Le Mai Nhu Uyen, Ning Yichong, Zhou Jianlin
State Key Laboratory of Developmental Biology of Freshwater Fish & Key Laboratory of Protein Chemistry and Developmental Biology of the Ministry of Education, College of Life Science, Hunan Normal University, Changsha, Hunan 410081, China.
Chongzuo Key Laboratory of Biomedical Clinical Transformation, The People's Hospital of Chongzuo, Youjiang Medical University for Nationalities, Chongzuo, Guangxi, China.
Data Brief. 2023 Aug 18;50:109499. doi: 10.1016/j.dib.2023.109499. eCollection 2023 Oct.
The tumor suppressor p53 exerts its role mainly as a transcription factor. The TP53 gene, which encodes the p53 protein, is the most commonly mutated gene in human cancers, particularly triple negative breast cancer (TNBC). Variations in the TP53 gene occur mainly in exons 5-8 and result in missense mutations in the DNA-binding domain of the p53 protein that alter DNA binding specificity. To identify the target genes of mutant p53, we performed chromatin immunoprecipitation followed by DNA microarray (ChIP-chip). Briefly, the TNBC cell line MDA-MB-468 containing the endogenous p53-R273H mutation (the arginine residue at position 273 is mutated to a histidine) was cross-linked with 1% formaldehyde and ultrasonically sheared to generate chromatin fragments in a range of 200∼1000 bp. An aliquot of the sheared chromatin was kept as input, and the other chromatin was precipitated with a p53 monoclonal antibody. DNA was purified from the precipitated chromatin and the unprecipitated chromatin (i.e., input), amplified, and labeled with Cy5 (ChIP DNA) or Cy3 (input DNA). Cy5- and Cy3-labeled DNA samples were cohybridized with the NimbleGen Human ChIP-chip 2.1 M Deluxe Promoter Array. The raw and analyzed data are described in this article. They are useful for identifying target genes and consensus binding motifs of the p53 R273H mutant and for further clarifying the molecular mechanism underlying the oncogenic activity of the p53 mutant.
肿瘤抑制因子p53主要作为一种转录因子发挥作用。编码p53蛋白的TP53基因是人类癌症中最常发生突变的基因,尤其是在三阴性乳腺癌(TNBC)中。TP53基因的变异主要发生在外显子5 - 8,导致p53蛋白DNA结合域中的错义突变,从而改变DNA结合特异性。为了鉴定突变型p53的靶基因,我们进行了染色质免疫沉淀结合DNA微阵列分析(ChIP-chip)。简要地说,含有内源性p53-R273H突变(第273位的精氨酸残基突变为组氨酸)的TNBC细胞系MDA-MB-468用1%甲醛交联,然后超声剪切以产生200∼1000 bp范围内的染色质片段。剪切后的染色质的一部分作为输入对照保留,另一部分染色质用p53单克隆抗体沉淀。从沉淀的染色质和未沉淀的染色质(即输入对照)中纯化DNA,进行扩增,并用Cy5(ChIP DNA)或Cy3(输入DNA)标记。Cy5和Cy3标记的DNA样品与NimbleGen人类ChIP-chip 2.1 M Deluxe启动子阵列共杂交。本文描述了原始数据和分析数据。它们有助于鉴定p53 R273H突变体的靶基因和共有结合基序,并进一步阐明p53突变体致癌活性的分子机制。