J. C. Kasemeier-kulesa, P. M. Kulesa, and F. Lefcort, Imaging neural crest cell dynamics during formation of dorsal root ganglia and sympathetic ganglia, Development, vol.132, issue.2, pp.235-245, 2005.
DOI : 10.1242/dev.01553

M. A. Breau and S. Schneider-maunoury, Mechanisms of cranial placode assembly, The International Journal of Developmental Biology, vol.58, issue.1, pp.9-19, 2014.
DOI : 10.1387/ijdb.130351mb
URL : https://hal.archives-ouvertes.fr/hal-01538978

M. A. Breau and S. Schneider-maunoury, Cranial placodes: Models for exploring the multi-facets of cell adhesion in epithelial rearrangement, collective migration and neuronal movements, Developmental Biology, vol.401, issue.1, pp.25-36, 2015.
DOI : 10.1016/j.ydbio.2014.12.012
URL : https://hal.archives-ouvertes.fr/hal-01538973

A. Streit, The cranial sensory nervous system: specification of sensory progenitors and placodes, StemBook Cambridge Harvard Stem Cell Institute, 2008.
DOI : 10.3824/stembook.1.31.1

G. Schlosser, Making Senses, Int. Rev. Cell. Mol. Biol, vol.283, pp.129-234, 2010.
DOI : 10.1016/S1937-6448(10)83004-7

R. Aguillon, P. Blader, and J. Batut, Patterning, morphogenesis, and neurogenesis of zebrafish cranial sensory placodes, Methods Cell Biol, vol.134, pp.33-67, 2016.
DOI : 10.1016/bs.mcb.2016.01.002

T. Imai, Pre-Target Axon Sorting Establishes the Neural Map Topography, Science, vol.320, issue.5873, pp.585-590, 2009.
DOI : 10.1126/science.1153758

N. Miyasaka, H. Knaut, and Y. Yoshihara, Cxcl12/Cxcr4 chemokine signaling is required for placode assembly and sensory axon pathfinding in the zebrafish olfactory system, Development, vol.134, issue.13, pp.2459-2468, 2007.
DOI : 10.1242/dev.001958

C. E. Shiau, P. Y. Lwigale, R. M. Das, S. A. Wilson, and M. Bronner-fraser, Robo2-Slit1 dependent cell-cell interactions mediate assembly of the trigeminal ganglion, Nature Neuroscience, vol.212, issue.3, pp.269-276, 2008.
DOI : 10.1002/aja.1001940103

C. E. Shiau and M. Bronner-fraser, N-cadherin acts in concert with Slit1-Robo2 signaling in regulating aggregation of placode-derived cranial sensory neurons, Development, vol.136, issue.24, pp.4155-4164, 2009.
DOI : 10.1242/dev.034355

S. W. Lewellis, Precise SDF1-mediated cell guidance is achieved through ligand clearance and microRNA-mediated decay, The Journal of Cell Biology, vol.23, issue.Suppl, pp.337-355, 2013.
DOI : 10.1038/ng1251
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3563679

E. Theveneau, Chase-and-run between adjacent cell populations promotes directional collective migration, Nature Cell Biology, vol.36, issue.7, pp.1-12, 2013.
DOI : 10.1002/dvdy.21758
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4910871

H. Knaut, P. Blader, U. Strähle, and A. Schier, Assembly of Trigeminal Sensory Ganglia by Chemokine Signaling, Neuron, vol.47, issue.5, pp.653-666, 2005.
DOI : 10.1016/j.neuron.2005.07.014
URL : http://doi.org/10.1016/j.neuron.2005.07.014

N. Bhat and B. B. Riley, Integrin-??5 Coordinates Assembly of Posterior Cranial Placodes in Zebrafish and Enhances Fgf-Dependent Regulation of Otic/Epibranchial Cells, PLoS ONE, vol.6, issue.12, p.27778, 2011.
DOI : 10.1371/journal.pone.0027778.s009

A. Zecca, S. Dyballa, A. Voltes, R. Bradley, and C. Pujades, The Order and Place of Neuronal Differentiation Establish the Topography of Sensory Projections and the Entry Points within the Hindbrain, Journal of Neuroscience, vol.35, issue.19, pp.7475-7486, 2015.
DOI : 10.1523/JNEUROSCI.3743-14.2015

K. E. Whitlock and M. Westerfield, The olfactory placodes of the zebrafish form by convergence of cellular fields at the edge of the neural plate, Development, vol.127, pp.3645-3653, 2000.

