H. White-cooper and N. Bausek, Evolution and spermatogenesis, Philos Trans R Soc Lond Ser B Biol Sci, vol.365, pp.1465-80, 1546.

S. Bhasin, C. Mallidis, and K. Ma, The genetic basis of infertility in men, Baillieres Best Pract Res Clin Endocrinol Metab, vol.14, issue.3, pp.363-88, 2000.

A. Rosenstrauch, S. Weil, A. A. Degen, and M. Friedlander, Leydig cell functional structure and plasma androgen level during the decline in fertility in aging roosters, Gen Comp Endocrinol, vol.109, issue.2, pp.251-259, 1998.

C. E. Beaupre, C. J. Tressler, S. J. Beaupre, J. L. Morgan, W. G. Bottje et al., Determination of testis temperature rhythms and effects of constant light on testicular function in the domestic fowl (Gallus domesticus), Biol Reprod, vol.56, issue.6, pp.1570-1575, 1997.

M. R. Bakst, V. Akuffo, P. Trefil, and J. P. Brillard, Morphological and histochemical characterization of the seminiferous epithelial and Leydig cells of the Turkey, Anim Reprod Sci, vol.97, issue.3-4, pp.303-316, 2007.

M. De-reviers, M. T. Hochereau-de-reviers, M. R. Blanc, J. P. Brillard, M. Courot et al., Control of Sertoli and germ cell populations in the cock and sheep testes, Reprod Nutr Dev, vol.20, issue.1b, pp.241-250, 1980.
URL : https://hal.archives-ouvertes.fr/hal-00897635

H. Wilson, N. Piesco, E. Miller, and W. Nesbeth, Prediction of the fertility potential of broiler breeder males, Worlds Poult Sci J, vol.35, issue.2, pp.95-118, 1979.

A. Rosenstrauch, A. A. Degen, and M. Friedlander, Spermatozoa retention by Sertoli cells during the decline in fertility in aging roosters, Biol Reprod, vol.50, issue.1, pp.129-165, 1994.

E. Bonilla and E. Y. Xu, Identification and characterization of novel mammalian spermatogenic genes conserved from fly to human, Mol Hum Reprod, vol.14, issue.3, pp.137-179, 2008.

E. B. Rodgers-melnick and R. K. Naz, Male-biased genes of Drosophila melanogaster that are conserved in mammalian testis, Front Biosci (Elite Ed, vol.2, pp.841-849, 2010.

E. Y. Xu, D. F. Lee, A. Klebes, P. J. Turek, T. B. Kornberg et al., Human BOULE gene rescues meiotic defects in infertile flies, Hum Mol Genet, vol.12, issue.2, pp.169-75, 2003.

S. Bonaccorsi, M. G. Giansanti, and M. Gatti, Spindle self-organization and cytokinesis during male meiosis in asterless mutants of Drosophila melanogaster, J Cell Biol, vol.142, issue.3, pp.751-61, 1998.

G. F. Barbato, Genetic relationships between selection for growth and reproductive effectiveness, Poult Sci, vol.78, issue.3, pp.444-52, 1999.

X. Y. Zhang, M. Q. Wu, S. Z. Wang, H. Zhang, Z. Q. Du et al., Genetic selection on abdominal fat content alters the reproductive performance of broilers, Animal, vol.12, issue.6, pp.1232-1273, 2018.

S. Elis, A. Desmarchais, E. Cardona, S. Fouchecourt, R. Dalbies-tran et al., Genes involved in Drosophila melanogaster ovarian function are highly conserved throughout evolution, Genome Biol Evol, vol.10, issue.10, pp.2629-2671, 2018.
URL : https://hal.archives-ouvertes.fr/hal-01991460

S. Dade, I. Callebaut, P. Mermillod, and P. Monget, Identification of a new expanding family of genes characterized by atypical LRR domains. Localization of a cluster preferentially expressed in oocyte, FEBS Lett, vol.555, issue.3, pp.533-541, 2003.

S. Dade, I. Callebaut, A. Paillisson, M. Bontoux, R. Dalbies-tran et al., In silico identification and structural features of six new genes similar to MATER specifically expressed in the oocyte, Biochem Biophys Res Commun, vol.324, issue.2, pp.547-53, 2004.
URL : https://hal.archives-ouvertes.fr/hal-00086729

A. Paillisson, S. Dade, I. Callebaut, M. Bontoux, R. Dalbies-tran et al., Identification, characterization and metagenome analysis of oocyte-specific genes organized in clusters in the mouse genome, BMC Genomics, vol.6, p.76, 2005.
URL : https://hal.archives-ouvertes.fr/inserm-00090516

A. Paillisson, A. Levasseur, P. Gouret, I. Callebaut, M. Bontoux et al., Bromodomain testis-specific protein is expressed in mouse oocyte and evolves faster than its ubiquitously expressed paralogs BRD2, ?3, and ?4, Genomics, vol.89, issue.2, pp.215-238, 2007.
URL : https://hal.archives-ouvertes.fr/hal-00131215

C. I. Castillo-davis and D. L. Hartl, Conservation, relocation and duplication in genome evolution, Trends Genet, vol.19, issue.11, pp.593-600, 2003.

