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首页> 外文期刊>OMICS: A journal of integrative biology >ChIP-on-Chip Analysis of In Vivo Mutant p53 Binding To Selected Gene Promoters
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ChIP-on-Chip Analysis of In Vivo Mutant p53 Binding To Selected Gene Promoters

机译:ChIP-on-Chip体内突变型p53的分析绑定到选择基因启动子

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Growing evidence shows that mutant p53 proteins, which are present in many human tumors, gain oncogenic activities that can actively contribute to tumorigenesis. Mutant p53 proteins have been extensively shown to affect the expression of several genes involved in various aspects of cancer biology. We show here the ChIP-on-chip analysis of mutant p53 binding to a set of 154 promoters, composed of both validated and putative mutant p53 target genes. By using the chromatin obtained from mutant p53R175H-immunoprecipitation in proliferating SKBr3 breast cancer cells, we found that mutant p53 binds to 40 of the 154 promoters analyzed. siRNA-mediated mutant p53 knock-down modulates the transcript abundance of some of these target genes. Two-thirds of the mutant p53- bound promoters were also engaged by either p300 or PCAF acetyl-transferases, strongly indicating the presence of transcriptionally active complexes. We also found that NF-kB binding sites are overrepresented among the mutant p53-bound promoters; a ChIP-on-chip analysis confirmed that NF-kB p65 binds to 27 of the mutant p53-bound promoters, indicating that mutant p53 could influence the transcriptional output of these NF-kB target genes.
机译:越来越多的证据表明,突变型p53蛋白,在许多人类肿瘤的存在,获得吗致癌的活动可以积极地贡献肿瘤发生。广泛影响的表达多个基因参与的各个方面癌症生物学。分析突变型p53绑定一组154人启动子,验证和组成假定的突变型p53基因目标。染色质获得突变体p53R175H-immunoprecipitation在增殖SKBr3乳腺癌细胞,我们发现突变p53结合40 154启动子的分析。siRNA-mediated突变型p53可拆卸的调节记录大量的这些目标基因。发起人也通过p300或订婚了PCAF acetyl-transferases,强烈表示转录活性复合物的存在。我们还发现NF-kB结合位点在突变p53-bound过多促进剂;NF-kB p65结合突变p53-bound 27推动者,这表明p53突变这些影响转录输出NF-kB目标基因。

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