S. Brunet and M. Verlhac, Positioning to get out of meiosis: the asymmetry of division, Human Reproduction Update, vol.17, issue.1, pp.68-75, 2011.
DOI : 10.1093/humupd/dmq044

R. Li and D. Albertini, The road to maturation: somatic cell interaction and self-organization of the mammalian oocyte, Nature Reviews Molecular Cell Biology, vol.217, issue.3, pp.141-52, 2013.
DOI : 10.1095/biolreprod.109.082057

J. Azoury, K. Lee, V. Georget, P. Rassinier, B. Leader et al., Spindle Positioning in Mouse Oocytes Relies on a Dynamic Meshwork of Actin Filaments, Current Biology, vol.18, issue.19, pp.1514-1533, 2008.
DOI : 10.1016/j.cub.2008.08.044

M. Schuh and J. Ellenberg, A New Model for Asymmetric Spindle Positioning in Mouse Oocytes, Current Biology, vol.18, issue.24, pp.1986-92, 2008.
DOI : 10.1016/j.cub.2008.11.022

A. Chaigne, M. Verlhac, and M. Terret, Spindle positioning in mammalian oocytes, Experimental Cell Research, vol.318, issue.12, pp.1442-1449, 2012.
DOI : 10.1016/j.yexcr.2012.02.019

S. Connors, M. Kanatsu-shinohara, R. Schultz, and G. Kopf, Involvement of the Cytoskeleton in the Movement of Cortical Granules during Oocyte Maturation, and Cortical Granule Anchoring in Mouse Eggs, Developmental Biology, vol.200, issue.1, pp.103-118, 1998.
DOI : 10.1006/dbio.1998.8945

F. Longo and D. Chen, Development of cortical polarity in mouse eggs: Involvement of the meiotic apparatus, Developmental Biology, vol.107, issue.2, pp.382-94, 1985.
DOI : 10.1016/0012-1606(85)90320-3

B. Maro, M. Johnson, M. Webb, and G. Flach, Mechanism of polar body formation in the mouse oocyte: an interaction between the chromosomes, the cytoskeleton and the plasma membrane, J Embryol Exp Morphol, vol.92, pp.11-32, 1986.

J. Van-blerkom and H. Bell, Regulation of development in the fully grown mouse oocyte: chromosomemediated temporal and spatial differentiation of the cytoplasm and plasma membrane, J Embryol Exp Morphol, vol.93, pp.213-251, 1986.

M. Deng, P. Suraneni, R. Schultz, and R. Li, The Ran GTPase Mediates Chromatin Signaling to??Control Cortical Polarity during Polar Body Extrusion in Mouse Oocytes, Developmental Cell, vol.12, issue.2, pp.301-309, 2007.
DOI : 10.1016/j.devcel.2006.11.008

J. Dumont, S. Petri, F. Pellegrin, M. Terret, M. Bohnsack et al., A centriole- and RanGTP-independent spindle assembly pathway in meiosis I of vertebrate oocytes, The Journal of Cell Biology, vol.112, issue.3, pp.295-305, 2007.
DOI : 10.1146/annurev.cellbio.20.012103.094648

Y. Hao and I. Macara, Regulation of chromatin binding by a conformational switch in the tail of the Ran exchange factor RCC1, The Journal of Cell Biology, vol.112, issue.5, pp.827-863, 2008.
DOI : 10.1126/science.288.5470.1429

K. Yi, J. Unruh, M. Deng, B. Slaughter, B. Rubinstein et al., Dynamic maintenance of asymmetric meiotic spindle position through Arp2/3-complex-driven cytoplasmic streaming in mouse oocytes, Nature Cell Biology, vol.269, issue.10
DOI : 10.1016/j.jsb.2005.06.002

K. Yi and R. Li, Actin cytoskeleton in cell polarity and asymmetric division during mouse oocyte maturation, Cytoskeleton, vol.68, issue.3, pp.727-764, 2012.
DOI : 10.1002/cm.21048

K. Yi, B. Rubinstein, J. Unruh, F. Guo, B. Slaughter et al., Sequential actin-based pushing forces drive meiosis I chromosome migration and symmetry breaking in oocytes, The Journal of Cell Biology, vol.109, issue.5, pp.567-76, 2013.
DOI : 10.1126/science.1219147

B. Dehapiot, V. Carrière, J. Carroll, and G. Halet, Polarized Cdc42 activation promotes polar body protrusion and asymmetric division in mouse oocytes, Developmental Biology, vol.377, issue.1, pp.202-212, 2013.
DOI : 10.1016/j.ydbio.2013.01.029
URL : https://hal.archives-ouvertes.fr/inserm-00824856

