Skip to main content
Log in

Chromosomal rearrangements differentiating the ryegrass genome from the Triticeae, oat, and rice genomes using common heterologous RFLP probes

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

Abstract

An restriction fragment length polymorphism (RFLP)-based genetic map of ryegrass (Lolium) was constructed for comparative mapping with other Poaceae species using heterologous anchor probes. The genetic map contained 120 RFLP markers from cDNA clones of barley (Hordeum vulgare L.), oat (Avena sativa L.), and rice (Oryza sativa L.), covering 664 cM on seven linkage groups (LGs). The genome comparisons of ryegrass relative to the Triticeae, oat, and rice extended the syntenic relationships among the species. Seven ryegrass linkage groups were represented by 10 syntenic segments of Triticeae chromosomes, 12 syntenic segments of oat chromosomes, or 16 syntenic segments of rice chromosomes, suggesting that the ryegrass genome has a high degree of genome conservation relative to the Triticeae, oat, and rice. Furthermore, we found ten large-scale chromosomal rearrangements that characterize the ryegrass genome. In detail, a chromosomal rearrangement was observed on ryegrass LG4 relative to the Triticeae, four rearrangements on ryegrass LGs2, 4, 5, and 6 relative to oat, and five rearrangements on ryegrass LGs1, 2, 4, 5, and 7 relative to rice. Of these, seven chromosomal rearrangements are reported for the first time in this study. The extended comparative relationships reported in this study facilitate the transfer of genetic knowledge from well-studied major cereal crops to ryegrass.

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

Similar content being viewed by others

References

  • Ahn SN, Tanksley SD (1993) Comparative linkage maps of the rice and maize genomes. Proc Natl Acad Sci USA 90:7980–7984

    CAS  PubMed  Google Scholar 

  • Alm V, Fang C, Busso CS, Devos KM, Vollan K, Grieg Z, Rognli OA (2003) A linkage map of meadow fescue (Festuca pratensis Huds.) and comparative mapping with other Poaceae species. Theor Appl Genet 108:25–40

    Article  CAS  PubMed  Google Scholar 

  • Bert PE, Charmet G, Sourdille P, Hayward MD, Balfourier F (1999) A high-density molecular map for ryegrass (Lolium perenne L.) using AFLP markers. Theor Appl Genet 99:445–452

    Article  CAS  Google Scholar 

  • Bonierbale M, Plaisted RL, Tanksley SD (1988) RFLP maps of potato and tomato based on a common set of clones reveal modes of chromosomal evolution. Genetics 120:1095–1103

    Google Scholar 

  • Castiglioni P, Pozzi C, Heun M, Terzi V, Muller KJ, Rohde W, Salamini F (1998) An AFLP-based procedure for the efficient mapping of mutations and DNA probes in barley. Genetics 149:2039–2056

    CAS  PubMed  Google Scholar 

  • Devos KM, Atkinson MD, Chinoy CN, Francis HA, Harcourt RL, Koebner RMD, Liu CJ, Masojc P, Xie DX, Gale MD (1993) Chromosomal rearrangements in the rye genome relative to that of wheat. Theor Appl Genet 85:673–680

    CAS  Google Scholar 

  • Devos KM, Chao S, Li QY, Simonetti MC, Gale M (1994) Relationship between chromosome 9 of maize and wheat homoeologous group 7 chromosomes. Genetics 138:1287–1292

    Google Scholar 

  • Dubcovsky J, Luo MC, Zhong GY, Bransteitter R, Desai A, Kilian A, Kleinhofs A, Dvorak J (1996) Genetic map of diploid wheat (Triticum monococcum L.) and its comparison with maps of Hordeum vulgare L. Genetics 143:983–999

    Google Scholar 

  • Francki M, Carter M, Ryan K, Hunter A, Bellgard M, Appels R (2004) Comparative organization of wheat homoeologous group 3S and 7L using wheat-rice synteny and identification of potential markers for genes controlling xanthophylls content in wheat. Funct Integr Genomics 4:118–130

