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首页> 外文期刊>Current Genetics >A Blumeria graminis f.sp. hordei BAC library – contig building and microsynteny studies
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A Blumeria graminis f.sp. hordei BAC library – contig building and microsynteny studies

机译:Blumeria graminis f.sp. hordei BAC库–重叠群构建和微同调研究

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摘要

A bacterial artificial chromosome (BAC) library of Blumeria graminis f.sp. hordei, containing 12,000 clones with an average insert size of 41 kb, was constructed. The library represents about three genome equivalents and BAC-end sequencing showed a high content of repetitive sequences, making contig-building difficult. To identify overlapping clones, several strategies were used: colony hybridisation, PCR screening, fingerprinting techniques and the use of single-copy expressed sequence tags. The latter proved to be the most efficient method for identification of overlapping clones. Two contigs, at or close to avirulence loci, were constructed. Single nucleotide polymorphism (SNP) markers were developed from BAC-end sequences to link the contigs to the genetic maps. Two other BAC contigs were used to study microsynteny between B. graminis and two other ascomycetes, Neurospora crassa and Aspergillus fumigatus. The library provides an invaluable tool for the isolation of avirulence genes from B. graminis and for the study of gene synteny between this fungus and other fungi.
机译:布鲁氏杆菌f.sp.的细菌人工染色体(BAC)文库。构建了含有12,000个平均插入片段大小为41 kb的克隆的hordei。该文库代表约三个基因组当量,并且BAC末端测序显示出高含量的重复序列,从而难以构建重叠群。为了鉴定重叠克隆,使用了几种策略:菌落杂交,PCR筛选,指纹技术和单拷贝表达的序列标签的使用。后者被证明是鉴定重叠克隆的最有效方法。在无毒力基因座处或附近,构建了两个重叠群。从BAC末端序列开发了单核苷酸多态性(SNP)标记,以将重叠群与遗传图谱联系起来。其他两个BAC重叠群被用来研究B. graminis和另外两个子囊菌,克雷索氏菌和烟曲霉之间的微同调。该文库提供了一种宝贵的工具,可用于从革兰氏芽孢杆菌中分离无毒力基因,并用于研究这种真菌与其他真菌之间的基因同源性。

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