U. Abdu, A. Gonzalez-reyes, A. Ghabrial, and T. Schupbach, The Drosophila spn-D gene encodes a RAD51C-like protein that is required exclusively during meiosis, Genetics, vol.165, pp.197-204, 2003.

K. Abe, K. Osakabe, S. Nakayama, M. Endo, A. Tagiri et al., Arabidopsis RAD51C gene is important for homologous recombination in meiosis and mitosis, Plant Physiol, vol.139, pp.896-908, 2005.

S. Badie, C. Liao, M. Thanasoula, P. Barber, M. A. Hill et al., RAD51C facilitates checkpoint signaling by promoting CHK2 phosphorylation, J. Cell Biol, vol.185, pp.587-600, 2009.

D. K. Bishop and D. Zickler, Early decision; meiotic crossover interference prior to stable strand exchange and synapsis, Cell, vol.117, pp.9-15, 2004.

D. K. Bishop, U. Ear, A. Bhattacharyya, C. Calderone, M. Beckett et al., Xrcc3 is required for assembly of Rad51 complexes in vivo, J. Biol. Chem, vol.273, pp.21482-21488, 1998.

J. Y. Bleuyard and C. I. White, The Arabidopsis homologue of Xrcc3 plays an essential role in meiosis, EMBO J, vol.23, pp.439-449, 2004.
URL : https://hal.archives-ouvertes.fr/inserm-00595813

J. Y. Bleuyard, M. E. Gallego, and C. I. White, The atspo11-1 mutation rescues atxrcc3 meiotic chromosome fragmentation, Plant Mol. Biol, vol.56, pp.217-224, 2004.
URL : https://hal.archives-ouvertes.fr/inserm-00595809

J. Y. Bleuyard, M. E. Gallego, F. Savigny, and C. I. White, Differing requirements for the Arabidopsis Rad51 paralogs in meiosis and DNA repair, Plant J, vol.41, pp.533-545, 2005.
URL : https://hal.archives-ouvertes.fr/inserm-00595808

J. Y. Bleuyard, M. E. Gallego, and C. I. White, Recent advances in understanding of the DNA double-strand break repair machinery of plants, DNA Repair (Amst), vol.5, pp.1-12, 2006.
URL : https://hal.archives-ouvertes.fr/inserm-00595807

G. V. Borner, N. Kleckner, and N. Hunter, Crossover/noncrossover differentiation, synaptonemal complex formation, and regulatory surveillance at the leptotene/zygotene transition of meiosis, Cell, vol.117, pp.29-45, 2004.

V. Busygina, M. G. Sehorn, I. Y. Shi, H. Tsubouchi, G. S. Roeder et al., Hed1 regulates Rad51-mediated recombination via a novel mechanism, Genes Dev, vol.22, pp.786-795, 2008.

V. Busygina, D. Saro, G. Williams, W. K. Leung, A. F. Say et al., Novel attributes of Hed1 affect dynamics and activity of the Rad51 presynaptic filament during meiotic recombination, J. Biol. Chem, vol.287, pp.1566-1575, 2012.

J. A. Carballo, A. L. Johnson, S. G. Sedgwick, and R. S. Cha, Phosphorylation of the axial element protein Hop1 by Mec1/Tel1 ensures meiotic interhomolog recombination, Cell, vol.132, pp.758-770, 2008.

R. Cartwright, A. M. Dunn, P. J. Simpson, C. E. Tambini, and J. Thacker, Isolation of novel human and mouse genes of the recA/ RAD51 recombination-repair gene family, Nucleic Acids Res, vol.26, pp.1653-1659, 1998.

R. Cartwright, C. E. Tambini, P. J. Simpson, and J. Thacker, The XRCC2 DNA repair gene from human and mouse encodes a novel member of the recA/RAD51 family, Nucleic Acids Res, vol.26, pp.3084-3089, 1998.

