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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical and applied genetics 68 (1984), S. 547-554 
    ISSN: 1432-2242
    Keywords: Wheat X rye hybrids ; Translocations ; Introgression ; Tissue culture ; C-banding
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The spontaneous occurrence of chromosome breaks, deletions, and translocations in plant tissue cultures is well documented. This study investigated the usefulness of tissue culture as a method of introgressing alien genes into wheat. Wheat X rye hybrids were regenerated from embryo scutellar calli maintained in culture for 222 days. The regenerated seedlings then were treated with colchicine to produce amphidiploids (AABBDDRR). The karyotypes of ten amphidiploids were analyzed by C-banding to determine chromosome structural changes that occurred during tissue culture. Three wheat/rye and one wheat/wheat chromosome translocations, seven deletions, and five amplifications of heterochromatin bands of rye chromosomes were identified. One amphidiploid contained a reciprocal translocation between wheat chromosome 4D and rye chromosome 1R. Non-reciprocal translocations between 2B and 3R, and between an unidentified wheat chromosome and 2R, were found independently in two amphidiploids. An additional plant had a translocation between wheat chromosomes 6B and 5A. All deletions involving rye chromosomes were noted in all 10 amphidiploids. Twelve of the 13 breakpoints in chromosomes involved in translocations and deletions occurred in heterochromatin. Amplification of heterochromatin bands on 2RL and 7RL chromosome arms also was observed in five plants. These results indicate a high degree of chromosome structural change induced by tissue culture. Therefore, tissue culture may be a useful tool in alien gene introgression and manipulation of heterochromatin in triticale improvement.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical and applied genetics 78 (1989), S. 625-632 
    ISSN: 1432-2242
    Keywords: Triticum aestivum ; Tissue culture ; Callus ; Monosomic analysis ; Regeneration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The ability of immature embryos of wheat (Triticum aestivum L.) to respond in cell culture was examined in crosses between the ‘Wichita’ monosomic series and a highly regenerable line, ‘ND7532’. Segregation in disomic controls and 13 monosomic families showed a good fit to a monogenic ratio indicating a qualitative mode of inheritance. Segregation in the cross involving monosomic 2D showed a high frequency of regeneration (93.6%) and high callus growth rate (1.87 g/90 days) indicating that 2D is a critical chromosome. Modifying genes may be located on other chromosomes. Substitution of chromosomes from a low regenerable cultivar ‘Vona’ further indicated that the group 2 chromosomes, in particular chromosome 2D, possess genetic factors promoting callus growth and regeneration.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical and applied genetics 78 (1989), S. 783-787 
    ISSN: 1432-2242
    Keywords: Tissue culture ; Callus ; Wheat ; Ditelosomics ; Nullisomic-tetrasomics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The ability of immature embryos of wheat (Triticum aestivum L.) to respond to tissue culture has been shown to involve the group 2 chromosomes. The available group 2 ditelosomic and nullisomic-tetrasomic lines of ‘Chinese Spring’ wheat were used to determine the chromosome arm location and chromosome dosage effect associated with the expression of tissue culture response (TCR). Significant differences were found between the aneuploid lines and the euploid control for the expression of both regenerable callus formation and callus growth rate. A model is proposed suggesting that a major TCR gene is located on 2DL and that 2AL and 2BS possess minor TCR genes. Furthermore, a major regulatory gene controlling the expression of TCR genes may be located on chromosome 2BL.
    Type of Medium: Electronic Resource
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