D. Santo and J. , NATURAL KILLER CELL DEVELOPMENTAL PATHWAYS: A Question of Balance, Annual Review of Immunology, vol.24, issue.1
DOI : 10.1146/annurev.immunol.24.021605.090700

B. Blom and H. Spits, DEVELOPMENT OF HUMAN LYMPHOID CELLS, Annual Review of Immunology, vol.24, issue.1, pp.287-320, 2006.
DOI : 10.1146/annurev.immunol.24.021605.090612

N. Huntington, C. Vosshenrich, D. Santo, and J. , Developmental pathways that generate natural-killer-cell diversity in mice and humans, Nature Reviews Immunology, vol.109, issue.9, pp.703-714, 2007.
DOI : 10.1038/nri2154

M. Cherrier, C. Ohnmacht, S. Cording, and G. Eberl, Development and function of intestinal innate lymphoid cells, Current Opinion in Immunology, vol.24, issue.3, pp.277-283, 2012.
DOI : 10.1016/j.coi.2012.03.011
URL : https://hal.archives-ouvertes.fr/pasteur-01402726

M. Colonna, Interleukin-22-Producing Natural Killer Cells and Lymphoid Tissue Inducer-like Cells in Mucosal Immunity, Immunity, vol.31, issue.1, pp.15-23, 2009.
DOI : 10.1016/j.immuni.2009.06.008

S. Koyasu, K. Moro, M. Tanabe, and T. Takeuchi, Natural Helper Cells, Adv. Immunol, vol.108, pp.21-44, 2010.
DOI : 10.1016/B978-0-12-380995-7.00002-1

H. Spits, D. Santo, and J. , The expanding family of innate lymphoid cells: regulators and effectors of immunity and tissue remodeling, Nature Immunology, vol.169, issue.1, pp.21-27, 2011.
DOI : 10.1016/j.molimm.2004.06.010

@. Spits, H. Artis, D. Colonna, M. Diefenbach, A. et al., Innate lymphoid cells ??? a proposal for uniform nomenclature, Nature Reviews Immunology, vol.37, issue.2, pp.145-149, 2013.
DOI : 10.1038/nri3365

M. Kondo, I. Weissman, and K. Akashi, Identification of Clonogenic Common Lymphoid Progenitors in Mouse Bone Marrow, Cell, vol.91, issue.5, pp.661-72, 1997.
DOI : 10.1016/S0092-8674(00)80453-5

@. Wong, S. Walker, J. Jolin, H. Drynan, L. Hams et al., Transcription factor ROR?? is critical for nuocyte development, Nature Immunology, vol.173, issue.3, pp.229-236, 2012.
DOI : 10.1016/0092-8674(92)90029-C
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3343633

@. See-also, Q. Yang, S. Saenz, D. Zlotoff, D. Artis et al., Cutting edge: Natural helper cells derive from lymphoid progenitors, J. Immunol, vol.187, pp.5505-5509, 2011.

E. Rosmaraki, I. Douagi, C. Roth, F. Colucci, A. Cumano et al., Identification of committed NK cell progenitors in adult murine bone marrow, European Journal of Immunology, vol.30, issue.6, pp.1900-1909, 2001.
DOI : 10.1002/1521-4141(200106)31:6<1900::AID-IMMU1900>3.0.CO;2-M

@. Fathman, J. Bhattacharya, D. Inlay, M. Seita, J. Karsunky et al., Identification of the Earliest Committed Natural Killer Cell Progenitor in Murine Bone Marrow, Clinical Immunology, vol.135, pp.5439-5447, 2011.
DOI : 10.1016/j.clim.2010.03.401

@. See-also, C. Vosshenrich, T. Ranson, S. Samson, E. Corcuff et al., Roles for common cytokine receptor gamma-chain-dependent cytokines in the generation, differentiation, and maturation of NK cell precursors and peripheral NK cells in vivo, J. Immunol, vol.174, pp.1213-1221, 2005.

