Skip to main content
Log in

Pairing and recombination at meiosis of Brassica rapa (AA) × Brassica napus (AACC) hybrids

  • Original Paper
  • Published:
Theoretical and Applied Genetics Aims and scope Submit manuscript

Abstract

Interspecific crosses contribute significantly to plant evolution enabling gene exchanges between species. The efficiency of interspecific crosses depends on the similarity between the implicated genomes as high levels of genome similarity are required to ensure appropriate chromosome pairing and genetic recombination. Brassica napus (AACC) is an allopolyploid, resulting from natural hybridization between Brassica rapa (AA) and Brassica oleracea (CC), both being diploid species derived from a common ancestor. To study the relationships between genomes of these Brassica species, we have determined simultaneously the pairing and recombination pattern of A and C chromosomes during meiosis of AAC triploid hybrids, which result from the interspecific cross between natural B. napus and B. rapa. Different AAC triploid hybrids and their progenies have been analysed using cytogenetic, BAC-FISH, and molecular techniques. In 71% of the pollen mother cells, homologous A chromosomes paired regularly, and usually one chromosome of each pair was transmitted to the progeny. C chromosomes remained mainly univalent, but were involved in homoeologous pairing in 21.5% of the cells, and 13% of the transmitted C chromosomes were either recombined or broken. The rate of transmission of C chromosomes depended on the identity of the particular chromosome and on the way the hybrid was crossed, as the male or as the female parent, to B. napus or to B. rapa. Gene transfers in triploid hybrids are favoured between A genomes of B. rapa and B. napus, but also occur between A and C genomes though at lower rates.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  • Armstrong KC, Keller WA (1982) Chromosome pairing in haploids of Brassica oleracea. Can J Genet Cytol 24:735–739

    Google Scholar 

  • Armstrong SJ, Caryl AP, Jones GH, Franklin FCH (2002) Asy1, a protein required for melotic chromosome synapsis, localizes to axis-associated chromatin in Arabidopsis and Brassica. J Cell Sci 115:3645–3655

    Article  PubMed  CAS  Google Scholar 

  • Attia T, Busso C, Röbbelen G (1987) Digenomic triploids for an assessment of chromosome relationships in the cultivated diploid Brassica species. Genome 29:326–330

    Google Scholar 

  • Attia T, Röbbelen G (1986) Cytogenetic relationship within cultivated Brassica analyzed in amphihaploids from the three diploid ancestors. Can J Genet Cytol 28:323–329

    Google Scholar 

  • Boudry P, Morchen M, Saumitoulaprade P, Vernet P, Vandijk H (1993) The origin and evolution of weed beets—consequences for the breeding and release of herbicide-resistant transgenic sugar-beets. Theor Appl Genet 87:471–478

    Article  Google Scholar 

  • Chen BY, Heneen WK, Simonsen V (1990) Genetics of isozyme loci in Brassica campestris L. and in the progeny of a trigenomic hybrid between B. napus L. and B. campestris L. Genome 33:433–440

    CAS  Google Scholar 

  • Chen BY, Simonsen V, Lannerherrera C, Heneen WK (1992) A Brassica campestris-alboglabra addition line and its use for gene-mapping, intergenomic gene-transfer and generation of trisomics. Theor Appl Genet 84:592–599

    Google Scholar 

  • Cheng BF, Heneen WK, Chen BY (1994) Meiotic studies on a Brassica campestris-alboglabra monosomic addition line and derived Brassica campestris primary trisomics. Genome 37:584–589

    Google Scholar 

  • Doyle JJ, Doyle JL (1990) Isolation of plant DNA from fresh tissue. Focus 12:13–15

    Google Scholar 

  • Eber F, Letanneur JC, Chèvre AM (1997) Chromosome number of oilseed rape (Brassica napus)-wild radish (Raphanus raphanistrum) spontaneous hybrids and of their progeny estimated by flow cytometry. Cruciferae Newsl 19:17–18

    Google Scholar 

  • Ellstrand NC, Prentice HC, Hancock JF (1999) Gene flow and introgression from domesticated plants into their wild relatives. Annu Rev Ecol Syst 30:539–563

    Article  Google Scholar 

  • Fantes JA, MacKay GR (1979) The production of disomic addition lines of Brassica campestris. Eucarpia Cruciferae Newsl 4:36–37

