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Wheat chromosome instability in the selfed progeny of the double monosomics 1Rv-1A

机译:小麦染色体在双重单体学的自私后代1RV-1A的稳定性

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摘要

Structural alterations of chromosomes are often found in wheat-rye hybrids. In the majority of cases modifications are observed for rye chromosomes, yet chromosome aberration cases are described for wheat, including the progeny of Triticum aestivum disomic and monosomic addition lines. Since wheat-rye substitution and translocation lines are the source of rye chromatin in wheat breeding programs, the information on possible chromosome changes in the genomes of introgressive forms is important. Chromosome behavior in F~(1)meiosis and chromosomal composition of F~(2)karyotypes for double monosomics 1Rv-1A were studied by applying C-banding, genomic in situ hybridisation (GISH) using rye genomic DNA, and sequential in situ hybridization using repetitive sequences pAs1, pSc119.2 and centromere specific pAet-06 as probes. The double monosomics 1Rv-1A were obtained by crossing of disomic substitution line with chromosome 1A replaced by Secale cereale 1Rv in the bread wheat Saratovskaya 29 (S29) background with S29. The results indicated a high frequency of bipolar chromosome 1Rv orientation, as compared to 1A, at metaphase I (MI) (58.6 and 34.7 % of meiocytes, respectively), and, at anaphase I (AI), chromatid segregation of 1Rv compared to 1A (70.53 and 32.14 % of meiocytes, respectively). In few cases desynapsis of wheat homologues was observed, at AI, the chromosomes randomly distributed between the poles or underwent chromatid segregation. At AI, the two wheat homologues separated onto sister chromatids in 10.89 % of cells.The plants F2 karyotypes were marked with aneuploidy not only of chromosomes 1A and 1Rv, but also of 1D, 2D, 3D, 3B, 3A, 4A, 6D, 6B, 6A, and 7D. Structural changes were observed for the chromosomes of the first homoeologous group (1Rv, 1A, 1D, 1B), as well as for 2B, 5D, 6B, and 7B. The chromosomes 1Rv and 6B often demonstrated aberrations. The types of aberrations were centromeric break, deletions of various sizes, and a changed repeat pSc119.2 localization pattern.
机译:染色体的结构改变通常在小麦 - 黑麦杂交物中发现。在大多数情况下,针对黑麦染色体观察到修饰,又用于小麦的染色体畸变病例,包括小麦的症状和​​单体添加线的后代。由于小麦 - 黑麦替代和易位线是小麦育种计划中黑麦染色质的来源,因此有关循环形式的可能性染色体变化的信息很重要。通过使用Rye基因组DNA施用C键,基因组,使用Rye基因组DNA来研究F〜(2)核苷酸和F〜(2)核型的染色体组合物的F〜(2)核型组成。使用重复序列PAS1,PSC119.2和CENTROMERE特异性PAET-06作为探针。通过用S29中的面包小麦Saratovskaya 29(S29)背景中的染色体1a替换为染色体1a,通过用染色体1a替代的染色体1a来获得双单体素1a。结果表明了双极染色体1RV取向的高频率,与1A相比,在中期I(MI)(分别为58.6和34.7%的Meiocytes),并且在Anaphase I(AI)中,与1A相比,1RV的染色体偏析。 (70.53和32.14%的Meiocytes)。在少数情况下,在AI,在杆子之间随机分布或接受染色体偏析,观察到小麦同源物的脱炔叶。在AI,两颗小麦同源物在10.89%的细胞中分离在姐妹染色体上。该植物F2核型不仅用染色体1a和1RV而标记,还具有1d,2d,3d,3b,3a,4a,6d,图6B,6A和7D。对于第一种同源基团(1RV,1A,1D,1B)以及2B,5D,6B和7B的染色体观察到结构变化。染色体1RV和6B通常展示像差。像差的类型是焦化的断裂,缺失各种尺寸,以及改变的重复PSC119.2定位模式。

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  • 来源
    《Journal of neurosurgical sciences》 |2018年第2期|共9页
  • 作者单位

    Institute of Cytology and Genetics of Siberian Branch of the Russian Academy of Sciences;

    Institute of Cytology and Genetics of Siberian Branch of the Russian Academy of Sciences;

    Institute of Cytology and Genetics of Siberian Branch of the Russian Academy of Sciences;

    Institute of Genetics and Cytology of National Academy of Sciences of Belarus;

    Institute of Genetics and Cytology of National Academy of Sciences of Belarus;

    Institute of Genetics and Cytology of National Academy of Sciences of Belarus;

    Institute of Genetics and Cytology of National Academy of Sciences of Belarus;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 头部及神经外科学;
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