K. E. Whitlock and M. Westerfield, A transient population of neurons pioneers the olfactory pathway in the zebrafish, J. Neurosci, vol.18, pp.8919-8927, 1998.

R. Madelaine, L. Garric, and P. Blader, Partially redundant proneural function reveals the importance of timing during zebrafish olfactory neurogenesis, Development, vol.138, issue.21, pp.4753-4762, 2011.
DOI : 10.1242/dev.066563

N. Miyasaka, Robo2 is required for establishment of a precise glomerular map in the zebrafish olfactory system, Development, vol.132, issue.6, pp.1283-1293, 2005.
DOI : 10.1242/dev.01698

V. Lakhina, Netrin/DCC Signaling Guides Olfactory Sensory Axons to Their Correct Location in the Olfactory Bulb, Journal of Neuroscience, vol.32, issue.13, pp.4440-4456, 2012.
DOI : 10.1523/JNEUROSCI.4442-11.2012

M. V. Harden, Close association of olfactory placode precursors and cranial neural crest cells does not predestine cell mixing, Developmental Dynamics, vol.132, issue.7, pp.1143-1154, 2012.
DOI : 10.1242/dev.02158
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4240535

|. Doi, 10.1038/s41467-017-00283-3 ARTICLE, NATURE COMMUNICATIONS NATURE COMMUNICATIONS |, vol.8
URL : https://hal.archives-ouvertes.fr/in2p3-00652853

J. Torres-paz and K. E. Whitlock, Olfactory sensory system develops from coordinated movements within the neural plate, Developmental Dynamics, vol.9, issue.12, pp.1619-1631, 2014.
DOI : 10.1016/j.gep.2009.04.001
URL : http://onlinelibrary.wiley.com/doi/10.1002/dvdy.24194/pdf

P. Blader, C. Plessy, and U. Strähle, Multiple regulatory elements with spatially and temporally distinct activities control neurogenin1 expression in primary neurons of the zebrafish embryo, Mechanisms of Development, vol.120, issue.2, pp.211-218, 2003.
DOI : 10.1016/S0925-4773(02)00413-6

D. J. Montell, Morphogenetic Cell Movements: Diversity from Modular Mechanical Properties, Science, vol.4, issue.9, pp.1502-1505, 2008.
DOI : 10.1038/ncb848

B. Monier and M. Suzanne, The Morphogenetic Role of Apoptosis, Curr. Top. Dev. Biol, vol.114, pp.335-362, 2015.
DOI : 10.1016/bs.ctdb.2015.07.027

L. Saias, Decrease in Cell Volume Generates Contractile Forces Driving Dorsal Closure, Developmental Cell, vol.33, issue.5, pp.611-621, 2015.
DOI : 10.1016/j.devcel.2015.03.016

F. Bosveld, Mechanical Control of Morphogenesis by Fat/Dachsous/Four-Jointed Planar Cell Polarity Pathway, Science, vol.27, issue.1, pp.724-727, 2012.
DOI : 10.1016/j.devcel.2010.11.007

O. Randlett, L. Poggi, F. R. Zolessi, and W. A. Harris, The Oriented Emergence of Axons from Retinal Ganglion Cells Is Directed by Laminin Contact In??Vivo, Neuron, vol.70, issue.2, pp.266-280, 2011.
DOI : 10.1016/j.neuron.2011.03.013

C. Jacobson, B. Schnapp, and G. A. Banker, A Change in the Selective Translocation of the Kinesin-1 Motor Domain Marks the Initial Specification of the Axon, Neuron, vol.49, issue.6, pp.797-804, 2006.
DOI : 10.1016/j.neuron.2006.02.005

J. L. Goldberg, How does an axon grow? Genes Dev, pp.941-958, 2003.
DOI : 10.1101/gad.1062303

F. Polleux and W. Snider, Initiating and Growing an Axon, Cold Spring Harbor Perspectives in Biology, vol.2, issue.4, p.1925, 2010.
DOI : 10.1101/cshperspect.a001925
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2845204

C. Norden, S. Young, B. A. Link, and W. A. Harris, Actomyosin Is the Main Driver of Interkinetic Nuclear Migration in the Retina, Cell, vol.138, issue.6, pp.1195-1208, 2009.
DOI : 10.1016/j.cell.2009.06.032