@. Ramirez, K. Chandler, K. Spaulding, C. Zandi, S. Sigvardsson et al., Gene Deregulation and Chronic Activation in Natural Killer Cells Deficient in the Transcription Factor ETS1, Immunity, vol.36, issue.6, pp.921-932, 2012.
DOI : 10.1016/j.immuni.2012.04.006

S. Carotta, S. Pang, S. Nutt, and G. Belz, Identification of the earliest NK-cell precursor in the mouse BM, Blood, vol.117, issue.20, pp.5449-5452, 2011.
DOI : 10.1182/blood-2010-11-318956

T. Halim, A. Maclaren, M. Romanish, M. Gold, K. Mcnagny et al., Retinoic-Acid-Receptor-Related Orphan Nuclear Receptor Alpha Is Required for Natural Helper Cell Development and Allergic Inflammation, Immunity, vol.37, issue.3, pp.463-474, 2012.
DOI : 10.1016/j.immuni.2012.06.012
URL : http://doi.org/10.1016/j.immuni.2012.06.012

S. Heinz and C. Glass, Roles of Lineage-Determining Transcription Factors in Establishing Open Chromatin: Lessons From High-Throughput Studies, Curr. Top. Microbiol. Immunol, vol.356, pp.1-15, 2012.
DOI : 10.1007/82_2011_142

K. Cui, C. Zang, T. Roh, D. Schones, R. Childs et al., Chromatin Signatures in Multipotent Human Hematopoietic Stem Cells Indicate the Fate of Bivalent Genes during Differentiation, Cell Stem Cell, vol.4, issue.1, pp.80-93, 2009.
DOI : 10.1016/j.stem.2008.11.011

H. Weishaupt, M. Sigvardsson, and J. Attema, Epigenetic chromatin states uniquely define the developmental plasticity of murine hematopoietic stem cells, Blood, vol.115, issue.2, p.247, 2010.
DOI : 10.1182/blood-2009-07-235176

@. Zhang, J. Mortazavi, A. Williams, B. Wold, B. Rothenberg et al., Dynamic Transformations of Genome-wide Epigenetic Marking and Transcriptional Control Establish T Cell Identity, Cell, vol.149, issue.2, pp.467-482, 2012.
DOI : 10.1016/j.cell.2012.01.056

Y. Yokota, A. Mansouri, S. Mori, S. Sugawara, S. Adachi et al., Identification of critical binding sites for Gata3 in early T cell progenitors that may control T lineage specification 23 Development of peripheral lymphoid organs and natural killer cells depends on the helix-loop-helix inhibitor Id2 Mature natural killer cell and lymphoid tissue-inducing cell development requires Id2-mediated suppression of E protein activity, Nature J. Exp. Med, vol.397, issue.204, pp.702-708, 1999.

P. Aliahmad, B. De-la-torre, and J. Kaye, Shared dependence on the DNA-binding factor TOX for the development of lymphoid tissue???inducer cell and NK cell lineages, Nature Immunology, vol.308, issue.10, pp.945-952, 2010.
DOI : 10.1038/sj.gt.3301206

J. Wang, A. Nichogiannopoulou, L. Wu, L. Sun, A. Sharpe et al., Selective Defects in the Development of the Fetal and Adult Lymphoid System in Mice with an Ikaros Null Mutation, Immunity, vol.5, issue.6, pp.537-586, 1996.
DOI : 10.1016/S1074-7613(00)80269-1

H. Zeng, R. Yücel, C. Kosan, L. Klein-hitpass, and T. Möröy, Transcription factor Gfi1 regulates self-renewal and engraftment of hematopoietic stem cells, The EMBO Journal, vol.16, issue.20, pp.4116-4125, 2004.
DOI : 10.1016/S1074-7613(02)00317-5

S. Dias, R. Månsson, S. Gurbuxani, M. Sigvardsson, and B. Kee, E2A Proteins Promote Development of Lymphoid-Primed Multipotent Progenitors, Immunity, vol.29, issue.2, pp.217-227, 2008.
DOI : 10.1016/j.immuni.2008.05.015

R. Grenningloh, T. Tai, N. Frahm, T. Hongo, A. Chicoine et al., Ets-1 Maintains IL-7 Receptor Expression in Peripheral T Cells, The Journal of Immunology, vol.186, issue.2, pp.969-976, 2011.
DOI : 10.4049/jimmunol.1002099

I. Cowell, A. Skinner, and H. Hurst, Transcriptional repression by a novel member of the bZIP family of transcription factors., Molecular and Cellular Biology, vol.12, issue.7, pp.3070-3077, 1992.
DOI : 10.1128/MCB.12.7.3070

V. Male, I. Nisoli, D. Gascoyne, and H. Brady, E4BP4: an unexpected player in the immune response, Trends in Immunology, vol.33, issue.2, pp.98-102, 2012.
DOI : 10.1016/j.it.2011.10.002

