Skip to main content
Log in

Genetic relationships within Brassica rapa as inferred from AFLP fingerprints

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

Abstract

Amplified fragment length polymorphism (AFLP) markers were employed to assess the genetic diversity amongst two large collections of Brassica rapa accessions. Collection A consisted of 161 B. rapa accessions representing different morphotypes among the cultivated B. rapa, including traditional and modern cultivars and breeding materials from geographical locations from all over the world and two Brassica napus accessions. Collection B consisted of 96 accessions, representing mainly leafy vegetable types cultivated in China. On the basis of the AFLP data obtained, we constructed phenetic trees using mega 2.1 software. The level of polymorphism was very high, and it was evident that the amount of genetic variation present within the groups was often comparable to the variation between the different cultivar groups. Cluster analysis revealed groups, often with low bootstrap values, which coincided with cultivar groups. The most interesting information revealed by the phenetic trees was that different morphotypes are often more related to other morphotypes from the same region (East Asia vs. Europe) than to similar morphotypes from different regions, suggesting either an independent origin and or a long and separate domestication and breeding history in both regions.

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

Similar content being viewed by others

References

  • Bai Y, Huang CC, Hulst RGM van der, Dekens RG, Bonnema AB, Lindhout WH (2003) QTLs for tomato powdery mildew resistance (Oidium lycopersici) in Lycopersicon parviflorum G1.1601 colocalize with two qualitative powdery mildew resistance genes. Mol Plant Microbe Interact 16:169–176

    Google Scholar 

  • Cao JSh, Cao ShCh, Miao Y, Lu G (1997) Cladistic operational analysis and study on the evolution of Chinese cabbage groups (Brassica campestris L.). Acta Hortic Sin 24:35–42

    Google Scholar 

  • Chen YP, Cao JSh, Miao Y, Ye WZ (2000) Analysis of genetic polymorphism in vegetable crops of Brassica campestris by RAPD markers. J Zhejiang Univ (Agric Life Sci) 26:131–136

    Google Scholar 

  • Das S, Rajagopal J, Bhatia S, Srivastava PS, Lakshmikumaran M (1999) Assessment of genetic variation within Brassica campestris cultivars using amplified fragment length polymorphism and random amplification of polymorphic DNA markers. J Biosci 24:433–440

    Google Scholar 

  • Demeke T, Adams RP, Chibbar R (1992) Potential taxonomic use of random amplified polymorphic DNA (RAPD): a case study in Brassica. Theor Appl Genet 84:990–994

    Google Scholar 

  • Diederichsen A (2001) Brassica rapa group. In: Hanelt P (ed) Mansfelds encyclopedia of agricultural and horticultural crops (except ornamentals). Springer, Berlin Heidelberg New York, pp 1446–1453

  • Gomez Campo C (1999) Developments in plant genetics and breeding, vol 4. Biology of Brassica coenospecies. Elsevier, Amsterdam Lausanne New York Oxford Shannon Singapore Tokyo

    Google Scholar 

  • Guo JX, Zhou NY, Ma RC, Cao MQ (2002) Genetic diversity in Brassica rapa revealed by AFLP molecular markers. J Agric Biotechnol 10:138–143

    Google Scholar 

  • He YT, Tu JX, Fu TD, Li DR, Chen BY (2002) Genetic diversity of germplasm resources of Brassica campestris L. in China by RAPD markers. Acta Agron Sin 28:697–703

    Google Scholar 

  • He YT, Chen BY, Fu TD, Li DR, TU JX (2003) Origins and evolution of Brassica campestris L. in China. Acta Genet Sin 30:1003–1012

    Google Scholar 

  • Huang JCh, Corke H, Sun M (2002) Highly polymorphic AFLP markers as a complementary tool to ITS sequences in assessing genetic diversity and phylogenetic relationships of sweetpotato (Ipomoea batatas (L.) Lam.) and its wild relatives. Genet Resour Crop Evol 49:541–550

    Google Scholar 

  • Jain A, Bhatia S, Banga SS, Prakash S, Lakshmikumaran M (1994) Potential use of random amplified polymorphic DNA (RAPD) technique to study the genetic diversity in Indian mustard (Brassica juncea) and its relationship to heterosis. Theor Appl Genet 88:116–122

    Google Scholar 

  • Koopman WJM, Zevenbergen MJ, Van den Berg RG (2001) Species relationships in Lactuca SL. (Lactuceae, Asteraceae) inferred from AFLP fingerprints. Am J Bot 88:1881–1887

    Google Scholar 

  • Kumar S, Tamura K, Jakobsen IB, Nei M (2001) mega2: molecular evolutionary genetics analysis software. Arizona State University, Tempe, Arizona

    Google Scholar 

  • Li JW (1981) The origins and evolution of vegetable crops in China. Sci Agric Sin 14:90–95

    Google Scholar 

  • Liu HL (1984) Origin and evolution of genus Brassica oilseed rapes. Acta Agron Sin 10:9–18

    Google Scholar 

  • Mackill DJ, Zhang Z, Redona ED, Colowit PM (1996) Level of polymorphism and genetic mapping of AFLP markers in rice. Genome 39:969–977

    CAS  PubMed  Google Scholar 

  • Mizushima V (1980) Genome analysis in Brassica and allied genera. In: Tsunoda S, Hinata K, Gomez-Campo C (eds) Brassica crops and wild allies. Japan Scientific Societies Press, Tokyo, pp 89–105

    Google Scholar 

  • Myburg AA, Remington DL (2000) Protocol for high-throughput AFLP analysis using LI-COR IR2 automated sequencer. North Carolina State Forest Biotechnology AFLP protocol. N C State Univ For Dep, Raleigh N.C.

