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构建用于克隆抗条锈病基因的六倍体小麦(普通小麦)细菌人工染色体文库。

Construction of a hexaploid wheat (Triticum aestivum L.) bacterial artificial chromosome library for cloning genes for stripe rust resistance.

作者信息

Ling P, Chen X M

机构信息

U.S. Department of Agriculture, Agricultural Research Service, Wheat Genetics, Quality, Physiology and Disease Research Unit, Pullman, WA 99164-6430, USA.

出版信息

Genome. 2005 Dec;48(6):1028-36. doi: 10.1139/g05-078.

Abstract

A hexaploid wheat (Triticum aestivum L.) bacterial artificial chromosome (BAC) library was constructed for cloning Yr5 and other genes conferring resistance to stripe rust (Puccinia striiformis f. sp. tritici). Intact nuclei from a Yr5 near-isogenic line were used to isolate high molecular weight DNA, which was partially cleaved with HindIII and cloned into pECBAC1 and pIndigoBAC-5 vectors. The wheat BAC library consisted of 422,400 clones arrayed in 1100 micro-titer plates (each plate with 384 wells). Random sampling of 300 BAC clones indicated an average insert size of 140 kb, with a size range from 25 to 365 kb. Ninety percent of the clones in the library had an insert size greater than 100 kb and fewer than 5% of the clones did not contain inserts. Based on an estimated genome size of 15,966 Mb for hexaploid wheat, the BAC library was estimated to have a total coverage of 3.58x wheat genome equivalents, giving approximately 96% probability of identifying a clone representing any given wheat DNA sequence. Twelve BAC clones containing an Yr5 locus-specific marker (Yr5STS7/8) were successfully selected by PCR screening of 3-dimensional BAC pools. The results demonstrated that the T. aestivum BAC library is a valuable genomic resource for positional cloning of Yr5. The library also should be useful in cloning other genes for stripe rust resistance and other traits of interest in hexaploid wheat.

摘要

构建了一个六倍体小麦(普通小麦)细菌人工染色体(BAC)文库,用于克隆Yr5及其他抗条锈病(条形柄锈菌小麦专化型)基因。利用Yr5近等基因系的完整细胞核分离高分子量DNA,用HindIII进行部分酶切,并克隆到pECBAC1和pIndigoBAC - 5载体中。该小麦BAC文库由422,400个克隆组成,排列在1100个微量滴定板中(每个板有384孔)。对300个BAC克隆进行随机抽样表明,平均插入片段大小为140 kb,大小范围为25至365 kb。文库中90%的克隆插入片段大小大于100 kb,不到5%的克隆不含插入片段。基于六倍体小麦估计的基因组大小为15,966 Mb,该BAC文库估计总覆盖度为3.58倍小麦基因组当量,识别代表任何给定小麦DNA序列的克隆的概率约为96%。通过对三维BAC池进行PCR筛选,成功选出了12个含有Yr5基因座特异性标记(Yr5STS7/8)的BAC克隆。结果表明,普通小麦BAC文库是用于Yr5图位克隆的宝贵基因组资源。该文库也应有助于克隆其他抗条锈病基因以及六倍体小麦其他感兴趣的性状基因。

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