E. K. Maxwell, C. E. Schnitzler, P. Havlak, N. H. Putnam, A. D. Nguyen et al., Evolutionary profiling reveals the heterogeneous origins of classes of human disease genes: implications for modeling disease genetics in animals, BMC Evol Biol, vol.14, p.212, 2014.

C. Lethimonier, T. Madigou, J. A. Munoz-cueto, J. J. Lareyre, and O. Kah, Evolutionary aspects of GnRHs, GnRH neuronal systems and GnRH receptors in teleost fish, Gen Comp Endocrinol, vol.135, issue.1, pp.1-16, 2004.
URL : https://hal.archives-ouvertes.fr/hal-00295299

M. Marvel, O. S. Spicer, T. T. Wong, N. Zmora, and Y. Zohar, Knockout of the Gnrh genes in zebrafish: effects on reproduction and potential compensation by reproductive and feeding-related neuropeptides, Biol Reprod, vol.99, issue.3, pp.565-77, 2018.

A. Rodriguez-mari, C. Canestro, R. A. Bremiller, J. M. Catchen, Y. L. Yan et al., Retinoic acid metabolic genes, meiosis, and gonadal sex differentiation in zebrafish, PLoS One, vol.8, issue.9, p.73951, 2013.

C. A. Wilson, S. K. High, B. M. Mccluskey, A. Amores, Y. L. Yan et al., Wild sex in zebrafish: loss of the natural sex determinant in domesticated strains, Genetics, vol.198, issue.3, pp.1291-308, 2014.
URL : https://hal.archives-ouvertes.fr/hal-01205119

A. Force, M. Lynch, F. B. Pickett, A. Amores, Y. L. Yan et al., Preservation of duplicate genes by complementary, degenerative mutations, Genetics, vol.151, issue.4, pp.1531-1576, 1999.

C. Meslin, C. Desert, I. Callebaut, A. Djari, C. Klopp et al., Expanding duplication of free fatty acid receptor-2 (GPR43) genes in the chicken genome, Genome Biol Evol, vol.7, issue.5, pp.1332-1380, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01157691

C. Olesen, M. Moller, and A. G. Byskov, Tesmin transcription is regulated differently during male and female meiosis, Mol Reprod Dev, vol.67, issue.1, pp.116-142, 2004.

H. Inoue, N. Ogonuki, M. Hirose, Y. Hatanaka, S. Matoba et al., Mouse D1Pas1, a DEAD-box RNA helicase, is required for the completion of first meiotic prophase in male germ cells, Biochem Biophys Res Commun, vol.478, issue.2, pp.592-600, 2016.

D. Liu, M. M. Matzuk, W. K. Sung, Q. Guo, P. Wang et al., Cyclin A1 is required for meiosis in the male mouse, Nat Genet, vol.20, issue.4, pp.377-80, 1998.

F. Baudat, Y. Imai, and B. De-massy, Meiotic recombination in mammals: localization and regulation, Nat Rev Genet, vol.14, issue.11, pp.794-806, 2013.
URL : https://hal.archives-ouvertes.fr/hal-00875210

U. Schlecht, P. Demougin, R. Koch, L. Hermida, C. Wiederkehr et al., Expression profiling of mammalian male meiosis and gametogenesis identifies novel candidate genes for roles in the regulation of fertility, Mol Biol Cell, vol.15, issue.3, pp.1031-1074, 2004.

W. Yan, L. Ma, K. H. Burns, and M. M. Matzuk, Haploinsufficiency of kelch-like protein homolog 10 causes infertility in male mice, Proc Natl Acad Sci U S A, vol.101, issue.20, pp.7793-7801, 2004.

E. Gob, J. Schmitt, R. Benavente, and M. Alsheimer, Mammalian sperm head formation involves different polarization of two novel LINC complexes, PLoS One, vol.5, issue.8, p.12072, 2010.

M. P. Kracklauer, H. M. Wiora, W. J. Deery, X. Chen, B. Bolival et al., The Drosophila SUN protein Spag4 cooperates with the coiled-coil protein Yuri Gagarin to maintain association of the basal body and spermatid nucleus, J Cell Sci, vol.123, pp.2763-72, 2010.

Y. Shang, F. Zhu, L. Wang, Y. C. Ouyang, M. Z. Dong et al., Essential role for SUN5 in anchoring sperm head to the tail, Elife, vol.6, p.28199, 2017.

Y. Inaba, K. Shinohara, Y. Botilde, R. Nabeshima, K. Takaoka et al., Transport of the outer dynein arm complex to cilia requires a cytoplasmic protein Lrrc6, Genes Cells, vol.21, issue.7, pp.728-767, 2016.

E. Kott, P. Duquesnoy, B. Copin, M. Legendre, D. Moal et al., Loss-of-function mutations in LRRC6, a gene essential for proper axonemal assembly of inner and outer dynein arms, cause primary ciliary dyskinesia, Am J Hum Genet, vol.91, issue.5, pp.958-64, 2012.

