · 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
An anillin-Ect2 complex stabilizes central spindle microtubules at the cortex during cytokinesis
Frenette, P., Haines, E., Loloyan, M., Kinal, M., Pakarian, P., & Piekny, A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0034888 · Cited by 86 · see citing works
Amini, R., Goupil, E., Labella, S., Zetka, M., Maddox, A. S., Labbé, J.-C., & Chartier, N. T. (2014) · The Journal of Cell Biology · doi:10.1083/jcb.201310117 · Cited by 86 · see citing works
Geddis, A. E., Fox, N. E., Tkachenko, E., & Kaushansky, K. (2007) · Cell Cycle · doi:10.4161/cc.6.4.3836 · Cited by 86 · see citing works
Overexpression of Anillin (ANLN) is correlated with colorectal cancer progression and poor prognosis
Wang, G., Shen, W., Cui, L., Chen, W., Hu, X., & Fu, J. (2016) · Cancer Biomarkers · doi:10.3233/cbm-160585 · Cited by 85 · see citing works
Cytokinesis in Metazoa and FungiPreprint
Glotzer, M. (2016) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a022343 · Cited by 83 · see citing works
Amine, N. E., Kechad, A., Jananji, S., & Hickson, G. R. X. (2013) · The Journal of Cell Biology · doi:10.1083/jcb.201305053 · Cited by 83 · see citing works
Identification of hub genes to regulate breast cancer metastasis to brain by bioinformatics analyses
Tang, D., Zhao, X., Zhang, L., Wang, Z. P., & Wang, C. (2018) · Journal of Cellular Biochemistry · doi:10.1002/jcb.28228 · Cited by 82 · see citing works
Force percolation of contractile active gels
Alvarado, J., Sheinman, M., Sharma, A., MacKintosh, F. C., & Koenderink, G. H. (2017) · Soft Matter · doi:10.1039/c7sm00834a · Cited by 78 · see citing works
Systematic construction and validation of an immune prognostic model for lung adenocarcinoma
Luo, C., Lei, M., Zhang, Y., Zhang, Q., Li, L., Lian, J., Liu, S., Wang, L., Pi, G., & Zhang, Y. (2019) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.14719 · Cited by 73 · see citing works
Anillin: a pivotal organizer of the cytokinetic machinery
Hickson, G. R. X., & O’Farrell, P. H. (2008) · Biochemical Society Transactions · doi:10.1042/bst0360439 · Cited by 76 · see citing works
Stabilization of the Actomyosin Ring Enables Spermatocyte Cytokinesis in Drosophila
Goldbach, P., Wong, R., Beise, N., Sarpal, R., Trimble, W. S., & Brill, J. A. (2010) · Molecular Biology of the Cell · doi:10.1091/mbc.e09-08-0714 · Cited by 74 · see citing works
The multifarious regulation of the apical junctional complex
Rusu, A. D., & Γεωργίου, Μ. (2020) · Open Biology · doi:10.1098/rsob.190278 · Cited by 71 · see citing works
Role of Anillin in Tumour: From a Prognostic Biomarker to a Novel Target
Nguyen, T. M., & Lee, C. H. (2020) · Cancers · doi:10.3390/cancers12061600 · Cited by 67 · see citing works
Goyal, A., Takaine, M., Simanis, V., & Nakano, K. (2011) · Cytoskeleton · doi:10.1002/cm.20500 · Cited by 67 · see citing works
Swanson, K. D., Lok, E., & Wong, E. T. (2016) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-015-0606-5 · Cited by 65 · see citing works
Germline cyst formation and incomplete cytokinesis during Drosophila melanogaster oogenesis
Ong, S., & Tan, C. L. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.10.018 · Cited by 66 · see citing works
Myosin IIA is involved in the endocytosis of CXCR4 induced by SDF-1α
Rey, M., Valenzuela-Fernández, A., Urzainqui, A., Yáñez‐Mó, M., Pérez‐Martínez, M., Penela, P., Mayor, F., & Sánchez‐Madrid, F. (2007) · Journal of Cell Science · doi:10.1242/jcs.03415 · Cited by 64 · see citing works
Vale, R. D., Spudich, J. A., & Griffis, E. R. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200902083 · Cited by 62 · see citing works
Small molecules discovered in a pathway screen target the Rho pathway in cytokinesis
Castoreno, A. B., Smurnyy, Y. D., Torres, A. D., Vokes, M. S., Jones, T. R., Carpenter, A. E., & Eggert, U. (2010) · Nature Chemical Biology · doi:10.1038/nchembio.363 · Cited by 61 · see citing works
Leone, M., Musa, G., & Engel, F. B. (2018) · Cardiovascular Research · doi:10.1093/cvr/cvy056 · Cited by 62 · see citing works
Prognostic significance of ANLN in lung adenocarcinoma
Long, X., Zhou, W., Wang, Y., & Liu, S. (2018) · Oncology Letters · doi:10.3892/ol.2018.8858 · Cited by 62 · see citing works
Cross-linkers both drive and brake cytoskeletal remodeling and furrowing in cytokinesis
Descovich, C. P., Cortes, D. B., Ryan, S., Nash, J., Zhang, L., Maddox, P. S., Nédélec, F., & Maddox, A. S. (2017) · Molecular Biology of the Cell · doi:10.1091/mbc.e17-06-0392 · Cited by 61 · see citing works
Wang, Y. (2005) · Trends in Cell Biology · doi:10.1016/j.tcb.2005.09.006 · Cited by 61 · see citing works