    Google Scholar 

  • Foisset N, Delourme R, Barret P, Hubert N, Landry BS, Renard M (1996) Molecular-mapping analysis in Brassica napus using isozyme, RAPD and RFLP markers on a doubled haploid progeny. Theor Appl Genet 93:1017–1025

    Article  CAS  Google Scholar 

  • Frankel OM, Brown AHD, Burdon JJ (1995) The conservation of plant biodiversity, vol, edn. Cambridge University Press, Cambridge

  • Friebe B, Zhang P, Linc G, Gill BS (2005) Robertsonian translocations in wheat arise by centric misdivision of univalents at anaphase I and rejoining of broken centromeres during interkinesis of meiosis II. Cytogenet Genome Res 109:293–297

    Article  PubMed  CAS  Google Scholar 

  • Hasterok R, Wolny E, Kulak S, Zdziechiewicz A, Maluszynska J, Heneen WK (2005) Molecular cytogenetic analysis of Brassica rapa-Brassica oleracea var. alboglabra monosomic addition lines. Theor Appl Genet 111:196–205

    Article  PubMed  CAS  Google Scholar 

  • Heneen WK, Chen BY, Cheng BF, Jonsson A, Simonsen V, Jorgensen RB, Davik J (1995) Characterization of the A and C genomes of Brassica campestris and B. alboglabra. Hereditas 123:251–267

    Article  Google Scholar 

  • Heneen WK, Jorgensen RB (2001) Cytology, RAPD, and seed colour of progeny plants from Brassica rapa-alboglabra aneuploids and development of monosomic addition lines. Genome 44:1007–1021

    Article  PubMed  CAS  Google Scholar 

  • Higgins JD, Sanchez-Moran E, Armstrong SJ, Jones GH, Franklin FCH (2005) The Arabidopsis synaptonemal complex protein ZYP1 is required for chromosome synapsis and normal fidelity of crossing over. Genes Dev 19:2488–2500

    Article  PubMed  CAS  Google Scholar 

  • Howell EC, Barker GC, Jones GH, Kearsey MJ, King GJ, Kop EP, Ryder CD, Teakle GR, Vicente JG, Armstrong SJ (2002) Integration of the cytogenetic and genetic linkage maps of Brassica oleracea. Genetics 161:1225–1234

    PubMed  CAS  Google Scholar 

  • Inomata N (1980) Hybrid progenies of the cross, Brassica campestris x B. oleracea. I. Cytogenetical studies on F1 hybrids. Jap J Genet 55:189–202

    Google Scholar 

  • Jenczewski E, Eber F, Grimaud A, Huet S, Lucas MO, Monod H, Chèvre AM (2003) PrBn, a major gene controlling homoeologous pairing in oilseed rape (Brassica napus) haploids. Genetics 164:645–653

  • Johnston SA, Den Nijs TPM, Peloquin SJ, Hanneman RE (1980) The significance of genic balance to endosperm development in interspecific crosses. Theor Appl Genet 57:5–9

    Google Scholar 

  • Lagercrantz U, Lydiate DJ (1996) Comparative genome mapping in Brassica. Genetics 144:1903–1910

    PubMed  CAS  Google Scholar 

  • Lee KH, Namai H (1992) Pollen fertility and seed set percentage after backcrossing of sesquidiploids (AAC genomes) derived from interspecific hybrid between Brassica campestris L (AA) and Brassica oleracea L (CC) and frequency-distribution of aneuploids in the progenies. Jap J Breed 42:43–53

    Google Scholar 

  • Lu CM, Kato M (2001) Fertilization fitness and relation to chromosome number in interspecific progeny between Brassica napus and B. rapa: a comparative study using natural and resynthesized B. napus. Breed Sci 51:73–81

    Article  Google Scholar 

  • MacGrath JM, Quiros CF (1990) Generation of alien chromosome addition lines from synthetic Brassica napus: morphology, cytology, fertility and chromosome transmission. Genome 33:374–383

    Google Scholar 

  • MacKay GR (1977) The introgression of S alleles into forage rape, Brassica napus L. from turnip, Brassica campestris L. ssp. rapifera. Euphytica 26:511–519

    Article  Google Scholar 

  • MacNaughton IH (1973) Brassica napocampestris L. (2n = 58). 1. Synthesis, cytology, fertility and general considerations. Euphytica 22:301–309

    Article  Google Scholar 

  • Metz PLJ, Jacobsen E, Nap JP, Pereira A, Stiekema WJ (1997) The impact on biosafety of the phosphinothricin-tolerance transgene in inter-specific B. rapa x B. napus hybrids and their successive backcrosses. Theor Appl Genet 95:442–450