    Article  CAS  PubMed  Google Scholar 

  • Gale MD, Devos KM (1997) Comparative genetics in the grasses. Plant Mol Biol 35:3–15

    Article  CAS  PubMed  Google Scholar 

  • Hayward MD, McAdam, NJ, Jones JG, Evans C, Evans GM, Forster JW, Ustin A, Hussain KG, Quader B, Stammers M, Will JAK (1994) Genetic markers and the selection of quantitative traits in forage grasses. Euphytica 77:269–275

    Google Scholar 

  • Hayward MD, Forster JW, Jones JG, Dolstra O, Evans C, McAdam NJ, Hossain KG, Stammers M, Will JAK, Humphreys MO, Evans GM (1998) Genetic analysis of Lolium. I. Identification of linkage groups and the establishment of a genetic map. Plant Breed 117:451–455

    Google Scholar 

  • Hulbert SH, Richter TE, Axtell JD, Bennetzen JL (1990) Genetic mapping and characterization of sorghum and related crops by means of maize DNA probes. Proc Natl Acad Sci USA 87: 4251–4255

    CAS  PubMed  Google Scholar 

  • Jones ES, Mahoney NL, Hayward MD, Armstead HI, Jones JG, Humphreys MO, King IP, Kishida T, Yamada T, Balfourier F, Charmet G, Forster JW (2002) An enhanced molecular marker based genetic map of perennial ryegrass (Lolium perenne) reveals comparative relationships with other Poaceae genomes. Genome 45:282–295

    Article  CAS  PubMed  Google Scholar 

  • Kosambi DD (1944) The estimation of map distances from recombination values. Ann Eugen 12:172–175

    Google Scholar 

  • Kurata N, Moore G, Nagamura Y, Foote T, Yano M, Minobe Y, Mike G (1994) Conservation of genome structure between rice and wheat. Biotechnology 12:276–278

    CAS  Google Scholar 

  • La Rota M, Sorrells ME (2004) Comparative DNA sequence analysis of mapped wheat ESTs reveals the complexity of genome relationships between rice and wheat. Funct Integr Genomics 4:34–46

    Google Scholar 

  • Lander ES, Green P, Abrahamson J, Barlow A, Daly MJ (1987) mapmaker: an interactive computer package for constructing primary genetic maps of experimental and natural populations. Genomics 1:174–181

    CAS  PubMed  Google Scholar 

  • Marino CL, Nelson JC, Lu YH, Sorrells ME, Leroy P, Tuleen NA, Lopes CR, Hart GE (1996) Molecular genetic maps of the group 6 chromosomes of hexaploid wheat (Triticum aestivum L. em. Thell). Genome 39:359–366

    CAS  Google Scholar 

  • Namuth DM, Lapitan NLV, Gill KS, Gill BS (1994) Comparative RFLP mapping of Hordeum vulgare and Triticum tauschii. Theor Appl Genet 89:865–872

    Google Scholar 

  • Nelson JC, Van Deynze AE, Autrique E, Sorrells ME, Lu YH, Merlino M, Atkinson M, Leroy P (1995a) Molecular mapping of wheat Homoeologous group 2. Genome 38:516–524

    CAS  Google Scholar 

  • Nelson JC, Van Deynze AE, Autrique E, Sorrells ME, Lu YH, Negre S, Bernard M, Leroy P (1995b) Molecular mapping of wheat Homoeologous group 3. Genome 38:525–533

    CAS  Google Scholar 

  • Ooijen JW van, Sandbrink JM, Vrielink M, Verkerk R, Zabel P, Lindhout P (1994) An RFLP linkage map of Lycopersicon peruvianum. Theor Appl Genet 89:1007–1013

