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Isolation of cDNA clones using yeast artificial chromosome probes

机译:使用酵母人工染色体探针分离cDNA克隆

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The cloning of large DNA fragments of hundreds of kilobases in Yeast artificial chromosomes, has simplified the analysis of regions of the genome previously cloned by cosmid walking. The mapping of expressed sequences within cosmid contigs has relied on the association of genes with sequence motifs defined by rare-cutting endonucleases, and the identification of sequence conservation between species. We reasoned that if the contribution of repetitive sequences to filter hybridisations could be minimised, then the use of large cloned DNAs as hybridisation probes to screen cDNA libraries would greatly simplify the characterisation of hitherto unidentified genes. In this paper we demonstrate the use of this approach by using a YAC, containing 180kb of human genomic DNA including the aldose reductase gene, as a probe to isolate an aldose reductase cDNA from a λgt11 human foetal liver cDNA library.
机译:酵母人工染色体中数百千个碱基的大DNA片段的克隆简化了先前通过粘粒行走而克隆的基因组区域的分析。粘粒重叠群中表达序列的作图依赖于基因与稀有核酸内切酶定义的序列基序的关联,以及物种间序列保守性的鉴定。我们认为,如果可以将重复序列对过滤杂交的贡献降到最低,那么使用大型克隆DNA作为杂交探针筛选cDNA文库将大大简化迄今为止尚未鉴定的基因的鉴定。在本文中,我们通过使用包含180kb人类基因组DNA(包括醛糖还原酶基因)的YAC作为探针从λgt11人胎肝cDNA文库中分离醛糖还原酶cDNA的方法,证明了该方法的使用。

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