Distorted segregation of RFLP markers in regenerated plants derived from another culture of an F1 hybrid of rice

  • Yamagishi Masumi
    Research Institute of Agricultural Resources, Ishikawa Agricultural College
  • Yano Masahiro
    Hokuriku National Agricultural Experimental Station, MAFF
  • Fukuta Yoshimichi
    Hokuriku National Agricultural Experimental Station, MAFF
  • Fukui Kiichi
    Hokuriku National Agricultural Experimental Station, MAFF
  • Otani Motoyasu
    Research Institute of Agricultural Resources, Ishikawa Agricultural College
  • Shimada Takiko
    Research Institute of Agricultural Resources, Ishikawa Agricultural College

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タイトル別名
  • Distorted segregation of RFLP markers in regenerated plants derived from anther culture of an Fl hybrid of rice.
  • Distorted segregation of RFLP markers i

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To examine whether parental alleles were randomly transmitted from heterozygous donor plants to anther culture (AC)-derived plants, two AC-derived populations and one F2 population in rice were compared for 50 RFLP markers distributed on the rice chromosomes. Two populations which were developed through different anther culture methods (the ordinary method and the direct regeneration method) and the F2 population were produced from an F1 hybrid between distantly related cultivars of Nipponbare (japonica type) and Milyang 23 (indica type). RFLP analysis revealed that ten and eleven of the 50 markers in the two AC-derived populations showed distorted segregation ratios from the theoretical ratio of 1:1. Parental alleles were not randomly transmitted from the F1 plant to the AC-derived plants. Additionally, the segregation ratios of seven and six RFLP markers, respectively, were distorted both from the 1:1 ratios and from the observed ratios in the F2 population. The chromosomal regions involving these markers were on chromosomes 1, 3, 7, 10, 11 and 12. Some of the regions were different in the two AC-derived populations. Non-random assortment of parental alleles might be influenced by anther culture methods.<br>

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