J. Condeelis, Life at the Leading Edge: The Formation of Cell Protrusions, Annual Review of Cell Biology, vol.9, issue.1, pp.411-455, 1993.
DOI : 10.1146/annurev.cb.09.110193.002211

T. Pollard and G. Borisy, Cellular Motility Driven by Assembly and Disassembly of Actin Filaments, Cell, vol.112, issue.4, pp.453-465, 2003.
DOI : 10.1016/S0092-8674(03)00120-X

G. Halet and J. Carroll, Rac Activity Is Polarized and Regulates Meiotic Spindle Stability and Anchoring in Mammalian Oocytes, Developmental Cell, vol.12, issue.2, pp.309-326, 2007.
DOI : 10.1016/j.devcel.2006.12.010

R. Yanagimachi, Chapter 4 Sperm-Egg Association in Mammals, Curr Top Dev Biol, vol.12, pp.83-105, 1978.
DOI : 10.1016/S0070-2153(08)60594-3

K. Runge, J. Evans, Z. He, S. Gupta, K. Mcdonald et al., Oocyte CD9 is enriched on the microvillar membrane and required for normal microvillar shape and distribution, Developmental Biology, vol.304, issue.1, pp.317-342, 2007.
DOI : 10.1016/j.ydbio.2006.12.041

A. Jégou, A. Ziyyat, V. Barraud-lange, E. Perez, J. Wolf et al., CD9 tetraspanin generates fusion competent sites on the egg membrane for mammalian fertilization, Proceedings of the National Academy of Sciences, vol.108, issue.27, pp.10946-51, 2011.
DOI : 10.1073/pnas.1017400108

J. Luo, L. Mcginnis, and W. Kinsey, Fyn kinase activity is required for normal organization and functional polarity of the mouse oocyte cortex, Molecular Reproduction and Development, vol.23, issue.9, pp.819-850, 2009.
DOI : 10.1002/mrd.21034

S. Yonemura, S. Tsukita, and S. Tsukita, Direct Involvement of Ezrin/Radixin/Moesin (ERM)-binding Membrane Proteins in the Organization of Microvilli in Collaboration with Activated ERM Proteins, The Journal of Cell Biology, vol.108, issue.7, pp.1497-1509, 1999.
DOI : 10.1073/pnas.94.7.3010

R. Fehon, A. Mcclatchey, and A. Bretscher, Organizing the cell cortex: the role of ERM proteins, Nature Reviews Molecular Cell Biology, vol.18, issue.4, pp.276-87, 2010.
DOI : 10.1038/nrm2866

B. Fievet, A. Gautreau, C. Roy, D. Maestro, L. Mangeat et al., Phosphoinositide binding and phosphorylation act sequentially in the activation mechanism of ezrin, The Journal of Cell Biology, vol.115, issue.5, pp.653-662, 2004.
DOI : 10.1083/jcb.145.7.1497

S. Louvet, J. Aghion, A. Santa-maria, P. Mangeat, and B. Maro, Ezrin Becomes Restricted to Outer Cells Following Asymmetrical Division in the Preimplantation Mouse Embryo, Developmental Biology, vol.177, issue.2, pp.568-79, 1996.
DOI : 10.1006/dbio.1996.0186

S. Larson, H. Lee, P. Hung, L. Matthews, D. Robinson et al., Cortical Mechanics and Meiosis II Completion in Mammalian Oocytes Are Mediated by Myosin-II and Ezrin-Radixin-Moesin (ERM) Proteins, Molecular Biology of the Cell, vol.21, issue.18, pp.3182-92, 2010.
DOI : 10.1091/mbc.E10-01-0066

M. Brown, R. Nijhara, J. Hallam, M. Gignac, K. Yamada et al., Chemokine stimulation of human peripheral blood T lymphocytes induces rapid dephosphorylation of ERM proteins, which facilitates loss of microvilli and polarization, Blood, vol.102, issue.12, pp.3890-99, 2003.
DOI : 10.1182/blood-2002-12-3807

J. Chen, J. Cohn, and L. Mandel, Dephosphorylation of ezrin as an early event in renal microvillar breakdown and anoxic injury., Proceedings of the National Academy of Sciences, vol.92, issue.16, pp.7495-7504, 1995.
DOI : 10.1073/pnas.92.16.7495