D. J. Moore, A. Onoufriadis, A. Shoemark, M. A. Simpson, P. I. Zur-lage et al., Mutations in ZMYND10, a gene essential for proper axonemal assembly of inner and outer dynein arms in humans and flies, cause primary ciliary dyskinesia, Am J Hum Genet, vol.93, issue.2, pp.346-56, 2013.

M. A. Zariwala, H. Y. Gee, M. Kurkowiak, A. Da, M. W. Leigh et al., ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6, Am J Hum Genet, vol.93, issue.2, pp.336-381, 2013.

K. Ikegami and M. Setou, TTLL10 can perform tubulin glycylation when coexpressed with TTLL8, FEBS Lett, vol.583, issue.12, pp.1957-63, 2009.

J. Van-dijk, K. Rogowski, J. Miro, B. Lacroix, B. Edde et al., A targeted multienzyme mechanism for selective microtubule polyglutamylation, Mol Cell, vol.26, issue.3, pp.437-485, 2007.
URL : https://hal.archives-ouvertes.fr/hal-00217041

I. S. Gul, P. Hulpiau, Y. Saeys, and F. Van-roy, Metazoan evolution of the armadillo repeat superfamily, Cell Mol Life Sci, vol.74, issue.3, pp.525-566, 2017.

W. Cheng, Y. T. Ip, and Z. Xu, Gudu, an Armadillo repeat-containing protein, is required for spermatogenesis in Drosophila, Gene, vol.531, issue.2, pp.294-300, 2013.

H. Pausch, H. Venhoranta, C. Wurmser, K. Hakala, T. Iso-touru et al., A frameshift mutation in ARMC3 is associated with a tail stump sperm defect in Swedish Red (Bos taurus) cattle, BMC Genet, vol.17, p.49, 2016.

A. K. Lim and T. Kai, Unique germ-line organelle, nuage, functions to repress selfish genetic elements in Drosophila melanogaster, Proc Natl Acad Sci, vol.104, issue.16, pp.6714-6723, 2007.

J. Pan, M. Goodheart, S. Chuma, N. Nakatsuji, D. C. Page et al., RNF17, a component of the mammalian germ cell nuage, is essential for spermiogenesis, Development, vol.132, issue.18, pp.4029-4068, 2005.

D. W. Houston and M. L. King, Germ plasm and molecular determinants of germ cell fate, Curr Top Dev Biol, vol.50, pp.155-81, 2000.

E. Voronina, G. Seydoux, P. Sassone-corsi, and I. Nagamori, RNA granules in germ cells, Cold Spring Harb Perspect Biol, vol.3, issue.12, p.2774, 2011.

X. F. Fu, S. F. Cheng, L. Q. Wang, S. Yin, D. Felici et al., DAZ family proteins, key players for germ cell development, Int J Biol Sci, vol.11, issue.10, pp.1226-1261, 2015.

C. Krausz and E. Casamonti, Spermatogenic failure and the Y chromosome, Hum Genet, vol.136, issue.5, pp.637-55, 2017.

J. Legrand and R. M. Hobbs, RNA processing in the male germline: mechanisms and implications for fertility, Semin Cell Dev Biol, vol.79, pp.80-91, 2018.

Y. Yabuta, H. Ohta, T. Abe, K. Kurimoto, S. Chuma et al., TDRD5 is required for retrotransposon silencing, chromatoid body assembly, and spermiogenesis in mice, J Cell Biol, vol.192, issue.5, pp.781-95, 2011.

S. Kashiwabara, S. Tsuruta, K. Okada, A. Saegusa, Y. Miyagaki et al., Functional compensation for the loss of testis-specific poly(A)-binding protein, PABPC2, during mouse spermatogenesis, J Reprod Dev, vol.62, issue.3, pp.305-315, 2016.

C. Lim, L. Tarayrah, and X. Chen, Transcriptional regulation during Drosophila spermatogenesis, Spermatogenesis, vol.2, issue.3, pp.158-66, 2012.

S. Y. Yang, E. M. Baxter, and M. Van-doren, Phf7 controls male sex determination in the Drosophila germline, Dev Cell, vol.22, issue.5, pp.1041-51, 2012.

T. Zhang, M. W. Murphy, M. D. Gearhart, V. J. Bardwell, and D. Zarkower, The mammalian Doublesex homolog DMRT6 coordinates the transition between mitotic and meiotic developmental programs during spermatogenesis, Development, vol.141, pp.3662-71, 2014.

J. Merkin, C. Russell, P. Chen, and C. B. Burge, Evolutionary dynamics of gene and isoform regulation in mammalian tissues, Science, vol.338, issue.6114, pp.1593-1602, 2012.

J. Pasquier, C. Cabau, T. Nguyen, E. Jouanno, D. Severac et al., Gene evolution and gene expression after whole genome duplication in fish: the PhyloFish database, BMC Genomics, vol.17, p.368, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01487023

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