Wang Haoyi, Heinz Michael E, Crosby Seth D, Johnston Mark, Mitra Robi D
Department of Genetics, Washington University, School of Medicine, Genome Sequencing Center, St Louis, Missouri 63108, USA.
Nat Protoc. 2008;3(10):1569-77. doi: 10.1038/nprot.2008.148.
We present a protocol for a novel method for identifying the targets of DNA-binding proteins in the genome of the yeast Saccharomyces cerevisiae. This is accomplished by engineering a DNA-binding protein so that it leaves behind in the genome a permanent mark -- a 'calling card' -- that provides a record of that protein's visit to that region of the genome. The calling card is the yeast Ty5 retrotransposon, whose integrase interacts with the Sir4 protein. If Sir4 is fused to a DNA-binding protein, it recruits the Ty5 integrase, which directs insertion of a Ty5 calling card into the genome. The calling card along with the flanking genomic DNA is harvested by inverse PCR and its genomic location is determined by hybridization of the product to a DNA microarray. This method provides a straightforward alternative to the 'ChIP-chip' method for determining the targets of DNA-binding proteins. This protocol takes approximately 2 weeks to complete.
我们提出了一种用于鉴定酿酒酵母基因组中DNA结合蛋白靶标的新方法的方案。这是通过对一种DNA结合蛋白进行工程改造来实现的,使其在基因组中留下一个永久性标记——一张“名片”,该标记记录了该蛋白对基因组该区域的访问情况。这张名片就是酵母Ty5逆转座子,其整合酶与Sir4蛋白相互作用。如果将Sir4与一种DNA结合蛋白融合,它会招募Ty5整合酶,后者将Ty5名片插入基因组中。通过反向PCR收集名片及其侧翼基因组DNA,并通过将产物与DNA微阵列杂交来确定其基因组位置。这种方法为确定DNA结合蛋白的靶标提供了一种比“芯片免疫沉淀”方法更直接的替代方法。该方案大约需要2周时间完成。