M. M. Matzuk and D. J. Lamb, The biology of infertility: research advances and clinical challenges, Nature Medicine, vol.14, issue.11, pp.1197-1213, 2008.

M. Uhlen, L. Fagerberg, B. M. Hallstrom, C. Lindskog, P. Oksvold et al., Tissue-based map of the human proteome, Science, vol.347, issue.6220, pp.1260419-1260419, 2015.

H. J. Cooke and P. T. Saunders, Mouse models of male infertility, Nature Reviews Genetics, vol.3, issue.10, pp.790-801, 2002.

C. L. Borg, K. M. Wolski, G. M. Gibbs, and M. K. O'bryan, Phenotyping male infertility in the mouse: how to get the most out of a 'non-performer', Human Reproduction Update, vol.16, issue.2, pp.205-224, 2009.

G. Burgio, M. Szatanik, J. Guénet, M. R. Arnau, J. J. Panthier et al., Interspecific Recombinant Congenic Strains Between C57BL/6 and Mice of theMus spretusSpecies: A Powerful Tool to Dissect Genetic Control of Complex Traits, Genetics, vol.177, issue.4, pp.2321-2333, 2007.

D. L'hôte, P. Laissue, C. Serres, X. Montagutelli, R. A. Veitia et al., Interspecific resources: a major tool for quantitative trait locus cloning and speciation research, BioEssays, vol.32, issue.2, pp.132-142, 2010.

D. L'hôte, C. Serres, R. A. Veitia, X. Montagutelli, A. Oulmouden et al., Gene expression regulation in the context of mouse interspecific mosaic genomes, Genome Biology, vol.9, issue.8, p.R133, 2008.

D. L'hôte, M. Vatin, J. Auer, J. Castille, B. Passet et al., Fidgetin-Like1 Is a Strong Candidate for a Dynamic Impairment of Male Meiosis Leading to Reduced Testis Weight in Mice, PLoS ONE, vol.6, issue.11, p.e27582, 2011.

M. Vatin, G. Burgio, G. Renault, P. Laissue, V. Firlej et al., Refined Mapping of a Quantitative Trait Locus on Chromosome 1 Responsible for Mouse Embryonic Death, PLoS ONE, vol.7, issue.8, p.e43356, 2012.
URL : https://hal.archives-ouvertes.fr/pasteur-02552658

P. Laissue, B. Lakhal, M. Vatin, F. Batista, G. Burgio et al., Association of FOXD1 variants with adverse pregnancy outcomes in mice and humans, Open Biology, vol.6, issue.10, p.160109, 2016.
URL : https://hal.archives-ouvertes.fr/inserm-01399338

M. Vatin, S. Bouvier, L. Bellazi, X. Montagutelli, P. Laissue et al., Polymorphisms of Human Placental Alkaline Phosphatase Are Associated with in Vitro Fertilization Success and Recurrent Pregnancy Loss, The American Journal of Pathology, vol.184, issue.2, pp.362-368, 2014.
URL : https://hal.archives-ouvertes.fr/hal-01943648

M. Vatin, S. Bouvier, L. Bellazi, X. Montagutelli, P. Laissue et al., Polymorphisms of Human Placental Alkaline Phosphatase Are Associated with in Vitro Fertilization Success and Recurrent Pregnancy Loss, The American Journal of Pathology, vol.184, issue.2, pp.362-368, 2014.
URL : https://hal.archives-ouvertes.fr/hal-01943648

J. Yuan and J. Chen, FIGNL1-containing protein complex is required for efficient homologous recombination repair, Proceedings of the National Academy of Sciences, vol.110, issue.26, pp.10640-10645, 2013.

D. H. Kim, D. S. Ko, H. C. Lee, H. C. Lee, W. I. Park et al., Comparison of Maturation, Fertilization, Development, and Gene Expression of Mouse Oocytes Grown In Vitro and In Vivo, Journal of Assisted Reproduction and Genetics, vol.21, issue.7, pp.233-240, 2004.

