Pouladi Nasser, Kouhsari Shideh Montasser, Feizi Mohammadali Hosseinpour, Gavgani Reyhaneh Ravanbakhsh, Azarfam Parvin
Department of Cellular and Molecular Biology, School of Biology, College of Sciences, University of Tehran, Tabriz, Iran.
Asian Pac J Cancer Prev. 2013;14(6):3503-7. doi: 10.7314/apjcp.2013.14.6.3503.
Although the majority of investigations concerned with TP53 and its protein have focused on coding regions, recently a set of studies highlighted significant roles of regulatory elements located in p53 mRNA, especially 5 ? UTR. The wrap53α transcript is one of those that acts as a natural antisense agent, forming RNA-RNA hybrids with p53 mRNA and protecting it from degradation.
In this study, we focused on the mutation status of exon 1α of the WRAP53 gene (according to exon 1 of p53) in 160 breast tumor tissue samples and conducted a bioinformatics search for probable miRNA binding site in the p53/wrap53 overlapping region. Mutations were detected, using single stranded conformation polymorphism (SSCP) and sequencing. We applied the miRBase database for prediction of miRNAs which target overlapping region of p53/wrap53 transcripts.
Our results showed all samples to have wild type alleles in exon 1 of TP53 gene. We could detect a novel and unreported intronic mutation (IVS1+ +56, G>C) outside overlapping regions of p53/wrap53 genes in breast cancer tissues and also predict the presence of a binding site for miR-4732-5p in the 5' UTR of Wrap53 mRNA.
From our findings we propose designing further studies focused on overexpression of miRNA-4732-5p and introducing different mutations in the overlapping region of wrap53 and p53 genes in order to study their effects on p53 and its δN isoform (δ40p53) expression. The results may provide new pieces in the p53 targeting puzzle for cancer therapy.
尽管大多数关于TP53及其蛋白的研究都集中在编码区,但最近一系列研究强调了位于p53 mRNA中的调控元件的重要作用,尤其是5′非翻译区(UTR)。Wrap53α转录本就是其中之一,它作为一种天然反义因子,与p53 mRNA形成RNA - RNA杂交体并保护其不被降解。
在本研究中,我们聚焦于160例乳腺肿瘤组织样本中WRAP53基因外显子1α(根据p53的外显子1)的突变状态,并对p53 / wrap53重叠区域中可能的miRNA结合位点进行了生物信息学搜索。使用单链构象多态性(SSCP)和测序检测突变。我们应用miRBase数据库预测靶向p53 / wrap53转录本重叠区域的miRNA。
我们的结果显示所有样本在TP53基因外显子1中均具有野生型等位基因。我们在乳腺癌组织中检测到p53 / wrap53基因重叠区域外的一个新的未报道的内含子突变(IVS1 + +56,G>C),并且还预测了Wrap53 mRNA的5′UTR中存在miR - 4732 - 5p的结合位点。
根据我们的研究结果,我们建议进一步开展研究,重点关注miRNA - 4732 - 5p的过表达,并在wrap53和p53基因的重叠区域引入不同突变,以研究它们对p53及其δN异构体(δ40p53)表达的影响。这些结果可能为癌症治疗的p53靶向难题提供新的线索。