N. Hunter, Meiotic Recombination, Molecular Genetics of Recombination, pp.381-442, 2007.

N. H. Barton and B. Charlesworth, Why sex and recombination? Science, vol.281, p.9748151, 1998.

M. S. Brown and D. K. Bishop, DNA strand exchange and RecA homologs in meiosis. Cold Spring Harb Perspect Biol, vol.7, p.25475089, 2014.

N. Hunter, Meiotic Recombination: The Essence of Heredity, Cold Spring Harb Perspect Biol, vol.7, p.26511629, 2015.

D. Zickler and N. Kleckner, Recombination, Pairing, and Synapsis of Homologs during Meiosis, Cold Spring Harb Perspect Biol, vol.7, p.25986558, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01199651

M. Serrentino and V. Borde, The spatial regulation of meiotic recombination hotspots: are all DSB hotspots crossover hotspots? Exp Cell Res, vol.318, p.22487095, 2012.

S. K. Godin, M. R. Sullivan, and K. A. Bernstein, Novel insights into RAD51 activity and regulation during homologous recombination and DNA replication, Biochem Cell Biol, vol.94, p.27224545, 2016.

M. R. Taylor, M. Spirek, J. Ma, C. Carzaniga, R. Takaki et al., A Polar and NucleotideDependent Mechanism of Action for RAD51 Paralogs in RAD51 Filament Remodeling, Mol Cell, vol.64, p.27867009, 2016.

H. Su, Z. Cheng, J. Huang, J. Lin, G. P. Copenhaver et al., Arabidopsis RAD51, RAD51C and XRCC3 proteins form a complex and facilitate RAD51 localization on chromosomes for meiotic recombination, PLoS Genet, vol.13, p.28562599, 2017.

N. Suwaki, K. Klare, and M. Tarsounas, RAD51 paralogs: roles in DNA damage signalling, recombinational repair and tumorigenesis, Semin Cell Dev Biol, vol.22, p.21821141, 2011.

A. Zelensky, R. Kanaar, and C. Wyman, Mediators of homologous DNA pairing, Cold Spring Harb Perspect Biol, vol.6, p.25301930, 2014.

D. K. Bishop, D. Park, L. Xu, and N. Kleckner, DMC1: a meiosis-specific yeast homolog of E. coli recA required for recombination, synaptonemal complex formation, and cell cycle progression, Cell, vol.69, p.1581960, 1992.

J. C. Game and R. K. Mortimer, A genetic study of x-ray sensitive mutants in yeast, Mutat Res, vol.24, p.4606119, 1974.

J. C. Game, T. J. Zamb, R. J. Braun, M. Resnick, and R. M. Roth, The Role of Radiation (rad) Genes in Meiotic Recombination in Yeast, Genetics, vol.94, p.17248996, 1980.

A. Aboussekhra, R. Chanet, A. Adjiri, and F. Fabre, Semidominant suppressors of Srs2 helicase mutations of Saccharomyces cerevisiae map in the RAD51 gene, whose sequence predicts a protein with similarities to procaryotic RecA proteins, Mol Cell Biol. 1992, vol.12, p.1620127

A. Shinohara, H. Ogawa, and T. Ogawa, Rad51 protein involved in repair and recombination in S. cerevisiae is a RecA-like protein, Cell, vol.69, p.1581961, 1992.

Z. Lin, H. Kong, M. Nei, and H. Ma, Origins and evolution of the recA/RAD51 gene family: evidence for ancient gene duplication and endosymbiotic gene transfer, Proc Natl Acad Sci, vol.103, p.16798872, 2006.

M. A. Ramesh, S. Malik, and J. M. Logsdon, A phylogenomic inventory of meiotic genes; evidence for sex in Giardia and an early eukaryotic origin of meiosis, Curr Biol, vol.15, p.15668177, 2005.

N. Y. Stassen, J. M. Logsdon, G. J. Vora, H. H. Offenberg, J. D. Palmer et al., Isolation and characterization of rad51 orthologs from Coprinus cinereus and Lycopersicon esculentum, and phylogenetic analysis of eukaryotic recA homologs, Curr Genet, vol.31, p.9021132, 1997.