C. Charbonnel, M. E. Gallego, and C. I. White, Xrcc1-dependent and Ku-dependent DNA double-strand break repair kinetics in Arabidopsis plants, Plant J, vol.64, pp.280-290, 2010.
URL : https://hal.archives-ouvertes.fr/inserm-00595784

C. Charbonnel, E. Allain, M. E. Gallego, and C. I. White, Kinetic analysis of DNA double-strand break repair pathways in Arabidopsis, DNA Repair (Amst.), vol.10, pp.611-619, 2011.
URL : https://hal.archives-ouvertes.fr/inserm-00595841

J. Chun, E. S. Buechelmaier, and S. N. Powell, The Rad51 paralog complexes BCDX2 and CX3 act at different stages in the BRCA1-BRCA2 dependent homologous recombination pathway, Mol. Cell. Biol, vol.33, pp.387-395, 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, pp.1222-1225, 2012.

F. Cole, L. Kauppi, J. Lange, I. Roig, R. Wang et al., Homeostatic control of recombination is implemented progressively in mouse meiosis, Nat. Cell Biol, vol.14, pp.424-430, 2012.

S. A. Compton, S. Ozgur, and J. D. Griffith, Ring-shaped Rad51 paralog protein complexes bind Holliday junctions and replication forks as visualized by electron microscopy, J. Biol. Chem, vol.285, pp.13349-13356, 2010.

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, pp.1623-1634, 1999.

W. Crismani, C. Girard, N. Froger, M. Pradillo, J. L. Santos et al., FANCM limits meiotic crossovers, Science, vol.336, pp.1588-1590, 2012.
URL : https://hal.archives-ouvertes.fr/hal-01004174

W. Crismani, V. Portemer, N. Froger, L. Chelysheva, C. Horlow et al., MCM8 Is required for a pathway of meiotic double-strand break repair independent of DMC1 in Arabidopsis thaliana, PLoS Genet, vol.9, p.1003165, 2013.
URL : https://hal.archives-ouvertes.fr/hal-01190669

O. Da-ines, K. Abe, C. Goubely, M. E. Gallego, and C. I. White, Differing requirements for RAD51 and DMC1 in meiotic pairing of centromeres and chromosome arms in Arabidopsis thaliana, PLoS Genet, vol.8, p.1002636, 2012.
URL : https://hal.archives-ouvertes.fr/inserm-01907402

A. De-muyt, L. Jessop, E. Kolar, A. Sourirajan, J. Chen et al., BLM helicase ortholog Sgs1 is a central regulator of meiotic recombination intermediate metabolism, Mol. Cell, vol.46, pp.43-53, 2012.

W. E. Durrant, S. Wang, and X. Dong, Arabidopsis SNI1 and RAD51D regulate both gene transcription and DNA recombination during the defense response, Proc. Natl Acad. Sci. USA, vol.104, pp.4223-4227, 2007.

M. Ferdous, J. D. Higgins, and K. Osman, Inter-homolog crossingover and synapsis in Arabidopsis meiosis are dependent on the chromosome axis protein AtASY3, PLoS Genet, vol.8, p.1002507, 2012.

K. E. Francis, S. Y. Lam, B. D. Harrison, A. L. Bey, L. E. Berchowitz et al., Pollen tetrad-based visual assay for meiotic recombination in Arabidopsis, Proc. Natl Acad. Sci. USA, vol.104, pp.3913-3918, 2007.

J. D. Friesner, B. Liu, K. Culligan, and A. B. Britt, Ionizing radiationdependent gamma-H2AX focus formation requires ataxia telangiectasia mutated and ataxia telangiectasia mutated and Rad3-related, Mol. Biol. Cell, vol.16, pp.2566-2576, 2005.

S. L. Gasior, A. K. Wong, Y. Kora, A. Shinohara, and D. K. Bishop, Rad52 associates with RPA and functions with rad55 and rad57 to assemble meiotic recombination complexes, Genes Dev, vol.12, pp.2208-2221, 1998.

S. L. Gasior, H. Olivares, U. Ear, D. M. Hari, R. Weichselbaum et al., Assembly of RecA-like recombinases: distinct roles for mediator proteins in mitosis and meiosis, Proc. Natl Acad. Sci. USA, vol.98, pp.8411-8418, 2001.

A. Ghabrial, R. P. Ray, and T. Schupbach, ) okra and spindle-B encode components of the RAD52 DNA repair pathway and affect meiosis and patterning in Drosophila oogenesis, Genes Dev, vol.12, pp.2711-2723, 1998.