S. Barbaux, C. Ialy-radio, M. Chalbi, E. Dybal, M. Homps-legrand et al., Sperm SPACA6 protein is required for mammalian Sperm-Egg Adhesion/Fusion, Scientific Reports, vol.10, issue.1, 2020.
URL : https://hal.archives-ouvertes.fr/inserm-02538018

M. Valdivia, T. Sillerico, A. D. Ioannes, and C. Barros, Proteolytic activity of rabbit perivitelline spermatozoa, Zygote, vol.7, issue.2, pp.143-149, 1999.

L. E. Clift, P. Andrlikova, M. Frolikova, P. Stopka, J. Bryja et al., Absence of spermatozoal CD46 protein expression and associated rapid acrosome reaction rate in striped field mice (Apodemus agrarius), Reproductive Biology and Endocrinology, vol.7, issue.1, p.29, 2009.

N. Sebkova, L. Ded, K. Vesela, and K. Dvorakova-hortova, Progress of sperm IZUMO1 relocation during spontaneous acrosome reaction, REPRODUCTION, vol.147, issue.2, pp.231-240, 2014.

A. Wiser, S. Sachar, Y. Ghetler, A. Shulman, and H. Breitbart, Assessment of sperm hyperactivated motility and acrosome reaction can discriminate the use of spermatozoa for conventionalin vitrofertilisation or intracytoplasmic sperm injection: Preliminary results, Andrologia, vol.46, issue.3, pp.313-315, 2013.

M. Efrat, A. Stein, H. Pinkas, H. Breitbart, R. Unger et al., Paraoxonase 1 (PON1) attenuates sperm hyperactivity and spontaneous acrosome reaction, Andrology, vol.7, issue.1, pp.24-30, 2018.

N. Inoue, M. Ikawa, T. Nakanishi, M. Matsumoto, M. Nomura et al., Disruption of Mouse CD46 Causes an Accelerated Spontaneous Acrosome Reaction in Sperm, Molecular and Cellular Biology, vol.23, issue.7, pp.2614-2622, 2003.

J. A. Crapster, P. G. Rack, Z. J. Hellmann, A. D. Le, C. M. Adams et al., HIPK4 is essential for murine spermiogenesis, eLife, vol.9, 2020.

C. Liu, Z. Song, L. Wang, H. Yu, W. Liu et al., Sirt1 regulates acrosome biogenesis by modulating autophagic flux during spermiogenesis in mice, Development, vol.144, issue.3, pp.441-451, 2016.

R. Harbuz, R. Zouari, V. Pierre, M. Ben khelifa, M. Kharouf et al., A Recurrent Deletion of DPY19L2 Causes Infertility in Man by Blocking Sperm Head Elongation and Acrosome Formation, The American Journal of Human Genetics, vol.88, issue.3, pp.351-361, 2011.
URL : https://hal.archives-ouvertes.fr/inserm-00588067

V. Pierre, G. Martinez, C. Coutton, J. Delaroche, S. Yassine et al., Absence of Dpy19l2, a new inner nuclear membrane protein, causes globozoospermia in mice by preventing the anchoring of the acrosome to the nucleus, Development, vol.139, issue.16, pp.2955-2965, 2012.

S. J. Ye, L. Ying, S. Ghosh, L. R. De-frança, and L. D. Russell, Sertoli cell cycle: A re-examination of the structural changes during the cycle of the seminiferous epithelium of the rat, The Anatomical Record, vol.237, issue.2, pp.187-198, 1993.

G. Berruti, L. Perego, and E. Martegani, Molecular Cloning and Developmental Pattern of Expression of MSJ-1, a New Male Germ Cell-Specific DnaJ Homologue, Advances in Experimental Medicine and Biology, vol.444, pp.145-151, 1998.

