首页> 外文期刊>Theoretical and Applied Genetics: International Journal of Breeding Research and Cell Genetics >Flow cytometric chromosome sorting from diploid progenitors of bread wheat, T. urartu, Ae. speltoides and Ae. tauschii.
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Flow cytometric chromosome sorting from diploid progenitors of bread wheat, T. urartu, Ae. speltoides and Ae. tauschii.

机译:从面包小麦二倍体祖细胞流式细胞仪染色体分选,T。urartu,Ae。 speltoides和Ae。陶希

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摘要

The three subgenomes of hexaploid bread wheat originated from Triticum urartu (AuAu), from a species similar to Aegilops speltoides (SS) (progenitor of the B genome), and from Ae. tauschii (DD). Earlier studies indicated the potential of chromosome genomics to assist gene transfer from wild relatives of wheat and discover novel genes for wheat improvement. This study evaluates the potential of flow cytometric chromosome sorting in the diploid progenitors of bread wheat. Flow karyotypes obtained by analysing DAPI-stained chromosomes were characterized and the contents of the chromosome peaks were determined. FISH analysis with repetitive DNA probes proved that chromosomes 5Au, 5S and 5D could be sorted with purities of 78-90%, while the remaining chromosomes could be sorted in groups of three. Twenty-five conserved orthologous set (COS) markers covering wheat homoeologous chromosome groups 1-7 were used for PCR with DNA amplified from flow-sorted chromosomes and genomic DNA. These assays validated the cytomolecular results as follows: peak I on flow karyotypes contained chromosome groups 1, 4 and 6, peak II represented homoeologous group 5, while peak III consisted of groups 2, 3 and 7. The isolation of individual chromosomes of wild progenitors provides an attractive opportunity to investigate the structure and evolution of the polyploid genome and to deliver tools for wheat improvement.
机译:六倍体面包小麦的三个亚基因组起源于urartu小麦(A u A u ),来自与Aegilops speltoides(SS)(B基因组的祖先)相似的物种,和爱陶西(DD)。较早的研究表明,染色体基因组学可能有助于从小麦野生近缘种转移基因并发现用于改良小麦的新基因。本研究评估了面包小麦二倍体祖细胞中流式细胞仪染色体分选的潜力。表征通过分析DAPI染色的染色体获得的流型核型,并确定染色体峰的含量。用重复DNA探针进行的FISH分析证明,5A u ,5S和5D染色体可以以78-90%的纯度进行分类,而其余染色体可以以三组的形式进行分类。使用覆盖小麦同源染色体组1-7的二十五个保守直系同源序列(COS)标记物进行PCR,并从分流后的染色体和基因组DNA中扩增出DNA。这些测定法验证了以下细胞分子结果:流动核型的峰I包含染色体组1、4和6,峰II代表同源组5,而峰III包括组2、3和7。野生祖细胞的单个染色体分离提供了一个诱人的机会来研究多倍体基因组的结构和进化,并提供了改良小麦的工具。

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