A. J. Ridley, Rho GTPase signalling in cell migration, Current Opinion in Cell Biology, vol.36, pp.103-112, 2015.
DOI : 10.1016/j.ceb.2015.08.005
URL : http://doi.org/10.1016/j.ceb.2015.08.005

Y. J. Liu, Confinement and Low Adhesion Induce Fast Amoeboid Migration of Slow Mesenchymal Cells, Cell, vol.160, issue.4, pp.659-672, 2015.
DOI : 10.1016/j.cell.2015.01.007

A. Ratheesh, R. Priya, and A. S. Yap, Coordinating Rho and Rac, Prog. Mol. Biol. Transl. Sci, vol.116, pp.49-68, 2013.
DOI : 10.1016/B978-0-12-394311-8.00003-0

F. Guilak, Compression-induced changes in the shape and volume of the chondrocyte nucleus, Journal of Biomechanics, vol.28, issue.12, pp.1529-1541, 1995.
DOI : 10.1016/0021-9290(95)00100-X

R. P. Martins, J. D. Finan, F. Guilak, and D. A. Lee, Mechanical Regulation of Nuclear Structure and Function, Annual Review of Biomedical Engineering, vol.14, issue.1, pp.431-455, 2012.
DOI : 10.1146/annurev-bioeng-071910-124638

M. Versaevel, T. Grevesse, and S. Gabriele, Spatial coordination between cell and nuclear shape within micropatterned endothelial cells, Nature Communications, vol.18, p.671, 2012.
DOI : 10.1080/07391102.2001.10506686

E. Panousopoulou and J. B. Green, Invagination of Ectodermal Placodes Is Driven by Cell Intercalation-Mediated Contraction of the Suprabasal Tissue Canopy, PLOS Biology, vol.188, issue.1, p.1002405, 2016.
DOI : 10.1371/journal.pbio.1002405.s011

M. Rauzi, P. Verant, T. Lecuit, and P. Lenne, Nature and anisotropy of cortical forces orienting Drosophila tissue morphogenesis, Nature Cell Biology, vol.420, issue.12, pp.1401-1410, 2008.
DOI : 10.1529/biophysj.105.071506
URL : https://hal.archives-ouvertes.fr/hal-00428938

M. Rauzi, P. F. Lenne, and T. Lecuit, Planar polarized actomyosin contractile flows control epithelial junction remodelling, Nature, vol.420, issue.7327, pp.1110-1114, 2010.
DOI : 10.1038/nature09566

K. Sugimura, P. F. Lenne, and F. Graner, Measuring forces and stresses in situ in living tissues, Development, vol.143, issue.2, pp.186-196, 2016.
DOI : 10.1242/dev.119776
URL : https://hal.archives-ouvertes.fr/hal-01445876

C. Collinet, M. Rauzi, P. F. Lenne, and T. Lecuit, Local and tissue-scale forces drive oriented junction growth during tissue extension, Nature Cell Biology, vol.420, issue.10, pp.1247-1258, 2015.
DOI : 10.1109/83.650848
URL : https://hal.archives-ouvertes.fr/hal-01428973

C. M. Lye, Mechanical Coupling between Endoderm Invagination and Axis Extension in Drosophila, PLOS Biology, vol.133, issue.23, p.1002292, 2015.
DOI : 10.1371/journal.pbio.1002292.s021
URL : http://doi.org/10.1371/journal.pbio.1002292

K. Boric, P. Orio, T. Viéville, and K. Whitlock, Quantitative Analysis of Cell Migration Using Optical Flow, PLoS ONE, vol.48, issue.7, p.69574, 2013.
DOI : 10.1371/journal.pone.0069574.s003
URL : https://hal.archives-ouvertes.fr/hal-00850523

K. M. Kwan, A complex choreography of cell movements shapes the vertebrate eye, Development, vol.139, issue.2, pp.359-372, 2012.
DOI : 10.1242/dev.071407

M. G. Heiman and S. Shaham, DEX-1 and DYF-7 Establish Sensory Dendrite Length by Anchoring Dendritic Tips during Cell Migration, Cell, vol.137, issue.2, pp.344-355, 2009.
DOI : 10.1016/j.cell.2009.01.057
URL : http://doi.org/10.1016/j.cell.2009.01.057

