Skip to main content
Log in

C-banded karyotype of Thinopyrum bessarabicum and identification of its chromosomes in wheat background

  • Short Communication
  • Published:
Genetic Resources and Crop Evolution Aims and scope Submit manuscript

Abstract

C-banded pattern in two accessions of Thinopyrum bessarabicum (Save ex Rayss) A. Löve (2n = 2x = 14, EbEb) and their idiogram was established. C-banding analysis was further used to identify the chromosomes of Tritipyrum amphiploid (2n = 6x = 42, AABBEbEb) and a BC1F2 genotype from wheat and Tritipyrum. Two 18S-26S rDNA loci were detected on Th. bessarabicum chromosomes by in situ hybridization using an 18S-26S rDNA probe. Eb chromosomes in Tritipyrum generally were identified by their distinctive C-banding patterns which reflected heterochromatin regions. C-banding procedure resulted in sharp and distinct bands in one or both ends of Eb chromosomes without interval bands. Observed C-bands in Eb genome mainly reflected the telomeric and subtelomeric sequences which also showed more strong signals in genomic in situ hybridization. Results showed the importance of the C-banding technique as a screening tool in identification of addition and substitution lines in the progenies of wheat and Tritipyrum crosses during segregating generations.

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

References

  • Alonso LC, Kimber G (1980) A hybrid between Agropyron junceum and Triticum aestivum. Cereal Res Commun 8:355–358

    Google Scholar 

  • Chen PD, Gill BS (1983) The origin of chromosome 4A, and genomes B and G of tetraploid wheat. In: Sakamoto S (ed) Proceedings International wheat Genet Symposium 6th. pp 39–48

  • Dewey DR (1984) The genomic system of classification as a guide to intergeneric hybridization with the perennial Triticeae. In: Gustafson JP (ed) Gene manipulation in plant improvement. Plenum Press, New York, pp 209–279

    Google Scholar 

  • Dvorak J, Ross K (1986) Expression of tolerance of Na+, K+, Mg2+, Cl and SO4 2+ ions and sea water in the amphiploid of Triticum aestivum × Elytrigia elongata. Crop Sci 26:658–660

    Article  CAS  Google Scholar 

  • Endo TR, Gill BS (1984) The heterochromatic distribution and genome evolution in diploid species of Elymus and Agropyron. Can J Genet Cytol 26:669–678

    Google Scholar 

  • Francki MG, Langridge P (1994) The molecular identification of the midget chromosome from the rye genome. Genome 37:1056–1061

    Article  CAS  PubMed  Google Scholar 

  • Friebe B, Kim NS, Kuspira J, Gill BS (1990) Genetic and cytogenetic analysis of the A genome of Triticum monococcum. VI. Production and identification of primary trisomics using the C-banding technique. Genome 33:542–555

    CAS  Google Scholar 

  • Friebe B, Mukai Y, Gill BS (1992a) C-banding polymorphisms in several accessions of Triticum tauschii (Aegilops squarrosa). Genome 35:192–199

    Google Scholar 

  • Friebe B, Schubert V, Blüthner WD, Hammer K (1992b) C-banding pattern and polymorphism of Aegilops caudata and chromosomal constitutions of the amphiploid T. aestivumAe. caudata and six derived chromosome addition lines. Theor Appl Genet 83:589–596

    Google Scholar 

  • Friebe B, Tuleen N, Jiang J, Gill BS (1993) Standard karyotype of Triticum longissimum and its cytogenetic relationship with T. aestivum. Genome 36:731–742

    Article  CAS  PubMed  Google Scholar 

  • Gerlach WL, Bedbrook JR (1979) Cloning and characterization of ribosomal RNA genes from wheat and barley. Nucleic Acids Res 7:1869–1885

    Article  CAS  PubMed  Google Scholar 

  • Gill BS, Friebe B, Endo TR (1991) Standard karyotype and nomenclature system for description of chromosome bands and structural aberrations in wheat (Triticum aestivum). Genome 34:830–839

    Google Scholar 

  • Gorham J, McDonnell E, Budrewicz E, Wyn Jones RG (1985) Salt tolerance in the Triticeae: growth and solute accumulation in leaves of Thinopyrum bessarabicum. J Exp Bot 36:1021–1031

    Article  CAS  Google Scholar 

  • Jauhar PP (1992) Synthesis and cytological characterization of trigenerie hybrids involving durum wheat, Thinopyrum bessarabicum and Lophopyrum elongatum. Theor Appl Genet 84:511–519

    Google Scholar 

  • King IP, Law CN, Cant KA, Orford SE, Reader SM, Miller TE (1997) Tritipyrum, a potential new salt-tolerant cereal. Plant Breed 116:127–132

    Article  Google Scholar 

  • Levan A, Fredga K, Sandbreg A (1964) Nomenclature for centromeric position on chromosome. Hereditas 52:201–220

    Article  Google Scholar 

  • Mukai Y, Friebe B, Gill BS (1992) Comparison of C-banding patterns and in situ hybridization sites using highly repetitive and total genomic rye DNA probes of ‘Imperial’ rye chromosomes added to wheat. Jpn J Genet 67:71–83

    Article  Google Scholar 

  • Sepsi A, Molnár I, Szalay D, Molnár-Láng M (2008) Characterization of a leaf rust-resistant wheat–Thinopyrum ponticum partial amphiploid BE-1, using sequential multicolor GISH and FISH. Theor Appl Genet 116:825–834

    Article  CAS  PubMed  Google Scholar 

  • Shen X, Ohm H (2007) Molecular mapping of Thinopyrum-derived Fusarium head blight resistance in common wheat. Mol Breed 20:131–140

    Article  CAS  Google Scholar 

  • Stebbins GL (1971) Chromosome evolution in higher plants. Edward Arnold, London

    Google Scholar 

  • Wang RRC (2006) Registration of TBTE001 and TBTE002 Thinopyrum amphidiploid genetic stocks differing for leaf glaucousness. Crop Sci 46:1013–1014

    Article  Google Scholar 

  • William HM, Mujeeb-Kazi A (1993) Thinopyrum bessarabicum: biochemical and cytological markers for the detection of genetic introgression in its hybrid derivatives with Triticum aestivum L. Theor Appl Genet 86:365–370

    Article  Google Scholar 

Download references

Acknowledgments

The authors thank Professor Bikram S. Gill and Professor Bernd Friebe from Kansas State University, USA for providing the pTA71 clone and Dr. Goerge Fedak from AgriFood, Ottawa, Canada for providing Th. bessarabicum seeds. The first author gratefully acknowledges Dr. Michael Francki from Murdoch University, Australia for his advices on in situ hybridization.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to G. Mirzaghaderi.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Mirzaghaderi, G., Shahsevand Hassani, H. & Karimzadeh, G. C-banded karyotype of Thinopyrum bessarabicum and identification of its chromosomes in wheat background. Genet Resour Crop Evol 57, 319–324 (2010). https://doi.org/10.1007/s10722-009-9509-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10722-009-9509-0

Keywords

Navigation