T. Kondo, K. Takeuchi, Y. Doi, S. Yonemura, S. Nagata et al., ERM (Ezrin/Radixin/Moesin)-based Molecular Mechanism of Microvillar Breakdown at an Early Stage of Apoptosis, The Journal of Cell Biology, vol.256, issue.3, pp.749-58, 1997.
DOI : 10.1083/jcb.120.2.437

R. Nijhara, P. Van-hennik, M. Gignac, M. Kruhlak, P. Hordijk et al., Rac1 Mediates Collapse of Microvilli on Chemokine-Activated T Lymphocytes, The Journal of Immunology, vol.173, issue.8, pp.4985-93, 2004.
DOI : 10.4049/jimmunol.173.8.4985

S. Faure, L. Salazar-fontana, M. Semichon, V. Tybulewicz, G. Bismuth et al., ERM proteins regulate cytoskeleton relaxation promoting T cell???APC conjugation, Nature Immunology, vol.7, issue.3, pp.272-279, 2004.
DOI : 10.1038/ni1039

J. Rossy, M. Gutjahr, N. Blaser, D. Schlicht, and V. Niggli, Ezrin/moesin in motile Walker 256 carcinosarcoma cells: Signal-dependent relocalization and role in migration, Experimental Cell Research, vol.313, issue.6, pp.1106-1120, 2007.
DOI : 10.1016/j.yexcr.2006.12.023

E. Cernuda-morollón, J. Millán, M. Shipman, F. Marelli-berg, and A. Ridley, Rac Activation by the T-Cell Receptor Inhibits T Cell Migration, PLoS ONE, vol.117, issue.8, p.12393, 2010.
DOI : 10.1371/journal.pone.0012393.s009

J. Hao, Y. Liu, M. Kruhlak, K. Debell, B. Rellahan et al., Phospholipase C???mediated hydrolysis of PIP2 releases ERM proteins from lymphocyte membrane, The Journal of Cell Biology, vol.115, issue.3, pp.451-62, 2009.
DOI : 10.1038/sj.onc.1207768

G. Halet, R. Tunwell, T. Balla, K. Swann, and J. Carroll, The dynamics of plasma membrane PtdIns(4,5)P 2 at fertilization of mouse eggs, J Cell Sci, vol.115, pp.2139-2188, 2002.

C. Roubinet, B. Decelle, G. Chicanne, J. Dorn, B. Payrastre et al., Molecular networks linked by Moesin drive remodeling of the cell cortex during mitosis, The Journal of Cell Biology, vol.273, issue.1, pp.99-112, 2011.
DOI : 10.1101/gad.1785209

K. Takahashi, T. Sasaki, A. Mammoto, K. Takaishi, T. Kameyama et al., Direct Interaction of the Rho GDP Dissociation Inhibitor with Ezrin/Radixin/Moesin Initiates the Activation of the Rho Small G Protein, Journal of Biological Chemistry, vol.272, issue.37, pp.23371-23376, 1997.
DOI : 10.1074/jbc.272.37.23371

K. Hamada, A. Seto, T. Shimizu, T. Matsui, Y. Takai et al., Crystallization and preliminary crystallographic studies of RhoGDI in complex with the radixin FERM domain, Acta Crystallographica Section D Biological Crystallography, vol.57, issue.6, pp.889-90, 2001.
DOI : 10.1107/S090744490100556X

E. Sander, J. Klooster, S. Van-delft, R. Van-der-kammen, and J. Collard, Rac Downregulates Rho Activity, The Journal of Cell Biology, vol.11, issue.5, pp.1009-1030, 1999.
DOI : 10.1091/mbc.8.11.2329

S. Etienne-manneville and A. Hall, Rho GTPases in cell biology, Nature, vol.92, issue.6916, pp.629-664, 2002.
DOI : 10.1074/jbc.M108297200

E. Vaughan, A. Miller, H. Yu, and W. Bement, Control of Local Rho GTPase Crosstalk by Abr, Current Biology, vol.21, issue.4, pp.270-277, 2011.
DOI : 10.1016/j.cub.2011.01.014

F. Valderrama, S. Thevapala, and A. Ridley, Radixin regulates cell migration and cell-cell adhesion through Rac1, Journal of Cell Science, vol.125, issue.14, pp.3310-3329, 2012.
DOI : 10.1242/jcs.094383

D. Raucher and M. Sheetz, Cell Spreading and Lamellipodial Extension Rate Is Regulated by Membrane Tension, The Journal of Cell Biology, vol.108, issue.1, pp.127-163, 2000.
DOI : 10.1126/science.281.5373.105