Kouprina Natalay, Larionov Vladimir
Laboratory of Molecular Pharmacology, National Cancer Institute, National Institutes of Health, 9000 Rockville Pike, Bethesda, Maryland 20892, USA.
Nat Protoc. 2008;3(3):371-7. doi: 10.1038/nprot.2008.5.
Here, we describe a protocol for the selective isolation of any genomic fragment or gene of interest up to 250 kb in size from complex genomes as a circular yeast artificial chromosome (YAC). The method is based on transformation-associated recombination (TAR) in the yeast Saccharomyces cerevisiae between genomic DNA and a linearized TAR cloning vector containing targeting sequences homologous to a region of interest. Recombination between the vector and homologous sequences in the co-transformed mammalian DNA results in the establishment of a YAC that is able to propagate, segregate and be selected for in yeast. Yield of gene-positive clones varies from 1% to 5%. The entire procedure takes 2 weeks to complete once the TAR vector is constructed and genomic DNA is prepared. The TAR cloning method has a broad application in functional and comparative genomics, long-range haplotyping and characterization of chromosomal rearrangements, including copy number variations.
在此,我们描述了一种从复杂基因组中选择性分离大小达250 kb的任何感兴趣的基因组片段或基因的方法,该方法可将其作为环状酵母人工染色体(YAC)进行分离。该方法基于酿酒酵母中的转化相关重组(TAR),即在基因组DNA与含有与感兴趣区域同源的靶向序列的线性化TAR克隆载体之间进行重组。载体与共转化的哺乳动物DNA中的同源序列之间的重组导致形成一个能够在酵母中繁殖、分离并被选择的YAC。基因阳性克隆的产量在1%至5%之间。一旦构建好TAR载体并制备好基因组DNA,整个过程需要2周时间才能完成。TAR克隆方法在功能和比较基因组学、长程单倍型分析以及染色体重排(包括拷贝数变异)的表征方面具有广泛应用。