J. H. Hurley, ESCRTs are everywhere, The EMBO Journal, vol.34, issue.19, pp.2398-2407, 2015.
DOI : 10.15252/embj.201592484

URL : http://embojnl.embopress.org/content/embojnl/34/19/2398.full.pdf

P. I. Hanson and A. Cashikar, Multivesicular Body Morphogenesis, Annual Review of Cell and Developmental Biology, vol.28, issue.1, pp.337-362, 2012.
DOI : 10.1146/annurev-cellbio-092910-154152

J. G. Carlton and J. Martin-serrano, Parallels Between Cytokinesis and Retroviral Budding: A Role for the ESCRT Machinery, Science, vol.133, issue.23, pp.1908-1912, 2007.
DOI : 10.1242/dev.02654

J. Guizetti, Cortical Constriction During Abscission Involves Helices of ESCRT-III-Dependent Filaments, Science, vol.17, issue.6, pp.1616-1620, 2011.
DOI : 10.1016/j.str.2009.04.007

N. Elia, R. Sougrat, T. A. Spurlin, J. H. Hurley, and J. Lippincott-schwartz, Dynamics of endosomal sorting complex required for transport (ESCRT) machinery during cytokinesis and its role in abscission, Proceedings of the National Academy of Sciences, vol.3568, issue.48, pp.4846-4851, 2011.
DOI : 10.1117/12.336833

J. Lafaurie-janvore, ESCRT-III Assembly and Cytokinetic Abscission Are Induced by Tension Release in the Intercellular Bridge, Science, vol.446, issue.7137, pp.1625-1629, 2013.
DOI : 10.1038/nature05722

B. Mierzwa and D. W. Gerlich, Cytokinetic Abscission: Molecular Mechanisms and Temporal Control, Developmental Cell, vol.31, issue.5, pp.525-538, 2014.
DOI : 10.1016/j.devcel.2014.11.006

URL : https://doi.org/10.1016/j.devcel.2014.11.006

M. Vietri, Spastin and ESCRT-III coordinate mitotic spindle disassembly and nuclear envelope sealing, Nature, vol.116, issue.7555, pp.231-235, 2015.
DOI : 10.1006/jsbi.1996.0013

Y. Olmos, L. Hodgson, J. Mantell, P. Verkade, and J. G. Carlton, ESCRT-III controls nuclear envelope reformation, Nature, vol.96, issue.7555, pp.236-239, 2015.
DOI : 10.1016/S0091-679X(10)96026-3

URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4471131/pdf

M. Raab, ESCRT III repairs nuclear envelope ruptures during cell migration to limit DNA damage and cell death, Science, vol.39, issue.19, pp.359-362, 2016.
DOI : 10.1038/sj.gt.3301292

C. M. Denais, Nuclear envelope rupture and repair during cancer cell migration, Science, vol.5, issue.4, pp.353-358, 2016.
DOI : 10.1038/ncomms6646

URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4833568/pdf

A. J. Jimenez, ESCRT Machinery Is Required for Plasma Membrane Repair, Science, vol.13, issue.1, p.1247136, 2014.
DOI : 10.1080/07391102.1995.10508818

U. K. Von-schwedler, The Protein Network of HIV Budding, Cell, vol.114, issue.6, pp.701-713, 2003.
DOI : 10.1016/S0092-8674(03)00714-1

M. Bleck, Temporal and spatial organization of ESCRT protein recruitment during HIV-1 budding, Proceedings of the National Academy of Sciences, vol.12, issue.1, pp.12211-12216, 2014.
DOI : 10.1016/j.micron.2005.03.014

M. F. Baietti, Syndecan???syntenin???ALIX regulates the biogenesis of exosomes, Nature Cell Biology, vol.264, issue.7, pp.677-685, 2012.
DOI : 10.1074/jbc.M106608200

K. Choudhuri, Polarized release of T-cell-receptor-enriched microvesicles at the immunological synapse, Nature, vol.14, issue.7490, pp.118-123, 2014.
DOI : 10.1017/S1431927608080306

T. Matusek, The ESCRT machinery regulates the secretion and long-range activity of Hedgehog, Nature, vol.516, issue.7529, pp.99-103, 2014.
DOI : 10.1073/pnas.93.9.4224

URL : https://hal.archives-ouvertes.fr/hal-01117493

W. M. Henne, H. Stenmark, and S. D. Emr, Molecular mechanisms of the membrane 399 sculpting ESCRT pathway, Cold Spring Harb Perspect Biol, vol.5, 2013.

