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Cancer-Associated noncoding mutations affect RNA G-quadruplex-mediated regulation of gene expression

机译:癌症相关的非编码突变影响RNA G-四链体介导的基因表达调控

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摘要

© 2017 The Author(s). Cancer is a multifactorial disease driven by a combination of genetic and environmental factors. Many cancer driver mutations have been characterised in protein-coding regions of the genome. However, mutations in noncoding regions associated with cancer have been less investigated. G-quadruplex (G4) nucleic acids are four-stranded secondary structures formed in guanine-rich sequences and prevalent in the regulatory regions. In this study, we used published whole cancer genome sequence data to find mutations in cancer patients that overlap potential RNA G4-forming sequences in 5′ UTRs. Using RNAfold, we assessed the effect of these mutations on the thermodynamic stability of predicted RNA G4s in the context of full-length 5′ UTRs. Of the 217 identified mutations, we found that 33 are predicted to destabilise and 21 predicted to stabilise potential RNA G4s. We experimentally validated the effect of destabilising mutations in the 5′ UTRs of BCL2 and CXCL14 and one stabilising mutation in the 5′ UTR of TAOK2. These mutations resulted in an increase or a decrease in translation of these mRNAs, respectively. These findings suggest that mutations that modulate the G4 stability in the noncoding regions could act as cancer driver mutations, which present an opportunity for early cancer diagnosis using individual sequencing information.
机译:©2017作者。癌症是由遗传和环境因素共同驱动的多因素疾病。在基因组的蛋白质编码区中已鉴定出许多癌症驱动突变。但是,与癌症相关的非编码区的突变研究较少。 G-四链体(G4)核酸是形成于富含鸟嘌呤的序列中的四链二级结构,并普遍存在于调节区中。在这项研究中,我们使用已发布的完整癌症基因组序列数据来发现癌症患者中与5'UTR中潜在的RNA G4形成序列重叠的突变。使用RNAfold,我们评估了这些突变对全长5'UTRs预测的RNA G4s热力学稳定性的影响。在217个已识别的突变中,我们发现有33个预计会不稳定,而21个预计会稳定潜在的RNA G4。我们通过实验验证了BCL2和CXCL14的5'UTR中不稳定突变和TAOK2的5'UTR中一个稳定突变的影响。这些突变分别导致这些mRNA的翻译增加或减少。这些发现表明,调节非编码区G4稳定性的突变可以充当癌症驱动突变,这为使用个体测序信息进行早期癌症诊断提供了机会。

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