P. Baumann, F. E. Benson, and S. C. West, Human Rad51 protein promotes ATP-dependent homologous pairing and strand transfer reactions in vitro, Cell, vol.87, p.8929543, 1996.

E. L. Hong, A. Shinohara, and D. K. Bishop, Saccharomyces cerevisiae Dmc1 protein promotes renaturation of single-strand DNA (ssDNA) and assimilation of ssDNA into homologous super-coiled duplex DNA, J Biol Chem, vol.276, p.11551925, 2001.

Z. Li, E. I. Golub, R. Gupta, and C. M. Radding, Recombination activities of HsDmc1 protein, the meiotic human homolog of RecA protein, Proc Natl Acad Sci U S A, vol.94, p.9326590, 1997.

J. Y. Masson and S. C. West, The Rad51 and Dmc1 recombinases: a non-identical twin relationship, Trends Biochem Sci, vol.26, p.11166572, 2001.

S. D. Sheridan, X. Yu, R. Roth, J. E. Heuser, M. G. Sehorn et al., A comparative analysis of Dmc1 and Rad51 nucleoprotein filaments, Nucleic Acids Res, vol.36, p.18535008, 2008.

P. Sung, Catalysis of ATP-dependent homologous DNA pairing and strand exchange by yeast RAD51 protein. Science, vol.265, p.8066464, 1994.

W. Kagawa and H. Kurumizaka, From meiosis to postmeiotic events: uncovering the molecular roles of the meiosis-specific recombinase Dmc1, FEBS J, vol.277, pp.590-598, 2010.

D. V. Bugreev, R. J. Pezza, O. M. Mazina, O. N. Voloshin, R. D. Camerini-otero et al., The resistance of DMC1 D-loops to dissociation may account for the DMC1 requirement in meiosis, Nat Struct Mol Biol, vol.18, p.21151113, 2011.

A. Schwacha and N. Kleckner, Interhomolog bias during meiotic recombination: meiotic functions promote a highly differentiated interhomolog-only pathway, Cell, vol.90, p.9323140, 1997.

S. Hong, Y. Sung, M. Yu, M. Lee, N. Kleckner et al., The logic and mechanism of homologous recombination partner choice, Mol Cell, vol.51, p.23973374, 2013.

V. Cloud, Y. L. Chan, J. Grubb, B. Budke, and D. K. Bishop, Rad51 Is an Accessory Factor for Dmc1-Mediated Joint Molecule Formation During Meiosis, Science, vol.337, p.22955832, 2012.

O. Da-ines, F. Degroote, C. Goubely, S. Amiard, M. E. Gallego et al., Meiotic recombination in Arabidopsis is catalysed by DMC1, with RAD51 playing a supporting role, PLoS Genet, vol.9, p.24086145, 2013.
URL : https://hal.archives-ouvertes.fr/inserm-01907382

N. Hunter and N. Kleckner, The single-end invasion: an asymmetric intermediate at the double-strand break to double-holliday junction transition of meiotic recombination, Cell, vol.106, p.11461702, 2001.

B. Rockmill and G. S. Roeder, The yeast med1 mutant undergoes both meiotic homolog nondisjunction and precocious separation of sister chromatids, Genetics, vol.136, p.8138177, 1994.

B. Rockmill, M. Sym, H. Scherthan, and G. S. Roeder, Roles for two RecA homologs in promoting meiotic chromosome synapsis, Genes Dev, vol.9, p.7590245, 1995.

H. Tsubouchi and G. S. Roeder, The importance of genetic recombination for fidelity of chromosome pairing in meiosis, Dev Cell, vol.5, p.14667413, 2003.

D. L. Pittman, J. Cobb, K. J. Schimenti, L. A. Wilson, D. M. Cooper et al., Meiotic prophase arrest with failure of chromosome synapsis in mice deficient for Dmc1, a germline-specific RecA homolog, Mol Cell, vol.1, p.9660953, 1998.