H. Gherbi, M. E. Gallego, N. Jalut, J. M. Lucht, B. Hohn et al., Homologous recombination in planta is stimulated in the absence of Rad50, EMBO Rep, vol.2, pp.287-291, 2001.
URL : https://hal.archives-ouvertes.fr/inserm-00595833

T. Goldfarb and M. Lichten, Frequent and efficient use of the sister chromatid for DNA double-strand break repair during budding yeast meiosis, PLoS Biol, vol.8, 2010.

W. D. Heyer, K. T. Ehmsen, and J. Liu, Regulation of homologous recombination in eukaryotes, Annu. Rev. Genet, vol.44, pp.113-139, 2010.

H. C. Ho and S. M. Burgess, Pch2 acts through Xrs2 and Tel1/ATM to modulate interhomolog bias and checkpoint function during meiosis, PLoS Genet, vol.7, p.1002351, 2011.

W. K. Holloman, Unraveling the mechanism of BRCA2 in homologous recombination, Nat. Struct. Mol. Biol, vol.18, pp.748-754, 2011.

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, pp.59-70, 2001.

R. W. Hyppa and G. R. Smith, Crossover invariance determined by partner choice for meiotic DNA break repair, Cell, vol.142, pp.243-255, 2010.

S. Inagaki, K. Nakamura, and A. Morikami, A link among DNA replication, recombination, and gene expression revealed by genetic and genomic analysis of TEBICHI gene of Arabidopsis thaliana, PLoS Genet, vol.5, p.1000613, 2009.

A. Knoll, J. D. Higgins, K. Seeliger, S. J. Reha, N. J. Dangel et al., The Fanconi anemia ortholog FANCM ensures ordered homologous recombination in both somatic and meiotic cells in Arabidopsis, Plant Cell, vol.24, pp.1448-1464, 2012.

B. O. Krogh and L. S. Symington, Recombination proteins in yeast, Annu. Rev. Genet, vol.38, pp.233-271, 2004.

M. T. Kurzbauer, C. Uanschou, D. Chen, and P. Schlogelhofer, The recombinases DMC1 and RAD51 are functionally and spatially separated during meiosis in Arabidopsis, Plant Cell, vol.24, pp.2058-2070, 2012.

S. Kuznetsov, M. Pellegrini, and K. Shuda, RAD51C deficiency in mice results in early prophase I arrest in males and sister chromatid separation at metaphase II in females, J. Cell Biol, vol.176, pp.581-592, 2007.

J. Lange, J. Pan, F. Cole, M. P. Thelen, M. Jasin et al., ATM controls meiotic double-strand-break formation, Nature, vol.479, pp.237-240, 2011.

W. Li and H. Ma, Double-stranded DNA breaks and gene functions in recombination and meiosis, Cell Res, vol.16, pp.402-412, 2006.

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. USA, vol.101, pp.10596-10601, 2004.

W. Li, X. Yang, Z. Lin, L. Timofejeva, R. Xiao et al., The AtRAD51C gene is required for normal meiotic chromosome synapsis and double-stranded break repair in Arabidopsis, Plant Physiol, vol.138, pp.965-976, 2005.

M. Lisby, J. H. Barlow, R. C. Burgess, and R. Rothstein, Choreography of the DNA damage response: spatiotemporal relationships among checkpoint and repair proteins, Cell, vol.118, pp.699-713, 2004.

Y. Liu, J. Y. Masson, R. Shah, P. O'regan, and S. C. West, RAD51C is required for Holliday junction processing in mammalian cells, Science, vol.303, pp.243-246, 2004.

Y. Liu, M. Tarsounas, P. O'regan, and S. C. West, Role of RAD51C and XRCC3 in genetic recombination and DNA repair, J. Biol. Chem, vol.282, pp.1973-1979, 2007.

J. Liu, L. Renault, X. Veaute, F. Fabre, H. Stahlberg et al., Rad51 paralogues Rad55-Rad57 balance the antirecombinase Srs2 in Rad51 filament formation, Nature, vol.479, pp.245-248, 2011.
URL : https://hal.archives-ouvertes.fr/cea-00881580

E. Lopez, M. Pradillo, C. Oliver, C. Romero, N. Cunado et al., Looking for natural variation in chiasma frequency in Arabidopsis thaliana, J. Exp. Bot, vol.63, pp.887-894, 2012.

A. Lorenz, F. Osman, W. Sun, S. Nandi, R. Steinacher et al., The fission yeast FANCM ortholog directs non-crossover recombination during meiosis, Science, vol.336, pp.1585-1588, 2012.