@. Gascoyne, D. Long, E. Veiga-fernandes, H. , D. Boer et al., The basic leucine zipper transcription factor E4BP4 is essential for natural killer cell development, Nature Immunology, vol.174, issue.10, pp.1118-1124, 2009.
DOI : 10.1073/pnas.0506306102

@. Kamizono, S. Duncan, G. Seidel, M. Morimoto, A. Hamada et al., Nfil3/E4bp4 is required for the development and maturation of NK cells in vivo, The Journal of Experimental Medicine, vol.15, issue.13, pp.2977-2986, 2009.
DOI : 10.1006/bbrc.1997.6206

M. Kashiwada, D. Levy, L. Mckeag, K. Murray, A. Schröder et al., IL-4-induced transcription factor NFIL3/E4BP4 controls IgE class switching, With ??32 identification of critical role for Nfil3, pp.821-826, 2010.
DOI : 10.1073/pnas.0909235107
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2818942

J. Santo, A defining factor for natural killer cell development, Nature Immunology, vol.33, issue.10, pp.1051-1052, 2009.
DOI : 10.1038/ni1009-1051

M. Townsend, A. Weinmann, J. Matsuda, R. Salomon, P. Farnham et al., T-bet Regulates the Terminal Maturation and Homeostasis of NK and V??14i NKT Cells, Immunity, vol.20, issue.4, pp.477-94, 2004.
DOI : 10.1016/S1074-7613(04)00076-7

C. Jenne, A. Enders, R. Rivera, S. Watson, A. Bankovich et al., expression in NK cells promotes egress from lymph nodes and bone marrow, The Journal of Experimental Medicine, vol.146, issue.11, pp.2469-2481, 2009.
DOI : 10.4049/jimmunol.175.11.7419
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768857

L. Naiche, Z. Harrelson, R. Kelly, and V. Papaioannou, T-Box Genes in Vertebrate Development, Annual Review of Genetics, vol.39, issue.1, pp.219-239, 2005.
DOI : 10.1146/annurev.genet.39.073003.105925
URL : https://hal.archives-ouvertes.fr/hal-00117154

A. Intlekofer, N. Takemoto, E. Wherry, S. Longworth, J. Northrup et al., Effector and memory CD8+ T cell fate coupled by T-bet and eomesodermin, Nature Immunology, vol.174, issue.12, pp.1236-1244, 2005.
DOI : 10.1038/ni1268

F. Cruz-guilloty, M. Pipkin, I. Djuretic, D. Levanon, J. Lotem et al., Runx3 and T-box proteins cooperate to establish the transcriptional program of effector CTLs, The Journal of Experimental Medicine, vol.206, issue.1, pp.51-59, 2009.
DOI : 10.1093/nar/gkl006

@. Gordon, S. Chaix, J. Rupp, L. Wu, J. Madera et al., The Transcription Factors T-bet and Eomes Control Key Checkpoints of Natural Killer Cell Maturation, Immunity, vol.36, issue.1, pp.55-67, 2012.
DOI : 10.1016/j.immuni.2011.11.016

K. Takeda, E. Cretney, Y. Hayakawa, T. Ota, H. Akiba et al., TRAIL identifies immature natural killer cells in newborn mice and adult mouse liver, Blood, vol.105, issue.5, pp.2082-2091, 2005.
DOI : 10.1182/blood-2004-08-3262

S. Samson, O. Richard, M. Tavian, T. Ranson, C. Vosshenrich et al., GATA-3 Promotes Maturation, IFN-?? Production, and Liver-Specific Homing of NK Cells, Immunity, vol.19, issue.5, pp.701-711, 2003.
DOI : 10.1016/S1074-7613(03)00294-2

C. Vosshenrich, M. García-ojeda, S. Samson-villéger, V. Pasqualetto, L. Enault et al., Erratum: A thymic pathway of mouse natural killer cell development characterized by expression of GATA-3 and CD127, Nature Immunology, vol.7, issue.12, pp.1217-1224, 2006.
DOI : 10.1038/ni1206-1343b

E. Rothenberg, Transcriptional drivers of the T-cell lineage program, Current Opinion in Immunology, vol.24, issue.2
DOI : 10.1016/j.coi.2011.12.012

@. Hoyler, T. Klose, C. Souabni, A. Turqueti-neves, A. Pfeifer et al., The Transcription Factor GATA-3 Controls Cell Fate and Maintenance of Type 2 Innate Lymphoid Cells, Immunity, vol.37, issue.4, pp.634-648, 2012.
DOI : 10.1016/j.immuni.2012.06.020