R. Meccariello, G. Cobellis, G. Berruti, M. P. Junier, M. Ceriani et al., Mouse Sperm Cell-Specific DnaJ First Homologue: An Evolutionarily Conserved Protein for Spermiogenesis1, Biology of Reproduction, vol.66, issue.5, pp.1328-1335, 2002.

R. Meccariello, G. Berruti, R. Chianese, R. De-santis, F. Di-cunto et al., Structure of msj-1 gene in mice and humans: A possible role in the regulation of male reproduction, General and Comparative Endocrinology, vol.156, issue.1, pp.91-103, 2008.

M. Abu-farha, P. Cherian, I. Al-khairi, A. Tiss, A. Khadir et al., DNAJB3/HSP-40 cochaperone improves insulin signaling and enhances glucose uptake in vitro through JNK repression, Scientific Reports, vol.5, issue.1, 2015.

S. Boillée, G. Berruti, R. Meccariello, G. Grannec, F. Razan et al., Early defect in the expression of mouse sperm DnaJ 1, a member of the DNAJ/heat shock protein 40 chaperone protein family, in the spinal cord of the wobbler mouse, a murine model of motoneuronal degeneration, Neuroscience, vol.113, issue.4, pp.825-835, 2002.

J. A. Gaasch, A. B. Bolwahnn, and J. Suzanne-lindsey, Hepatocyte growth factor-regulated genes in differentiated RAW 264.7 osteoclast and undifferentiated cells, Gene, vol.369, pp.142-152, 2006.

R. Mitsugi, T. Itoh, and R. Fujiwara, Expression of Human DNAJ (Heat Shock Protein-40) B3 in Humanized UDP-glucuronosyltransferase 1 Mice, International Journal of Molecular Sciences, vol.16, issue.12, pp.14997-15008, 2015.

G. Berruti and E. Martegani, The Deubiquitinating Enzyme mUBPy Interacts with the Sperm-Specific Molecular Chaperone MSJ-1: The Relation with the Proteasome, Acrosome, and Centrosome in Mouse Male Germ Cells1, Biology of Reproduction, vol.72, issue.1, pp.14-21, 2005.

A. Arredouani, A. Diane, N. Khattab, I. Bensmail, I. Aoude et al., DNAJB3 attenuates metabolic stress and promotes glucose uptake by eliciting Glut4 translocation, Scientific Reports, vol.9, issue.1, p.4772, 2019.

J. C. Van-de-weghe, T. D. Rusterholz, B. Latour, M. E. Grout, K. A. Aldinger et al., Mutations in ARMC9 , which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish, The American Journal of Human Genetics, vol.101, issue.1, pp.23-36, 2017.

S. Brownlow, R. Webster, R. Croxen, M. Brydson, B. Neville et al., Acetylcholine receptor ? subunit mutations underlie a fast-channel myasthenic syndrome and arthrogryposis multiplex congenita, Journal of Clinical Investigation, vol.108, issue.1, pp.125-130, 2001.

X. M. Shen, T. Fukuda, K. Ohno, S. M. Sine, and A. G. Engel, Congenital myasthenia?related AChR ? subunit mutation interferes with intersubunit communication essential for channel gating, Journal of Clinical Investigation, vol.118, issue.5, pp.1867-1876, 2008.

X. M. Shen, K. Ohno, T. Fukudome, A. Tsujino, J. M. Brengman et al., Congenital myasthenic syndrome caused by low-expressor fast-channel AChR subunit mutation, Neurology, vol.59, issue.12, pp.1881-1888, 2002.

B. Lassalle, H. Bastos, J. P. Louis, L. Riou, J. Testart et al., `Side Population' cells in adult mouse testis express Bcrp1 gene and are enriched in spermatogonia and germinal stem cells, Development, vol.131, issue.2, pp.479-487, 2003.
URL : https://hal.archives-ouvertes.fr/hal-00095056