E. Martini, R. L. Diaz, N. Hunter, and S. Keeney, Crossover homeostasis in yeast meiosis, Cell, vol.126, pp.285-295, 2006.

C. Melamed-bessudo and A. A. Levy, Deficiency in DNA methylation increases meiotic crossover rates in euchromatic but not in heterochromatic regions in Arabidopsis, Proc. Natl Acad. Sci. USA, vol.109, pp.981-988, 2012.

C. Melamed-bessudo, E. Yehuda, A. R. Stuitje, and A. A. Levy, A new seed-based assay for meiotic recombination in Arabidopsis thaliana, Plant J, vol.43, pp.458-466, 2005.

R. Mercier, S. J. Armstrong, C. Horlow, N. P. Jackson, C. A. Makaroff et al., The meiotic protein SWI1 is required for axial element formation and recombination initiation in Arabidopsis, Development, vol.130, pp.3309-3318, 2003.

A. V. Nimonkar, C. C. Dombrowski, J. S. Siino, A. Z. Stasiak, A. Stasiak et al., Saccharomyces cerevisiae Dmc1 and Rad51 proteins preferentially function with Tid1 and Rad54 proteins, respectively, to promote DNA strand invasion during genetic recombination, J. Biol. Chem, vol.287, pp.28727-28737, 2012.

H. Niu, L. Wan, B. Baumgartner, D. Schaefer, J. Loidl et al., Partner choice during meiosis is regulated by Hop1promoted dimerization of Mek1, Mol. Biol. Cell, vol.16, pp.5804-5818, 2005.

S. D. Oh, J. P. Lao, P. Y. Hwang, A. F. Taylor, G. R. Smith et al., BLM ortholog, Sgs1, prevents aberrant crossing-over by suppressing formation of multichromatid joint molecules, Cell, vol.130, pp.259-272, 2007.

K. Osakabe, T. Yoshioka, H. Ichikawa, and S. Toki, Molecular cloning and characterization of RAD51-like genes from Arabidopsis thaliana, Plant Mol. Biol, vol.50, pp.71-81, 2002.

K. Osakabe, K. Abe, and H. Yamanouchi, Arabidopsis Rad51B is important for double-strand DNA breaks repair in somatic cells, Plant Mol. Biol, vol.57, pp.819-833, 2005.

K. Osman, J. D. Higgins, E. Sanchez-moran, S. J. Armstrong, and F. C. Franklin, Pathways to meiotic recombination in Arabidopsis thaliana, New Phytol, vol.190, pp.523-544, 2011.

J. Pan, M. Sasaki, and R. Kniewel, A hierarchical combination of factors shapes the genome-wide topography of yeast meiotic recombination initiation, Cell, vol.144, pp.719-731, 2011.

A. Pecinka, W. Fang, M. Rehmsmeier, A. A. Levy, and O. Scheid, Polyploidization increases meiotic recombination frequency in Arabidopsis, BMC Biol, vol.9, p.24, 2011.

M. Pradillo and J. L. Santos, The template choice decision in meiosis: is the sister important?, Chromosoma, vol.120, pp.447-454, 2011.

M. Pradillo, E. Lopez, R. Linacero, C. Romero, N. Cunado et al., Together yes, but not coupled: new insights into the roles of RAD51 and DMC1 in plant meiotic recombination, Plant J, vol.69, pp.921-933, 2012.

H. Puchta, P. Swoboda, S. Gal, M. Blot, and B. Hohn, Somatic intrachromosomal homologous recombination events in populations of plant siblings, Plant Mol. Biol, vol.28, pp.281-292, 1995.

Y. Qing, M. Yamazoe, K. Hirota, D. Dejsuphong, W. Sakai et al., The epistatic relationship between BRCA2 and the other RAD51 mediators in homologous recombination, PLoS Genet, vol.7, 2011.

A. Rodrigue, Y. Coulombe, K. Jacquet, J. P. Gagne, C. Roques et al., The RAD51 paralogs ensure cellular protection against mitotic defects and aneuploidy, J. Cell Sci, vol.126, pp.348-359, 2013.

S. Rosu, D. E. Libuda, and A. M. Villeneuve, Robust crossover assurance and regulated interhomolog access maintain meiotic crossover number, Science, vol.334, pp.1286-1289, 2011.

