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Origin, dispersal and genomic structure of a low-copy-number hypervariable RFLP clone in Triticum and Aegilops species

机译:小麦和小麦的低拷贝数高变RFLP克隆的起源,扩散和基因组结构

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摘要

The genome of common wheat has evolved through allopolyploidization of three ancestral diploid genomes. A previously identified restriction fragment length polymorphism (RFLP) marker, pTag546, has the unique feature of showing hypervariability among closely related common wheat cultivars. To understand the origin and the mode of dispersal of this hypervariable sequence in the wheat genome, the distribution and structure of the homologous sequences were studied using ancestral diploid species, tetraploid disomic substitution lines and synthetic hexaploid lines. Comparative Southern blot and PCR analyses suggested that pTag546 homologs in the tetraploid and hexaploid wheat were derived from the S genome of Aegilops speltoides. Some pTag546 homologs were found to have transposed to A and D genomes in polyploid wheat. Evidence of transposition and elimination in some synthetic hexaploid lines was also obtained by comparing their copy numbers with those in the parental lines. Southern blot analysis of a genomic clone using a contiguous subset of sequences as probes revealed a core region of hypervariability that coincided with the region containing pTag546. No obvious structural characteristics that could explain the hypervariability, however, were found around the pTag546 sequence, except for accumulation of small repetitive sequences at one border. It was concluded that pTag546 increased its copy number through yet unknown mechanism(s) of transposition to various chromosomal locations over the period of allopolyploid evolution and during the artificial genome manipulation in wheat.
机译:普通小麦的基因组通过三个祖先二倍体基因组的同种多倍体化而进化。先前确定的限制性片段长度多态性(RFLP)标记pTag546具有独特的功能,可显示密切相关的普通小麦品种之间的高变异性。为了了解这种高变序列在小麦基因组中的起源和分布方式,使用祖先二倍体物种,四倍体二体代换系和合成六倍体系研究了同源序列的分布和结构。比较性Southern印迹和PCR分析表明,四倍体和六倍体小麦中的pTag546同源物来自Segatops speltoides的S基因组。在多倍体小麦中发现一些pTag546同源物已转座到A和D基因组。通过比较它们与亲本系的拷贝数也获得了一些合成六倍体系的转座和消除的证据。使用序列的连续子集作为探针的基因组克隆的Southern印迹分析揭示了高变异性核心区域,该区域与包含pTag546的区域重合。但是,除了在一个边界处积累了小的重复序列外,在pTag546序列周围没有发现可以解释高变异性的明显结构特征。结论是,pTag546通过异源多倍体进化期间以及在小麦的人工基因组操作过程中,通过未知机制的转座而增加了其拷贝数,所述转座至各种染色体位置。

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