H. Simon and A. Lumsden, Rhombomere-specific origin of the contralateral vestibulo-acoustic efferent neurons and their migration across the embryonic midline, Neuron, vol.11, issue.2, pp.209-220, 1993.
DOI : 10.1016/0896-6273(93)90179-U

K. Kawaji, H. Umeshima, M. Eiraku, T. Hirano, and M. Kengaku, Dual phases of migration of cerebellar granule cells guided by axonal and dendritic leading processes, Molecular and Cellular Neuroscience, vol.25, issue.2, pp.228-240, 2004.
DOI : 10.1016/j.mcn.2003.10.006

Y. Hatanaka, Y. Zhu, M. Torigoe, Y. Kita, and F. Murakami, From migration to settlement: the pathways, migration modes and dynamics of neurons in the developing brain, Proceedings of the Japan Academy, Series B, vol.92, issue.1, pp.1-19, 2016.
DOI : 10.2183/pjab.92.1

F. Auclair, N. Valdés, and R. Marchand, Rhombomere-specific origin of branchial and visceral motoneurons of the facial nerve in the rat embryo, The Journal of Comparative Neurology, vol.120, issue.3, pp.451-461, 1996.
DOI : 10.1113/expphysiol.1913.sp000132

H. Wada, Dual roles of zygotic and maternal Scribble1 in neural migration and convergent extension movements in zebrafish embryos, Development, vol.132, issue.10, pp.2273-2285, 2005.
DOI : 10.1242/dev.01810

K. Franze, The mechanical control of nervous system development, Development, vol.140, issue.15, pp.3069-3077, 2013.
DOI : 10.1242/dev.079145

P. Weiss, NERVE PATTERNS: THE MECHANICS OF NERVE GROWTH, Third Growth Symposium, vol.5, pp.163-203, 1941.
DOI : 10.1016/B978-1-4832-2919-5.50026-X

J. R. Loverde and B. J. Pfister, Developmental axon stretch stimulates neuron growth while maintaining normal electrical activity, intracellular calcium flux, and somatic morphology, Frontiers in Cellular Neuroscience, vol.11, p.308, 2015.
DOI : 10.2174/1567202043480134
URL : http://doi.org/10.3389/fncel.2015.00308

M. Behrndt, Forces Driving Epithelial Spreading in Zebrafish Gastrulation, Science, vol.25, issue.11, pp.257-260, 2012.
DOI : 10.1093/bioinformatics/btp184

S. G. Megason, In Toto Imaging of Embryogenesis with Confocal Time-Lapse Microscopy, Methods Mol. Biol, vol.546, pp.317-332, 2009.
DOI : 10.1007/978-1-60327-977-2_19

E. Tahinci and K. Symes, Distinct functions of Rho and Rac are required for convergent extension during Xenopus gastrulation, Developmental Biology, vol.259, issue.2, pp.318-335, 2003.
DOI : 10.1016/S0012-1606(03)00206-9

D. J. Kozlowski, T. Murakami, R. K. Ho, and E. S. Weinberg, Regional cell movement and tissue patterning in the zebrafish embryo revealed by fate mapping with caged fluorescein, Biochemistry and Cell Biology, vol.75, issue.5, pp.551-562, 1997.
DOI : 10.1139/o97-090

N. Tarantino, TNF and IL-1 exhibit distinct ubiquitin requirements for inducing NEMO???IKK supramolecular structures, The Journal of Cell Biology, vol.19, issue.2, pp.231-245, 2014.
DOI : 10.1016/S1074-7613(00)80183-1
URL : https://hal.archives-ouvertes.fr/pasteur-01539965

R. Gorelik and A. Gautreau, Quantitative and unbiased analysis of directional persistence in cell migration, Nature Protocols, vol.504, issue.8, pp.1931-1943, 2014.
DOI : 10.1016/S0003-3472(83)80198-5

J. Ollion, J. Cochennec, F. Loll, C. Escudé, and T. Boudier, TANGO: a generic tool for high-throughput 3D image analysis for studying nuclear organization, Bioinformatics, vol.29, issue.14, pp.1840-1841, 2013.
DOI : 10.1093/bioinformatics/btt276
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3702251

S. Bolte and F. P. Cordelières, A guided tour into subcellular colocalization analysis in light microscopy, Journal of Microscopy, vol.56, issue.3, pp.213-232, 2006.
DOI : 10.1016/S0014-5793(03)00521-0
URL : https://hal.archives-ouvertes.fr/hal-00132481