J. Mccullough, L. A. Colf, and W. Sundquist, Membrane Fission Reactions of the Mammalian ESCRT Pathway, Annual Review of Biochemistry, vol.82, issue.1, pp.663-692, 2013.
DOI : 10.1146/annurev-biochem-072909-101058

S. Peel, P. Macheboeuf, N. Martinelli, and W. Weissenhorn, Divergent pathways lead to ESCRT-III-catalyzed membrane fission, Trends in Biochemical Sciences, vol.36, issue.4, pp.199-210, 2011.
DOI : 10.1016/j.tibs.2010.09.004

J. H. Hurley and P. Hanson, Membrane budding and scission by the ESCRT machinery: it's all in the neck, Nature Reviews Molecular Cell Biology, vol.122, issue.8, pp.556-566, 2010.
DOI : 10.1091/mbc.E07-07-0694

J. Guizetti and D. W. Gerlich, ESCRT-III polymers in membrane neck constriction, Trends in Cell Biology, vol.22, issue.3, pp.133-140, 2012.
DOI : 10.1016/j.tcb.2011.11.007

O. Schmidt and D. Teis, The ESCRT machinery, Current Biology, vol.22, issue.4, pp.116-120, 2012.
DOI : 10.1016/j.cub.2012.01.028

URL : https://doi.org/10.1016/j.cub.2012.01.028

J. Schoneberg, I. H. Lee, J. H. Iwasa, and J. H. Hurley, Reverse-topology membrane scission by the ESCRT proteins, Nature Reviews Molecular Cell Biology, vol.4, issue.1, pp.5-17, 2017.
DOI : 10.1534/genetics.115.178939

L. Christ, C. Raiborg, E. M. Wenzel, C. Campsteijn, and H. Stenmark, Cellular Functions 412 and Molecular Mechanisms of the ESCRT Membrane-Scission Machinery, Trends Biochem, p.413

M. Babst, D. J. Katzmann, E. J. Estepa-sabal, T. Meerloo, and S. D. Emr, Escrt-III, Developmental Cell, vol.3, issue.2, pp.271-282, 2002.
DOI : 10.1016/S1534-5807(02)00220-4

URL : https://doi.org/10.1016/s1534-5807(02)00220-4

R. Y. Samson, T. Obita, S. M. Freund, R. L. Williams, and S. D. Bell, A Role for the ESCRT System in Cell Division in Archaea, Science, vol.80, issue.15, pp.1710-1713, 2008.
DOI : 10.1128/JVI.00522-06

D. Teis, S. Saksena, and S. D. Emr, Ordered Assembly of the ESCRT-III Complex on Endosomes Is Required to Sequester Cargo during MVB Formation, Developmental Cell, vol.15, issue.4, pp.578-589, 2008.
DOI : 10.1016/j.devcel.2008.08.013

D. Teis, S. Saksena, B. L. Judson, and S. D. Emr, ESCRT-II coordinates the assembly of 423 ESCRT-III filaments for cargo sorting and multivesicular body vesicle formation, EMBO J, vol.424, pp.29-871, 2010.