K. Yoshida, G. Kondoh, Y. Matsuda, T. Habu, Y. Nishimune et al., The mouse RecA-like gene Dmc1 is required for homologous chromosome synapsis during meiosis, Mol Cell, vol.1, p.9660954, 1998.

D. S. Lim and P. Hasty, A mutation in mouse rad51 results in an early embryonic lethal that is suppressed by a mutation in p53, Mol Cell Biol, vol.16, p.8943369, 1996.

T. Tsuzuki, Y. Fujii, K. Sakumi, Y. Tominaga, K. Nakao et al., Targeted disruption of the Rad51 gene leads to lethality in embryonic mice, Proc Natl Acad Sci, vol.93, p.8692798, 1996.

J. Dai, O. Voloshin, S. Potapova, and R. D. Camerini-otero, Meiotic Knockdown and Complementation Reveals Essential Role of RAD51 in Mouse Spermatogenesis, Cell Rep, vol.18, p.28178517, 2017.

A. E. Franklin, J. Mcelver, I. Sunjevaric, R. Rothstein, B. Bowen et al., Three-dimensional microscopy of the Rad51 recombination protein during meiotic prophase, Plant Cell, vol.11, p.10330467, 1999.

J. Li, L. C. Harper, I. Golubovskaya, C. R. Wang, D. Weber et al., Functional analysis of maize RAD51 in meiosis and double-strand break repair, Genetics, vol.176, p.17507687, 2007.

C. Rajanikant, M. Melzer, B. J. Rao, and J. K. Sainis, Homologous recombination properties of OsRad51, a recombinase from rice, Plant Mol Biol, vol.68, p.18695945, 2008.

Y. Morozumi, R. Ino, S. Ikawa, N. Mimida, T. Shimizu et al., Homologous pairing activities of two rice RAD51 proteins, RAD51A1 and RAD51A2. PLoS One, vol.8, p.24124491, 2013.

Z. Y. Deng and T. Wang, OsDMC1 is required for homologous pairing in Oryza sativa, Plant Mol Biol, vol.65, p.17562186, 2007.

H. Wang, Q. Hu, D. Tang, X. Liu, G. Du et al., OsDMC1 Is Not Required for Homologous Pairing in Rice Meiosis, Plant Physiol, vol.171, p.26960731, 2016.

A. Kathiresan, G. S. Khush, and J. Bennet, Two rice DMC1 genes are differentially expressed during meiosis and during haploid and diploid mitosis, J Sex Plant Reprod, vol.14, pp.257-267, 2002.

Z. Ding, T. Wang, K. Chong, and S. Bai, Isolation and characterization of OsDMC1, the rice homologue of the yeast DMC1 gene essential for meiosis, J Sex Plant Reprod, vol.13, pp.285-288, 2001.

J. Shimazu, C. Matsukura, M. Senda, R. Ishikawa, S. Akada et al., Characterization of a DMC1 homologue, RiLIM15, in meiotic panicles, mitotic cultured cells and mature leaves of rice, Oryza sativa L.). Theor Appl Genet, vol.102, pp.1159-1163, 2001.

F. Couteau, F. Belzile, C. Horlow, O. Grandjean, D. Vezon et al., Random chromosome segregation without meiotic arrest in both male and female meiocytes of a dmc1 mutant of Arabidopsis, Plant Cell, vol.11, p.10488231, 1999.

W. Li, C. Chen, U. Markmann-mulisch, L. Timofejeva, E. Schmelzer et al., The Arabidopsis AtRAD51 gene is dispensable for vegetative development but required for meiosis, Proc Natl Acad Sci U S A, vol.101, p.15249667, 2004.

W. Kobayashi, S. Sekine, S. Machida, and H. Kurumizaka, Green fluorescent protein fused to the C terminus of RAD51 specifically interferes with secondary DNA binding by the RAD51-ssDNA complex, Genes Genet Syst, vol.89, p.25747041, 2014.

L. E. Berchowitz and G. P. Copenhaver, Fluorescent Arabidopsis tetrads: a visual assay for quickly developing large crossover and crossover interference data sets, Nat Protoc, vol.3, p.18193020, 2008.