Myosin II isoform co-assembly and differential regulation in mammalian systems
Beach, J. R., & Hammer, J. A. (2015) · Experimental Cell Research · doi:10.1016/j.yexcr.2015.01.012 · Cited by 58 · see citing works
Wang, D., Chadha, G., Feygin, A., & Ivanov, A. I. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-1890-6 · Cited by 58 · see citing works
Precise Tuning of Cortical Contractility Regulates Cell Shape during Cytokinesis
Taneja, N., Bersi, M. R., Baillargeon, S. M., Fenix, A. M., Cooper, J. A., Ohi, R., Gama, V., Merryman, W. D., & Burnette, D. T. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.03.041 · Cited by 60 · see citing works
MELK: a potential novel therapeutic target for TNBC and other aggressive malignancies
Pitner, M. K., Taliaferro, J. M., Dalby, K. N., & Bartholomeusz, C. (2017) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2017.1363183 · Cited by 59 · see citing works
Cytokinesis and the contractile ring in fission yeast: towards a systems-level understanding
Bathe, M., & Chang, F. (2009) · Trends in Microbiology · doi:10.1016/j.tim.2009.10.002 · Cited by 58 · see citing works
Protein Dynamics in Individual Human Cells: Experiment and Theory
Cohen, A. A., Tomer Kalisky, C., Mayo, A., Geva‐Zatorsky, N., Danon, T., Issaeva, I., Kopito, R. B., Perzov, N., Milo, R., Sigal, A., et al. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004901 · Cited by 57 · see citing works
Cortical PAR polarity proteins promote robust cytokinesis during asymmetric cell division
Jordan, S. N., Davies, T., Zhuravlev, Y., Dumont, J., Shirasu‐Hiza, M., & Canman, J. C. (2016) · The Journal of Cell Biology · doi:10.1083/jcb.201510063 · Cited by 57 · see citing works
Anillin propels myosin-independent constriction of actin rings
Kučera, O., Siahaan, V., Janda, D., Dijkstra, S., Pilátová, E., Žatecká, E., Diez, S., Braun, M., & Lánský, Z. (2021) · Nature Communications · doi:10.1038/s41467-021-24474-1 · Cited by 52 · see citing works
Gatt, M. K., & Glover, D. M. (2006) · Journal of Cell Science · doi:10.1242/jcs.02933 · Cited by 54 · see citing works
Non-muscle myosin 2 at a glance
Quintanilla, M. A., Hammer, J. A., & Beach, J. R. (2023) · Journal of Cell Science · doi:10.1242/jcs.260890 · Cited by 53 · see citing works
Page, Y. L., Chartrain, I., Badouel, C., & Tassan, J. (2011) · Journal of Cell Science · doi:10.1242/jcs.069567 · Cited by 53 · see citing works
Anillin promotes astral microtubule-directed cortical myosin polarization
Tse, Y. C., Piekny, A. J., & Glotzer, M. (2011) · Molecular Biology of the Cell · doi:10.1091/mbc.e11-05-0399 · Cited by 49 · see citing works
Centralspindlin in Rappaport’s cleavage signaling
Mishima, M. (2016) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2016.03.006 · Cited by 51 · see citing works
Wang, D., Naydenov, N. G., Dozmorov, M. G., Koblinski, J. E., & Ivanov, A. I. (2020) · Breast Cancer Research · doi:10.1186/s13058-019-1241-x · Cited by 53 · see citing works
- Authors
- Straight, A. F., Field, C. M., & Mitchison, T. J.
- Affiliations
- Stanford Medicine (US)
- Harvard University (US)
- Venue
- Molecular Biology of the Cell
- Published
- 2005-01
- Volume
- 16
- Issue
- 1
- Pages
- 193-201
- ISSN
- 1059-1524 (ISSN-L)
- 1939-4586
- PMC
- PMC539163
- OpenAlex
- W2127504108
- Cited by
- 283
- References
- 41
- Citations by year
- 2026: 3 · 2025: 9 · 2024: 8 · 2023: 10 · 2022: 14 · 2021: 13 · 2020: 16 · 2019: 14 · 2018: 11 · 2017: 15 · 2016: 16 · 2015: 11 · 2014: 13 · 2013: 13 · 2012: 13
- FWCI
- 5.10
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Molecular Biology of the Cell (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Damon Runyon Cancer Research Foundation
- National Institute of General Medical Sciences (GM-023928, R01GM023928)
- 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
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Keywords
- anillin, non-muscle myosin II, contractile ring, cytokinesis, myosin light chain phosphorylation, abscission, cytokinesis failure, protein-protein interaction, Drosophila
- MeSH terms
- Amino Acid Sequence, Animals, Cell Line, Chromatography, Chromatography, Affinity, Cloning, Molecular, Contractile Proteins, Cytoskeleton, DNA, Drosophila, HeLa Cells, Humans, Interphase, Metaphase, Microscopy, Fluorescence, Molecular Sequence Data, Muscle Contraction, Myosins, Phosphorylation, Protein Binding, RNA, RNA, Double-Stranded, Xenopus laevis, Blotting, Western, Sequence Homology, Amino Acid, Myosin Type II, RNA Interference, Immunoprecipitation, Cytokinesis
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