N. Roth, J. Klimesch, S. Dukowic-schulze, M. Pacher, A. Mannuss et al., The requirement for recombination factors differs considerably between different pathways of homologous double-strand break repair in somatic plant cells, Plant J, vol.72, pp.781-790, 2012.

J. San-filippo, P. Sung, and H. Klein, Mechanism of eukaryotic homologous recombination, Annu. Rev. Biochem, vol.77, pp.229-257, 2008.

E. Sanchez-moran, S. J. Armstrong, J. L. Santos, F. C. Franklin, and G. H. Jones, Variation in chiasma frequency among eight accessions of Arabidopsis thaliana, Genetics, vol.162, pp.1415-1422, 2002.

E. Sanchez-moran, J. L. Santos, G. H. Jones, and F. C. Franklin, ASY1 mediates AtDMC1-dependent interhomolog recombination during meiosis in Arabidopsis, Genes Dev, vol.21, pp.2220-2233, 2007.

A. Schwacha and N. Kleckner, Identification of joint molecules that form frequently between homologs but rarely between sister chromatids during yeast meiosis, Cell, vol.76, pp.51-63, 1994.

A. Schwacha and N. Kleckner, Interhomolog bias during meiotic recombination: meiotic functions promote a highly differentiated interhomolog-only pathway, Cell, vol.90, pp.1123-1135, 1997.
DOI : 10.1016/s0092-8674(00)80378-5
URL : https://doi.org/10.1016/s0092-8674(00)80378-5

K. Seeliger, S. Dukowic-schulze, R. Wurz-wildersinn, M. Pacher, and H. Puchta, BRCA2 is a mediator of RAD51-and DMC1-facilitated homologous recombination in Arabidopsis thaliana, New Phytol, vol.193, pp.364-375, 2012.

M. E. Serrentino and V. Borde, The spatial regulation of meiotic recombination hotspots: are all DSB hotspots crossover hotspots? Exp, Cell Res, vol.318, pp.1347-1352, 2012.

A. Sessions, E. Burke, and G. Presting, A high-throughput Arabidopsis reverse genetics system, Plant Cell, vol.14, pp.2985-2994, 2002.
DOI : 10.1105/tpc.004630
URL : http://www.plantcell.org/content/14/12/2985.full.pdf

N. Siaud, E. Dray, I. Gy, E. Gerard, N. Takvorian et al., Brca2 is involved in meiosis in Arabidopsis thaliana as suggested by its interaction with Dmc1, EMBO J, vol.23, pp.1392-1401, 2004.

P. G. Smiraldo, A. M. Gruver, J. C. Osborn, and D. L. Pittman, Extensive chromosomal instability in Rad51d-deficient mouse cells, Cancer Res, vol.65, pp.2089-2096, 2005.
DOI : 10.1158/0008-5472.can-04-2079
URL : http://cancerres.aacrjournals.org/content/65/6/2089.full.pdf

N. Suwaki, K. Klare, and M. Tarsounas, RAD51 paralogs: roles in DNA damage signalling, recombinational repair and tumorigenesis, Semin. Cell Dev. Biol, vol.22, pp.898-905, 2011.
DOI : 10.1016/j.semcdb.2011.07.019

P. Swoboda, S. Gal, B. Hohn, and H. Puchta, Intrachromosomal homologous recombination in whole plants, EMBO J, vol.13, pp.484-489, 1994.
DOI : 10.1002/j.1460-2075.1994.tb06283.x
URL : https://onlinelibrary.wiley.com/doi/pdf/10.1002/j.1460-2075.1994.tb06283.x

M. Takata, M. S. Sasaki, E. Sonoda, T. Fukushima, C. Morrison et al., The Rad51 paralog Rad51B promotes homologous recombinational repair, Mol. Cell. Biol, vol.20, pp.6476-6482, 2000.
DOI : 10.1128/mcb.20.17.6476-6482.2000
URL : https://mcb.asm.org/content/20/17/6476.full.pdf

M. Takata, M. S. Sasaki, S. Tachiiri, T. Fukushima, E. Sonoda et al., Chromosome instability and defective recombinational repair in knockout mutants of the five Rad51 paralogs, Mol. Cell. Biol, vol.21, pp.2858-2866, 2001.