    Google Scholar 

  • Negi MS, Sabharwal V, Bhat SR, Lakshmikumaran M (2004) Utility of AFLP markers for the assessment of genetic diversity within Brassica nigra germplasm. Plant Breed 123:13–16

    Google Scholar 

  • Powell W, Morgante M, Andre C, Hanafey M, Vogel J, Tingey S, Rafalaski A (1996) The comparison of RFLP, RAPD, AFLP and SSR (microsatellite) markers for germplasm analysis. Mol Breed 3:225–238

    Google Scholar 

  • Prakash S, Hinata K (1980) Taxonomy, cytogenetics and origin of crop Brassica, a review. Opera Bot 55:1–57

    Google Scholar 

  • Reiner H, Holzner W, Ebermann R (1995) The development of turnip-type and oilseed-type Brassica rapa crops from wild-type in Europe—an overview of botanical, historical and linguistic facts. Rapeseed Today Tomorrow 4:1066–1069

    Google Scholar 

  • Siemonsma JS, Piluek K (1993) Plant resources of south-east Asia, no. 8. Vegetables. Pudoc, Wageningen, pp 121–134

    Google Scholar 

  • Song KM, Osborn TC, Williams PH (1988a) Brassica taxonomy based on nuclear restriction fragment length polymorphism (RFLPs). 1. Genome evolution of diploid and amphidiploid species. Theor Appl Genet 75:784–794

    CAS  Google Scholar 

  • Song KM, Osborn TC, Williams PH (1988b) Brassica taxonomy based on nuclear restriction fragment length polymorphism (RFLPs). 2. Preliminary analysis of sub-species within B. rapa (syn campestris) and B. oleracea. Theor Appl Genet 76:593–600

    Google Scholar 

  • Song KM, Osborn TC, Williams PH (1990) Brassica taxonomy based on nuclear restriction fragment length polymorphisms (RFLPs) 3. Genome relationships in Brassica and related genera and the origin of B. oleracea and B. rapa (syn. campestris). Theor Appl Genet 76:497–506

    Google Scholar 

  • Srivastava A, Gupta V, Pental D, Pradhan AK (2001) AFLP-based genetic diversity assessment amongst agronomically important natural and some newly synthesized lines of Brassica juncea. Theor Appl Genet 102:193–99

    Google Scholar 

  • Thormann CE, Ferreira ME, Carmago LEA, Tivang JG, Osborn TC (1994) Comparison of RFLP and RAPD markers to estimate genetic relationships within and among cruciferous species. Theor Appl Genet 88:973–980

    Google Scholar 

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

    Google Scholar 

  • Van der Beek JG, Verkerk R, Zabel P, Lindhout P (1992) Mapping strategy for resistance genes in tomato based on RFLPs between cultivars: Cf9 (resistance to Cladosporium fulvum) on chromosome 1. Theor Appl Genet 84:106–112

    Google Scholar 

  • Vaughan JG (1977) A multidisciplinary study of the taxonomy and origin of Brassica crops. Bioscience 27:35–40

    Google Scholar 

  • Vos P, Hogers R, Bleeker M, Rijan M, van der Lee T, Hornes M, Frijters A, Pot J, Peleman J, Kuiper M, Zabeau M (1995) AFLP: a new technique for DNA fingerprinting. Nucleic Acids Res 23:4407–4414

    CAS  PubMed  Google Scholar 

  • Williams PH, Hill CB (1986) Rapid cycling populations of Brassica. Science 232:1385–1389

    Google Scholar 

  • Zhu Y, Zheng Y (2001) Atlas of the traditional vegetables in China. Zhe Jiang Science and Technology Publishing House, China

    Google Scholar 

Download references

Acknowledgements

We thank P. van der Berg for technical support and the Wageningen Plant Sciences Experimental Centre of Wageningen University for taking care of the plants. We thank Noortje Bas from the Centre for Genetic Resources The Netherlands (CGN) Wageningen-UR, Li XiXiang from the Institute of Vegetables and Flowers, Chinese Academy of Agricultural Sciences and Xu Zeyong, Oil Crop Research Institute, Chinese Academy of Agricultural Sciences, for kindly supplying the accessions used in this study. This project is sponsored by the Asian Facility (project AF01/CH/8 “Sino-Dutch Genomic Lab and Vegetable Research Center”).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Guusje Bonnema.

Additional information

Communicated by H.C. Becker

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zhao, J., Wang, X., Deng, B. et al. Genetic relationships within Brassica rapa as inferred from AFLP fingerprints. Theor Appl Genet 110, 1301–1314 (2005). https://doi.org/10.1007/s00122-005-1967-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00122-005-1967-y

Keywords

Navigation