N. E. Yelina, P. A. Ziolkowski, N. Miller, X. Zhao, K. A. Kelly et al., High-throughput analysis of meiotic crossover frequency and interference via flow cytometry of fluorescent pollen in Arabidopsis thaliana, Nat Protoc, vol.8, p.24113785, 2013.

E. Sanchez-moran, S. J. Armstrong, J. L. Santos, F. C. Franklin, and G. H. Jones, Chiasma formation in Arabidopsis thaliana accession Wassileskija and in two meiotic mutants, Chromosome Res, vol.9, p.11321367, 2001.

L. Chelysheva, D. Vezon, A. Chambon, G. Gendrot, L. Pereira et al., The Arabidopsis HEI10 Is a New ZMM Protein Related to Zip3, PLoS Genet, vol.8, p.22844245, 2012.
URL : https://hal.archives-ouvertes.fr/hal-01190765

J. D. Higgins, E. Sanchez-moran, S. J. Armstrong, G. H. Jones, and F. C. Franklin, The Arabidopsis synaptonemal complex protein ZYP1 is required for chromosome synapsis and normal fidelity of crossing over, Genes Dev, vol.19, p.16230536, 2005.

S. Armstrong, A time course for the analysis of meiotic progression in Arabidopsis thaliana, Plant Meiosis Methods in Molecular Biology (Methods and Protocols), pp.119-123, 2013.

D. Lydall, Y. Nikolsky, D. K. Bishop, and T. Weinert, A meiotic recombination checkpoint controlled by mitotic checkpoint genes, Nature, vol.383, p.8893012, 1996.

T. L. Callender, R. Laureau, L. Wan, X. Chen, R. Sandhu et al., Mek1 Down Regulates Rad51 Activity during Yeast Meiosis by Phosphorylation of Hed1, PLoS Genet. 2016, vol.12, p.27483004
URL : https://hal.archives-ouvertes.fr/hal-01375668

M. Kurzbauer, C. Uanschou, D. Chen, and P. Schlögelhofer, The recombinases DMC1 and RAD51 are functionally and spatially separated during meiosis in Arabidopsis, Plant Cell. 2012, vol.24, p.22589466

C. Uanschou, A. Ronceret, V. Harder, M. , D. Muyt et al., Sufficient amounts of functional HOP2/MND1 complex promote interhomolog DNA repair but are dispensable for intersister DNA repair during meiosis in Arabidopsis, Plant Cell, vol.25, p.24363313, 2013.
URL : https://hal.archives-ouvertes.fr/hal-01204161

M. Pradillo, E. López, R. Linacero, C. Romero, N. Cuñado et al., Together yes, but not coupled: new insights into the roles of RAD51 and DMC1 in plant meiotic recombination, Plant J, vol.69, p.22066484, 2012.

N. E. Yelina, K. Choi, L. Chelysheva, M. Macaulay, B. De-snoo et al., Epigenetic remodeling of meiotic crossover frequency in Arabidopsis thaliana DNA methyltransferase mutants, PLoS Genet, vol.8, p.22876192, 2012.
URL : https://hal.archives-ouvertes.fr/hal-01190760

S. Armstrong, A. Caryl, G. Jones, and F. Franklin, Asy1, a protein required for meiotic chromosome synapsis, localizes to axis-associated chromatin in Arabidopsis and Brassica, J Cell Sci, vol.115, p.12186950, 2002.

J. D. Higgins, S. J. Armstrong, F. Franklin, and G. H. Jones, The Arabidopsis MutS homolog AtMSH4 functions at an early step in recombination: evidence for two classes of recombination in Arabidopsis, Genes Dev, vol.18, p.15489296, 2004.

P. E. Stronghill, W. Azimi, and C. A. Hasenkampf, A novel method to follow meiotic progression in Arabidopsis using confocal microscopy and 5-ethynyl-2 0-deoxyuridine labeling, Plant Methods, vol.10, p.25337148, 2014.