C. E. Tambini, K. G. Spink, C. J. Ross, M. A. Hill, and J. Thacker, The importance of XRCC2 in RAD51-related DNA damage repair, DNA Repair (Amst.), vol.9, pp.517-525, 2010.

M. Tarsounas, A. A. Davies, and S. C. West, RAD51 localization and activation following DNA damage, Philos. Trans. R. Soc. Lond. B Biol. Sci, vol.359, pp.87-93, 2004.
DOI : 10.1098/rstb.2003.1368
URL : http://europepmc.org/articles/pmc1693300?pdf=render

M. Tarsounas, P. Munoz, A. Claas, P. G. Smiraldo, D. L. Pittman et al., Telomere maintenance requires the RAD51D recombination/repair protein, Cell, vol.117, pp.337-347, 2004.
DOI : 10.1016/s0092-8674(04)00337-x
URL : https://doi.org/10.1016/s0092-8674(04)00337-x

J. Thacker, The RAD51 gene family, genetic instability and cancer, Cancer Lett, vol.219, pp.125-135, 2005.
DOI : 10.1016/j.canlet.2004.08.018

H. Tsubouchi and G. S. Roeder, Budding yeast Hed1 down-regulates the mitotic recombination machinery when meiotic recombination is impaired, Genes Dev, vol.20, pp.1766-1775, 2006.
DOI : 10.1101/gad.1422506
URL : http://genesdev.cshlp.org/content/20/13/1766.full.pdf

L. R. Van-veelen, T. Cervelli, M. W. Van-de-rakt, A. F. Theil, J. Essers et al., Analysis of ionizing radiation-induced foci of DNA damage repair proteins, Mutat. Res, vol.574, pp.22-33, 2005.

L. R. Van-veelen, J. Essers, M. W. Van-de-rakt, H. Odijk, A. Pastink et al., Ionizing radiation-induced foci formation of mammalian Rad51 and Rad54 depends on the Rad51 paralogs, but not on Rad52, Mutat. Res, vol.574, pp.34-49, 2005.

J. Vignard, T. Siwiec, L. Chelysheva, N. Vrielynck, F. Gonord et al., The interplay of RecArelated proteins and the MND1-HOP2 complex during meiosis in Arabidopsis thaliana, PLoS Genet, vol.3, pp.1894-1906, 2007.

H. Yang, P. Lu, Y. Wang, and H. Ma, The transcriptome landscape of Arabidopsis male meiocytes from high-throughput sequencing: the complexity and evolution of the meiotic process, Plant J, vol.65, pp.503-516, 2011.

N. E. Yelina, K. Choi, and L. Chelysheva, Epigenetic remodeling of meiotic crossover frequency in Arabidopsis thaliana DNA methyltransferase mutants, PLoS Genet, vol.8, 2012.
URL : https://hal.archives-ouvertes.fr/hal-01190760

H. Yokoyama, H. Kurumizaka, S. Ikawa, S. Yokoyama, and T. Shibata, Holliday junction binding activity of the human Rad51B protein, J. Biol. Chem, vol.278, pp.2767-2772, 2003.

H. Yokoyama, N. Sarai, W. Kagawa, R. Enomoto, T. Shibata et al., Preferential binding to branched DNA strands and strand-annealing activity of the human Rad51B, Rad51C, Rad51D and Xrcc2 protein complex, Nucleic Acids Res, vol.32, pp.2556-2565, 2004.

Y. Yonetani, H. Hochegger, E. Sonoda, S. Shinya, H. Yoshikawa et al., Differential and collaborative actions of Rad51 paralog proteins in cellular response to DNA damage, Nucleic Acids Res, vol.33, pp.4544-4552, 2005.

J. L. Youds and S. J. Boulton, The choice in meiosis-defining the factors that influence crossover or non-crossover formation, J. Cell Sci, vol.124, pp.501-513, 2011.

J. L. Youds, D. G. Mets, M. J. Mcilwraith, J. S. Martin, J. D. Ward et al., RTEL-1 enforces meiotic crossover interference and homeostasis, Science, vol.327, pp.1254-1258, 2010.

K. Zakharyevich, S. Tang, Y. Ma, and N. Hunter, Delineation of joint molecule resolution pathways in meiosis identifies a crossover-specific resolvase, Cell, vol.149, pp.334-347, 2012.