    Google Scholar 

  • Saghai-Maroof MA, Soliman KM, Jorgensen RA, Allard RW (1984) Ribosomal DNA spacer-length polymorphisms in barley: Mendelian inheritance, chromosomal location, and population dynamics. Proc Natl Acad Sci USA 81:8014–8018

    PubMed  Google Scholar 

  • Soreng RJ, Davis JJ (1998) Phylogenetics and character evolution in the grass family (Poaceae): simultaneous analysis of morphological and chloroplast DNA restriction site character sets. Bot Rev 64:1–85

    Google Scholar 

  • Tanksley SD, Ganal MW, Prince JP, De Vincente MC, Bonierbale MW, Broun P, Fulton TM, Giovannoni JJ, Grandillo S, Martin GB, Messeguer R, Miller L, Paterson AH, Pineda O, RMS, Wing RA, Wu W, Young ND (1992) High-density molecular linkage maps of the tomato and potato genomes. Genetics 132:1141–1160

    CAS  PubMed  Google Scholar 

  • Thorogood D, Kaiser WJ, Jones JG, Armstead I (2002) Self-incompatibility in ryegrass 12. Genotyping and mapping the S and Z loci in Lolium perenne L. Heredity 88:385–390

    Article  CAS  PubMed  Google Scholar 

  • Van Deynze AE, Dubcovsky J, Gill KS, Nelson JC, Sorrells ME, Dvorak J, Gill BS, Lagudah ES, McCouch SR, Appels R (1995a) Molecular genetic maps for group 1 chromosomes of Triticeae species and their relation to chromosomes in rice and oat. Genome 38:45–59

    CAS  Google Scholar 

  • Van Deynze AE, Nelson JC, O’Donoghue LS, Ahan S, Siripoonwiwat W, Harrington SE, Yglesias ES, Braga DP, McCouch SR, Sorrells ME (1995b) Comparative mapping in grasses. Oat relationships. Mol Gen Genet 249:349–356

    CAS  Google Scholar 

  • Van Deynze AE, Nelson JC, Yglesias ES, Harrington SE, Braga DP, McCouch SR, Sorrells ME (1995c) Comparative mapping in grasses. Wheat relationships. Mol Gen Genet 248:744–754

    CAS  PubMed  Google Scholar 

  • Van Deynze AE, Sorrells ME, Park WD, Ayres NM, Fu H, Cartinhour SW, Paul E, McCouch SR (1998) Anchor probes for comparative mapping of grass genera. Theor Appl Genet 97:356–369

    Article  Google Scholar 

  • Warnke SE, Barker RE, Jung G, Sim SC, Rouf Mian MA, Saha MC, Brilman LA, Dupal MP, Forster JW (2004) Genetic linkage mapping of an annual×perennial ryegrass population. Theor Appl Genet 109:294–304

    Article  CAS  PubMed  Google Scholar 

  • Whitkus R, Doebley J, Lee M (1992) Comparative genome mapping of sorghum and maize. Genetics 132:1119–1130

    Google Scholar 

Download references

Acknowledgements

We thank Dr. S. McCouch of Cornell University, Ithaca, N.Y. and the USDA probes depository, Albany, Calif. for kindly providing the heterologous RFLP probes. We also thank Dr. Shawn Kaeppler, Dr. Rebecca Abler, and Dr. Zahi Atallah for their valuable comments and critical review and Lori Evans for handling plant materials. The Wisconsin Sod Producers Association and the Wisconsin Turfgrass Association provided partial funding.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to G. Jung.

Additional information

Communicated by J.S. Heslop-Harrison

Rights and permissions

Reprints and permissions

About this article

Cite this article

Sim, S., Chang, T., Curley, J. et al. Chromosomal rearrangements differentiating the ryegrass genome from the Triticeae, oat, and rice genomes using common heterologous RFLP probes. Theor Appl Genet 110, 1011–1019 (2005). https://doi.org/10.1007/s00122-004-1916-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00122-004-1916-1

Keywords

Navigation