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首页> 外文期刊>Theoretical and Applied Genetics >Construction of BAC and BIBAC libraries from sunflower and identification of linkage group-specific clones by overgo hybridization
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Construction of BAC and BIBAC libraries from sunflower and identification of linkage group-specific clones by overgo hybridization

机译:从向日葵构建BAC和BIBAC文库,并通过过度杂交鉴定连锁基团特异性克隆

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摘要

Complementary BAC and BIBAC libraries were constructed from nuclear DNA of sunflower cultivar HA 89. The BAC library, constructed with BamHI in the pECBAC1 vector, contains 107,136 clones and has an average insert size of 140 kb. The BIBAC library was constructed with HindIII in the plant-transformation-competent binary vector pCLD04541 and contains 84,864 clones, with an average insert size of 137 kb. The two libraries combined contain 192,000 clones and are equivalent to approximately 8.9 haploid genomes of sunflower (3,000 Mb/1C), and provide a greater than 99% probability of obtaining a clone of interest. The frequencies of BAC and BIBAC clones carrying chloroplast or mitochondrial DNA sequences were estimated to be 2.35 and 0.04%, respectively, and insert-empty clones were less than 0.5%. To facilitate chromosome engineering and anchor the sunflower genetic map to its chromosomes, one to three single- or low-copy RFLP markers from each linkage group of sunflower were used to design pairs of overlapping oligonucleotides (overgos). Thirty-six overgos were designed and pooled as probes to screen a subset (5.1×) of the BAC and BIBAC libraries. Of the 36 overgos, 33 (92%) gave at least one positive clone and 3 (8%) failed to hit any clone. As a result, 195 BAC and BIBAC clones representing 19 linkage groups were identified, including 76 BAC clones and 119 BIBAC clones, further verifying the genome coverage and utility of the libraries. These BAC and BIBAC libraries and linkage group-specific clones provide resources essential for comprehensive research of the sunflower genome.
机译:互补的BAC和BIBAC文库是由向日葵品种HA 89的核DNA构建的。BAC文库由pECBAC1载体中的BamHI构建,包含107,136个克隆,平均插入大小为140 kb。 BIBAC文库是在植物转化型二元载体pCLD04541中用HindIII构建的,包含84,864个克隆,平均插入片段大小为137 kb。合并的两个文库包含192,000个克隆,相当于向日葵的约8.9个单倍体基因组(3,000 Mb / 1C),并提供了超过99%的概率获得目标克隆。携带叶绿体或线粒体DNA序列的BAC和BIBAC克隆的频率分别估计为2.35和0.04%,而空插入克隆的频率小于0.5%。为了促进染色体工程并将向日葵遗传图谱锚定在其染色体上,使用向日葵每个连锁组中的一到三个单拷贝或低拷贝RFLP标记来设计重叠的寡核苷酸对。设计了36个片段,并汇总为探针,以筛选BAC和BIBAC文库的一部分(5.1x)。在这36例中,有33例(92%)给出了至少一个阳性克隆,而3例(8%)未能击中任何克隆。结果,鉴定出代表19个连接基团的195个BAC和BIBAC克隆,包括76个BAC克隆和119个BIBAC克隆,进一步验证了基因组的覆盖范围和实用性。这些BAC和BIBAC库以及特定于连接基团的克隆为全面研究向日葵基因组提供了必不可少的资源。

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  • 来源
    《Theoretical and Applied Genetics》 |2006年第1期|23-32|共10页
  • 作者单位

    Department of Plant Sciences North Dakota State University;

    US Department of Agriculture Agricultural Research Service Northern Crop Science Laboratory;

    Department of Soil and Crop Sciences and Institute for Plant Genomics and Biotechnology Texas AM University;

    Department of Soil and Crop Sciences and Institute for Plant Genomics and Biotechnology Texas AM University;

    US Department of Agriculture Agricultural Research Service Northern Crop Science Laboratory;

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