S. Saksena, J. Wahlman, D. Teis, A. E. Johnson, and S. D. Emr, Functional Reconstitution of ESCRT-III Assembly and Disassembly, Cell, vol.136, issue.1, pp.97-109, 2009.
DOI : 10.1016/j.cell.2008.11.013

URL : https://doi.org/10.1016/j.cell.2008.11.013

T. Wollert, C. Wunder, J. Lippincott-schwartz, and J. H. Hurley, Membrane scission by the ESCRT-III complex, Nature, vol.15, issue.7235, pp.172-177, 2009.
DOI : 10.1042/bj2320033

URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2743992/pdf

L. A. Carlson and J. H. Hurley, In vitro reconstitution of the ordered assembly of the 430 endosomal sorting complex required for transport at membrane-bound HIV-1 Gag clusters, p.431

M. Babst, B. Wendland, E. J. Estepa, and S. D. Emr, The Vps4p AAA ATPase regulates membrane association of a Vps protein complex required for normal endosome function, The EMBO Journal, vol.17, issue.11, pp.2982-2993, 1998.
DOI : 10.1093/emboj/17.11.2982

T. Obita, Structural basis for selective recognition of ESCRT-III by the AAA ATPase 436

M. D. Stuchell-brereton, ESCRT-III recognition by VPS4 ATPases, Nature, vol.8, issue.7163, pp.740-438, 2007.
DOI : 10.1038/nature06172

S. Lata, Helical Structures of ESCRT-III Are Disassembled by VPS4, Science, vol.374, issue.6518, pp.1354-1357, 2008.
DOI : 10.1038/374186a0

URL : https://hal.archives-ouvertes.fr/cea-00817064

M. A. Adell, Coordinated binding of Vps4 to ESCRT-III drives membrane neck constriction during MVB vesicle formation, The Journal of Cell Biology, vol.205, issue.1, pp.33-49, 2014.
DOI : 10.1083/jcb.201310114.dv

B. Yang, G. Stjepanovic, Q. Shen, A. Martin, and J. Hurley, Vps4 disassembles an 444 ESCRT-III filament by global unfolding and processive translocation, Nat Struct Mol Biol, vol.445, pp.22-492, 2015.
DOI : 10.1038/nsmb.3015

S. Ghazi-tabatabai, Structure and Disassembly of Filaments Formed by the ESCRT-III Subunit Vps24, Structure, vol.16, issue.9, pp.1345-1356, 2008.
DOI : 10.1016/j.str.2008.06.010

R. Pires, A Crescent-Shaped ALIX Dimer Targets ESCRT-III CHMP4 Filaments, Structure, vol.17, issue.6, pp.843-856, 2009.
DOI : 10.1016/j.str.2009.04.007

URL : https://hal.archives-ouvertes.fr/inserm-00405383

W. M. Henne, N. J. Buchkovich, Y. Zhao, and S. D. Emr, The Endosomal Sorting Complex ESCRT-II Mediates the Assembly and Architecture of ESCRT-III Helices, Cell, vol.151, issue.2, pp.356-452, 2012.
DOI : 10.1016/j.cell.2012.08.039

Q. T. Shen, Structural analysis and modeling reveals new mechanisms governing ESCRT-III spiral filament assembly, The Journal of Cell Biology, vol.5, issue.6, pp.763-777, 2014.
DOI : 10.1002/prot.23094

URL : http://jcb.rupress.org/content/jcb/206/6/763.full.pdf

N. Chiaruttini, Relaxation of Loaded ESCRT-III Spiral Springs Drives Membrane Deformation, Cell, vol.163, issue.4, pp.866-879, 2015.
DOI : 10.1016/j.cell.2015.10.017

URL : https://hal.archives-ouvertes.fr/hal-01238262

J. Mccullough, Structure and membrane remodeling activity of ESCRT-III helical polymers, Science, vol.1, issue.1, pp.1548-1551, 2015.
DOI : 10.1034/j.1600-0854.2000.010106.x

B. J. Mcmillan, Electrostatic Interactions between Elongated Monomers Drive Filamentation of Drosophila Shrub, a Metazoan ESCRT-III Protein, Cell Reports, vol.16, issue.5, pp.1211-1217, 2016.
DOI : 10.1016/j.celrep.2016.06.093

