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Genome-wide mapping of promoter-anchored interactions with close to single-enhancer resolution

机译:全基因组的启动子锚定相互作用的图谱,具有接近单个增强子的分辨率

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摘要

Although the locations of promoters and enhancers have been identified in several cell types, we still have limited information on their connectivity. We developed HiCap, which combines a 4-cutter restriction enzyme Hi-C with sequence capture of promoter regions. Applying the method to mouse embryonic stem cells, we identified promoter-anchored interactions involving 15,905 promoters and 71,984 distal regions. The distal regions were enriched for enhancer marks and transcription, and had a mean fragment size of only 699 bp - close to single-enhancer resolution. High-resolution maps of promoter-anchored interactions with HiCap will be important for detailed characterizations of chromatin interaction landscapes.
机译:尽管启动子和增强子的位置已在几种细胞类型中确定,但我们对它们的连通性仍然了解有限。我们开发了HiCap,它结合了4-切割限制酶Hi-C与启动子区域的序列捕获。将该方法应用于小鼠胚胎干细胞,我们确定了涉及15905个启动子和71984个远端区域的启动子锚定相互作用。远端区域富集了增强子标记和转录,并且平均片段大小仅为699 bp,接近单个增强子的分辨率。与HiCap的启动子锚定相互作用的高分辨率图对于染色质相互作用图谱的详细表征非常重要。

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