    Article  CAS  Google Scholar 

  • Mikkelsen TR, Jensen J, Jorgensen RB (1996) Inheritance of oilseed rape (Brassica napus) RAPD markers in a backcross progeny with Brassica campestris. Theor Appl Genet 92:492–497

    Article  Google Scholar 

  • Namai H (1987) Inducing cytogenetical alterations by means of interspecific and intergeneric hybridization in Brassica crops. Gamma Field Symp 26:41–89

    Google Scholar 

  • Panestos CA, Baker H (1967) The origin of variation in « wild » Raphanus sativus in California. Genetica 38:243–274

    Article  Google Scholar 

  • Parkin IAP, Gulden SM, Sharpe AG, Lukens L, Trick M, Osborn TC, Lydiate DJ (2005) Segmental structure of the Brassica napus genome based on comparative analysis with Arabidopsis thaliana. Genetics 171:765–781

    Article  PubMed  CAS  Google Scholar 

  • Parkin IAP, Sharpe AG, Keith DJ, Lydiate DJ (1995) Identification of the A and C genomes of amphidiploid Brassica napus (oilseed rape). Genome 38:1122–1131

    CAS  Google Scholar 

  • Parkin IAP, Sharpe AG, Lydiate DJ (2003) Patterns of genome duplication within the Brassica napus genome. Genome 46:291–303

    Article  PubMed  CAS  Google Scholar 

  • Prieto JL, Pouilly N, Jenczewski E, Deragon JM, Chevre AM (2005) Development of crop-specific transposable element (SINE) markers for studying gene flow from oilseed rape to wild radish. Theor Appl Genet 111:446–455

    Article  PubMed  CAS  Google Scholar 

  • Quiros CF, Ochoa O, Kianan SF, Douches D (1987) Analysis of the Brassica oleracea genome by the generation of B. campestris-oleracea chromosome addition lines: characterization by isozymes and rDNA genes. Theor Appl Genet 74:758–766

    CAS  Google Scholar 

  • Ramsey J, Schemske DW (2002) Neopolyploidy in flowering plants. Annu Rev Ecol Syst 33:589–639

    Article  Google Scholar 

  • Teutonico RA, Osborn TC (1994) Mapping of RFLP and qualitative trait loci in Brassica rapa and comparison to the linkage maps of Brassica napus, Brassica oleracea, and Arabidopsis thaliana. Theor Appl Genet 89:885–894

    Article  CAS  Google Scholar 

  • Tomiuk J, Hauser TP, Bagger-Jorgensen R (2000) A- or C-chromosomes, does it matter for the transfer of transgenes from Brassica napus. Theor Appl Genet 100:750–754

    Article  Google Scholar 

  • Truco MJ, Hu J, Sadowski J, Quiros CF (1996) Inter- and intra-genomic homology of the Brassica genomes: implications for their origin and evolution. Theor Appl Genet 93:1225–1233

    Article  CAS  Google Scholar 

  • U N (1935) Genome analysis in Brassica with special reference to the experimental formation of B. napus and peculiar mode of fertilization. Jpn J Bot 7:389–452

    Google Scholar 

  • Udall JA, Quijada PA, Osborn TC (2005) Detection of chromosomal rearrangements derived from homeologous recombination in four mapping populations of Brassica napus L. Genetics 169:967–979

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

Our colleagues of OUEST-Génopole® (Le Rheu, France) are gratefully acknowledged for their technical assistance. We thank B. Chalhoub and H. Belcram (URGV Evry, France) for providing PFM and the BAC 54B2, T. Ksiazczyk and J. Maluszynska (University of Silesia, Katowice, Poland) for providing a stab of BoBO14O06, R. Delourme (INRA Rennes, France) for Brassica mapping data and review of the paper, and M. Barbetti (University of Western Australia) for his critical reading of the manuscript. This work was funded by INRA, CETIOM and ANR Biodiversité.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to A. M. Chèvre.

Additional information

Communicated by B. Friebe.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Leflon, M., Eber, F., Letanneur, J.C. et al. Pairing and recombination at meiosis of Brassica rapa (AA) × Brassica napus (AACC) hybrids. Theor Appl Genet 113, 1467–1480 (2006). https://doi.org/10.1007/s00122-006-0393-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00122-006-0393-0

Keywords

Navigation