P. I. Hanson, R. Roth, Y. Lin, and J. Heuser, Plasma membrane deformation by circular arrays of ESCRT-III protein filaments, The Journal of Cell Biology, vol.2, issue.2, pp.389-402, 2008.
DOI : 10.1073/pnas.0603788103

A. G. Cashikar, Structure of cellular ESCRT-III spirals and their relationship to HIV 465 budding, Elife, vol.3, 2014.
DOI : 10.7554/elife.02184

URL : https://cdn.elifesciences.org/articles/02184/elife-02184-v2.pdf

M. Babst, T. K. Sato, L. M. Banta, and S. D. Emr, Endosomal transport function in yeast requires a novel AAA-type ATPase, Vps4p, The EMBO Journal, vol.16, issue.8, pp.1820-1831, 1997.
DOI : 10.1093/emboj/16.8.1820

URL : http://emboj.embopress.org/content/embojnl/16/8/1820.full.pdf

I. H. Lee, H. Kai, L. A. Carlson, J. T. Groves, and J. H. Hurley, Negative membrane curvature catalyzes nucleation of endosomal sorting complex required for transport (ESCRT)-III assembly, Proceedings of the National Academy of Sciences, vol.3, issue.6, pp.15892-15897, 2015.
DOI : 10.1371/journal.pcbi.1000575

A. G. Cashikar, Structure of cellular ESCRT-III spirals and their relationship to HIV 472 budding, Elife, p.2184, 2014.

A. Roll-mecak and R. D. Vale, Structural basis of microtubule severing by the hereditary spastic paraplegia protein spastin, Nature, vol.303, issue.7176, pp.363-367, 2008.
DOI : 10.1038/nature06482

N. Elia, G. Fabrikant, M. M. Kozlov, and J. Lippincott-schwartz, Computational model of 476 cytokinetic abscission driven by ESCRT-III polymerization and remodeling, Biophys J, vol.102, pp.477-2309, 2012.

S. L. Kline-smith and C. Walczak, Mitotic Spindle Assembly and Chromosome Segregation, Molecular Cell, vol.15, issue.3, pp.317-327, 2004.
DOI : 10.1016/j.molcel.2004.07.012

URL : https://doi.org/10.1016/j.molcel.2004.07.012

T. D. Pollard, L. Blanchoin, and R. D. Mullins, Molecular Mechanisms Controlling Actin Filament Dynamics in Nonmuscle Cells, Annual Review of Biophysics and Biomolecular Structure, vol.29, issue.1, pp.545-576, 2000.
DOI : 10.1146/annurev.biophys.29.1.545

I. Zemp, Distinct cytoplasmic maturation steps of 40S ribosomal subunit precursors require hRio2, The Journal of Cell Biology, vol.248, issue.7, pp.1167-1180, 2009.
DOI : 10.1083/jcb.200904048.dv

URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2712965/pdf

I. Poser, BAC TransgeneOmics: a high-throughput method for exploration of protein function in mammals, Nature Methods, vol.179, issue.5, pp.409-415, 2008.
DOI : 10.1038/nrm1979

M. Y. Hein, A Human Interactome in Three Quantitative Dimensions Organized by Stoichiometries and Abundances, Cell, vol.163, issue.3, pp.712-723, 2015.
DOI : 10.1016/j.cell.2015.09.053

URL : https://doi.org/10.1016/j.cell.2015.09.053

M. H. Schmitz and D. W. Gerlich, Automated Live Microscopy to Study Mitotic Gene Function in Fluorescent Reporter Cell Lines, Methods Mol Biol, vol.545, pp.113-134, 2009.
DOI : 10.1007/978-1-60327-993-2_7

G. Lukinavicius, Fluorogenic probes for live-cell imaging of the cytoskeleton, Nature Methods, vol.260, issue.7, pp.731-733, 2014.
DOI : 10.1038/nmeth.2019

J. Schindelin, Fiji: an open-source platform for biological-image analysis, Nature Methods, vol.27, issue.7, pp.676-682, 2012.
DOI : 10.1093/bioinformatics/btr390

URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3855844/pdf