Translational Oncogenomics Unit, Regina Elena Cancer Institute, Rome, Italy.
OMICS. 2011 May;15(5):305-12. doi: 10.1089/omi.2010.0084. Epub 2011 Feb 19.
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.
越来越多的证据表明,存在于许多人类肿瘤中的突变型 p53 蛋白获得了致癌活性,这些活性可积极促进肿瘤发生。突变型 p53 蛋白已被广泛证明可影响涉及癌症生物学各个方面的几个基因的表达。我们在此展示了突变型 p53 与一组 154 个启动子结合的 ChIP-on-chip 分析,这些启动子由已验证和推测的突变型 p53 靶基因组成。通过使用在增殖的 SKBr3 乳腺癌细胞中突变型 p53R175H 免疫沉淀获得的染色质,我们发现突变型 p53 结合到分析的 154 个启动子中的 40 个。siRNA 介导的突变型 p53 敲低调节了其中一些靶基因的转录丰度。三分之二的突变型 p53 结合启动子也被 p300 或 PCAF 乙酰转移酶结合,强烈表明存在转录活性复合物。我们还发现 NF-kB 结合位点在突变型 p53 结合启动子中过度表达;ChIP-on-chip 分析证实 NF-kB p65 结合到 27 个突变型 p53 结合启动子,表明突变型 p53 可能影响这些 NF-kB 靶基因的转录输出。