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通过酵母酿酒酵母中与转化相关的重组克隆从复杂基因组中选择性分离基因组位点。

Selective isolation of genomic loci from complex genomes by transformation-associated recombination cloning in the yeast Saccharomyces cerevisiae.

作者信息

Kouprina Natalay, Larionov Vladimir

机构信息

Laboratory of Molecular Pharmacology, National Cancer Institute, National Institutes of Health, 9000 Rockville Pike, Bethesda, Maryland 20892, USA.

出版信息

Nat Protoc. 2008;3(3):371-7. doi: 10.1038/nprot.2008.5.

Abstract

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.

摘要

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。

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