@. Mjösberg, J. Bernink, J. Golebski, K. Karrich, J. Peters et al., The Transcription Factor GATA3 Is Essential for the Function of Human Type 2 Innate Lymphoid Cells, Immunity, vol.37, issue.4, pp.649-659, 2012.
DOI : 10.1016/j.immuni.2012.08.015

@. Ribeiro, V. Hasan, M. Wilson, A. Boucontet, L. Pereira et al., Cutting Edge: Thymic NK Cells Develop Independently from T Cell Precursors, The Journal of Immunology, vol.185, issue.9, pp.4993-4997, 2010.
DOI : 10.4049/jimmunol.1002273
URL : https://hal.archives-ouvertes.fr/pasteur-00528741

K. Wolterink, R. García-ojeda, M. Vosshenrich, C. Hendriks, R. et al., The intrathymic crossroads of T and NK cell differentiation, Immunological Reviews, vol.277, issue.1, pp.126-137, 2010.
DOI : 10.1111/j.1600-065X.2010.00960.x
URL : https://hal.archives-ouvertes.fr/pasteur-01488625

E. Narni-mancinelli, B. Jaeger, C. Bernat, A. Fenis, S. Kung et al., Tuning of Natural Killer Cell Reactivity by NKp46 and Helios Calibrates T Cell Responses, Science, vol.335, issue.6066, pp.344-348, 2012.
DOI : 10.1126/science.1215621
URL : https://hal.archives-ouvertes.fr/hal-00685893

S. Ohno, T. Sato, K. Kohu, K. Takeda, K. Okumura et al., Runx proteins are involved in regulation of CD122, Ly49 family and IFN-?? expression during NK cell differentiation, International Immunology, vol.20, issue.1, pp.71-79, 2008.
DOI : 10.1093/intimm/dxm120

C. Lai and D. Mager, Role of Runt-related Transcription Factor 3 (RUNX3) in Transcription Regulation of Natural Cytotoxicity Receptor 1 (NCR1/NKp46), an Activating Natural Killer (NK) Cell Receptor, Journal of Biological Chemistry, vol.287, issue.10, pp.7324-7334, 2012.
DOI : 10.1074/jbc.M111.306936

S. Nutt, N. Taubenheim, J. Hasbold, L. Corcoran, and P. Hodgkin, The genetic network controlling plasma cell differentiation, Seminars in Immunology, vol.23, issue.5, pp.341-349, 2011.
DOI : 10.1016/j.smim.2011.08.010

A. Xin, S. Nutt, G. Belz, A. Kallies, M. Smith et al., Blimp1: Driving Terminal Differentiation to a T, SL: A role for Blimp1 in the transcriptional network controlling natural killer cell maturation, pp.85-100, 2010.
DOI : 10.1007/978-1-4419-5632-3_8

@. Van-gisbergen, K. Kragten, N. Hertoghs, K. Wensveen, F. Jonjic et al., Mouse Hobit is a homolog of the transcriptional repressor Blimp-1 that regulates NKT cell effector differentiation, Nature Immunology, vol.181, issue.9, pp.864-871, 2012.
DOI : 10.1016/j.micinf.2006.12.003

@. Lee, J. Cella, M. Mcdonald, K. Garlanda, C. Kennedy et al., AHR drives the development of gut ILC22 cells and postnatal lymphoid tissues via pathways dependent on and independent of Notch, Nature Immunology, vol.181, issue.2, pp.144-151, 2012.
DOI : 10.1007/s00281-009-0163-6

@. Possot, C. Schmutz, S. Chea, S. Boucontet, L. et al., Notch signaling is necessary for adult, but not fetal, development of ROR??t+ innate lymphoid cells, Nature Immunology, vol.11, issue.10, pp.949-958, 2011.
DOI : 10.1038/ni.2105

@. Cherrier, M. Sawa, S. Eberl, and G. , Notch, Id2, and ROR??t sequentially orchestrate the fetal development of lymphoid tissue inducer cells, The Journal of Experimental Medicine, vol.209, issue.4, pp.729-740, 2012.
DOI : 10.4049/jimmunol.170.12.5834

F. Radtke, A. Wilson, G. Stark, M. Bauer, J. Van-meerwijk et al., Deficient T Cell Fate Specification in Mice with an Induced Inactivation of Notch1, Immunity, vol.10, issue.5, pp.547-58, 1999.
DOI : 10.1016/S1074-7613(00)80054-0