Suppr超能文献

功能注释和对 10q24.33 黑色素瘤风险位点的研究确定了一个常见的变异,该变异影响 OBFC1 的转录调控。

Functional annotation and investigation of the 10q24.33 melanoma risk locus identifies a common variant that influences transcriptional regulation of OBFC1.

机构信息

Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli Federico II, Naples 80136, Italy.

CEINGE Biotecnologie Avanzate, Naples 80145, Italy.

出版信息

Hum Mol Genet. 2022 Mar 21;31(6):863-874. doi: 10.1093/hmg/ddab293.

Abstract

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.

摘要

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。

相似文献

3
Multiple Functional Variants at 13q14 Risk Locus for Osteoporosis Regulate RANKL Expression Through Long-Range Super-Enhancer.
J Bone Miner Res. 2018 Jul;33(7):1335-1346. doi: 10.1002/jbmr.3419. Epub 2018 May 17.
7
Cytokine gene single nucleotide polymorphisms and susceptibility to and prognosis in cutaneous malignant melanoma.
Eur J Immunogenet. 2003 Dec;30(6):409-14. doi: 10.1111/j.1365-2370.2003.00425.x.
8
Polymorphisms in the syntaxin 17 gene are not associated with human cutaneous malignant melanoma.
Melanoma Res. 2009 Apr;19(2):80-6. doi: 10.1097/CMR.0b013e328322fc45.
9
Association of XPC Polymorphisms with Cutaneous Malignant Melanoma Risk: Evidence from a Meta-Analysis.
Acta Medica (Hradec Kralove). 2020;63(3):101-112. doi: 10.14712/18059694.2020.27.
10
Identification of an enhancer region within the TP63/LEPREL1 locus containing genetic variants associated with bladder cancer risk.
Cell Oncol (Dordr). 2018 Oct;41(5):555-568. doi: 10.1007/s13402-018-0393-5. Epub 2018 Jun 28.

本文引用的文献

1
Germline ATM variants predispose to melanoma: a joint analysis across the GenoMEL and MelaNostrum consortia.
Genet Med. 2021 Nov;23(11):2087-2095. doi: 10.1038/s41436-021-01240-8. Epub 2021 Jul 14.
3
Evolution of approaches to identify melanoma missing heritability.
Expert Rev Mol Diagn. 2020 May;20(5):523-531. doi: 10.1080/14737159.2020.1738221. Epub 2020 Mar 14.
5
Benefits and limitations of genome-wide association studies.
Nat Rev Genet. 2019 Aug;20(8):467-484. doi: 10.1038/s41576-019-0127-1.
6
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways.
Nat Commun. 2018 Nov 14;9(1):4774. doi: 10.1038/s41467-018-06649-5.
7
Over-expression of MEOX2 promotes apoptosis through inhibiting the PI3K/Akt pathway in laryngeal cancer cells.
Neoplasma. 2018 Sep 19;65(5):745-752. doi: 10.4149/neo_2018_171218N824. Epub 2018 Jun 18.
8
CRISPOR: intuitive guide selection for CRISPR/Cas9 genome editing experiments and screens.
Nucleic Acids Res. 2018 Jul 2;46(W1):W242-W245. doi: 10.1093/nar/gky354.
9
Genome-wide association studies of cancer: current insights and future perspectives.
Nat Rev Cancer. 2017 Nov;17(11):692-704. doi: 10.1038/nrc.2017.82. Epub 2017 Oct 13.
10
A common intronic variant of PARP1 confers melanoma risk and mediates melanocyte growth via regulation of MITF.
Nat Genet. 2017 Sep;49(9):1326-1335. doi: 10.1038/ng.3927. Epub 2017 Jul 31.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验