Kainov Yaroslav, Hamid Fursham, Makeyev Eugene V
Centre for Developmental Neurobiology, King's College London, London, United Kingdom.
Department of Medical and Molecular Genetics, King's College London, London, United Kingdom.
Elife. 2024 Dec 11;13:RP99040. doi: 10.7554/eLife.99040.
The expression of eukaryotic genes relies on the precise 3'-terminal cleavage and polyadenylation of newly synthesized pre-mRNA transcripts. Defects in these processes have been associated with various diseases, including cancer. While cancer-focused sequencing studies have identified numerous driver mutations in protein-coding sequences, noncoding drivers - particularly those affecting the cis-elements required for pre-mRNA cleavage and polyadenylation - have received less attention. Here, we systematically analysed somatic mutations affecting 3'UTR polyadenylation signals in human cancers using the Pan-Cancer Analysis of Whole Genomes (PCAWG) dataset. We found a striking enrichment of cancer-specific somatic mutations that disrupt strong and evolutionarily conserved cleavage and polyadenylation signals within tumour suppressor genes. Further bioinformatics and experimental analyses conducted as a part of our study suggest that these mutations have a profound capacity to downregulate the expression of tumour suppressor genes. Thus, this work uncovers a novel class of noncoding somatic mutations with significant potential to drive cancer progression.
真核基因的表达依赖于新合成的前体信使核糖核酸(pre-mRNA)转录本精确的3'末端切割和多聚腺苷酸化。这些过程中的缺陷与包括癌症在内的各种疾病有关。虽然聚焦于癌症的测序研究已经在蛋白质编码序列中鉴定出许多驱动突变,但非编码驱动因素——特别是那些影响前体mRNA切割和多聚腺苷酸化所需顺式元件的驱动因素——受到的关注较少。在这里,我们使用全基因组泛癌分析(PCAWG)数据集系统地分析了影响人类癌症中3'非翻译区(3'UTR)多聚腺苷酸化信号的体细胞突变。我们发现,在肿瘤抑制基因中,破坏强的且在进化上保守的切割和多聚腺苷酸化信号的癌症特异性体细胞突变显著富集。作为我们研究的一部分进行的进一步生物信息学和实验分析表明,这些突变具有下调肿瘤抑制基因表达的强大能力。因此,这项工作揭示了一类新的非编码体细胞突变,它们具有驱动癌症进展的巨大潜力。