首页> 美国卫生研究院文献>BMC Genomics >Identification of Pou5f1 Sox2 and Nanog downstream target genes with statistical confidence by applying a novel algorithm to time course microarray and genome-wide chromatin immunoprecipitation data
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Identification of Pou5f1 Sox2 and Nanog downstream target genes with statistical confidence by applying a novel algorithm to time course microarray and genome-wide chromatin immunoprecipitation data

机译:通过将新算法应用于时程微阵列和全基因组染色质免疫沉淀数据以统计可信度鉴定Pou5f1Sox2和Nanog下游靶基因

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摘要

BackgroundTarget genes of a transcription factor (TF) Pou5f1 (Oct3/4 or Oct4), which is essential for pluripotency maintenance and self-renewal of embryonic stem (ES) cells, have previously been identified based on their response to Pou5f1 manipulation and occurrence of Chromatin-immunoprecipitation (ChIP)-binding sites in promoters. However, many responding genes with binding sites may not be direct targets because response may be mediated by other genes and ChIP-binding site may not be functional in terms of transcription regulation.
机译:背景转录因子(TF)Pou5f1(Oct3 / 4或Oct4)的靶基因对于胚胎干细胞(ES)的多能性维持和自我更新至关重要,先前已经根据它们对Pou5f1操纵的反应和是否存在这种基因而确定了它们的靶基因。启动子中的染色质免疫沉淀(ChIP)结合位点。但是,许多具有结合位点的响应基因可能不是直接的靶标,因为响应可能是由其他基因介导的,ChIP结合位点在转录调控方面可能不起作用。

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