Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli Federico II, Naples 80136, Italy.
CEINGE Biotecnologie Avanzate, Naples 80145, Italy.
Hum Mol Genet. 2022 Mar 21;31(6):863-874. doi: 10.1093/hmg/ddab293.
The 10q24.33 locus is known to be associated with susceptibility to cutaneous malignant melanoma (CMM), but the mechanisms underlying this association have been not extensively investigated. We carried out an integrative genomic analysis of 10q24.33 using epigenomic annotations and in vitro reporter gene assays to identify regulatory variants. We found two putative functional single nucleotide polymorphisms (SNPs) in an enhancer and in the promoter of OBFC1, respectively, in neural crest and CMM cells, one, rs2995264, altering enhancer activity. The minor allele G of rs2995264 correlated with lower OBFC1 expression in 470 CMM tumors and was confirmed to increase the CMM risk in a cohort of 484 CMM cases and 1801 controls of Italian origin. Hi-C and chromosome conformation capture (3C) experiments showed the interaction between the enhancer-SNP region and the promoter of OBFC1 and an isogenic model characterized by CRISPR-Cas9 deletion of the enhancer-SNP region confirmed the potential regulatory effect of rs2995264 on OBFC1 transcription. Moreover, the presence of G-rs2995264 risk allele reduced the binding affinity of the transcription factor MEOX2. Biologic investigations showed significant cell viability upon depletion of OBFC1, specifically in CMM cells that were homozygous for the protective allele. Clinically, high levels of OBFC1 expression associated with histologically favorable CMM tumors. Finally, preliminary results suggested the potential effect of decreased OBFC1 expression on telomerase activity in tumorigenic conditions. Our results support the hypothesis that reduced expression of OBFC1 gene through functional heritable DNA variation can contribute to malignant transformation of normal melanocytes.
10q24.33 基因座已知与皮肤恶性黑色素瘤(CMM)易感性相关,但该关联的机制尚未得到广泛研究。我们使用表观基因组注释和体外报告基因检测进行了 10q24.33 的综合基因组分析,以鉴定调节变异。我们在神经嵴和 CMM 细胞中发现了 OBFC1 增强子和启动子中的两个假定功能性单核苷酸多态性(SNP),一个是 rs2995264,改变了增强子的活性。rs2995264 的次要等位基因 G 与 470 例 CMM 肿瘤中的 OBFC1 表达降低相关,并在意大利裔的 484 例 CMM 病例和 1801 例对照队列中证实了增加 CMM 风险的作用。Hi-C 和染色体构象捕获(3C)实验显示了增强子-SNP 区域与 OBFC1 启动子之间的相互作用,并且具有 CRISPR-Cas9 缺失增强子-SNP 区域的同基因模型证实了 rs2995264 对 OBFC1 转录的潜在调节作用。此外,G-rs2995264 风险等位基因的存在降低了转录因子 MEOX2 的结合亲和力。生物学研究表明 OBFC1 缺失后细胞活力显著降低,特别是在保护性等位基因纯合的 CMM 细胞中。临床上,OBFC1 表达水平高与组织学上有利的 CMM 肿瘤相关。最后,初步结果表明降低 OBFC1 表达对肿瘤发生条件下端粒酶活性的潜在影响。我们的研究结果支持这样一种假设,即通过功能可遗传的 DNA 变异降低 OBFC1 基因的表达可能有助于正常黑素细胞的恶性转化。