Department of Dermatology, RWTH Aachen University, Aachen, Germany.
Institute of Human Genetics, RWTH Aachen University, Aachen, Germany.
PLoS One. 2020 Mar 10;15(3):e0230003. doi: 10.1371/journal.pone.0230003. eCollection 2020.
Myotonic dystrophy type 1 (DM1) is an inherited neuromuscular disease which results from an expansion of repetitive DNA elements within the 3' untranslated region of the DMPK gene. Some patients develop multiple pilomatricomas as well as malignant tumors in other tissues. Mutations of the catenin-β gene (CTNNB1) could be demonstrated in most non-syndromic pilomatricomas. In order to gain insight into the molecular mechanisms which might be responsible for the occurrence of multiple pilomatricomas and cancers in patients with DM1, we have sequenced the CTNNB1 gene of four pilomatricomas and of one pilomatrical carcinoma which developed in one patient with molecularly proven DM1 within 4 years. We further analyzed the pilomatrical tumors for microsatellite instability as well as by NGS for mutations in 161 cancer-associated genes. Somatic and independent point-mutations were detected at typical hotspot regions of CTNNB1 (S33C, S33F, G34V, T41I) while one mutation within CTNNB1 represented a duplication mutation (G34dup.). Pilomatricoma samples were analyzed for microsatellite instability and expression of mismatch repair proteins but no mutated microsatellites could be detected and expression of mismatch repair proteins MLH1, MSH2, MSH6, PMS2 was not perturbed. NGS analysis only revealed one heterozygous germline mutation c.8494C>T; p.(Arg2832Cys) within the ataxia telangiectasia mutated gene (ATM) which remained heterozygous in the pilomatrical tumors. The detection of different somatic mutations in different pilomatricomas and in the pilomatrical carcinoma as well as the observation that the patient developed multiple pilomatricomas and one pilomatrical carcinoma over a short time period strongly suggest that the patient displays a hypermutation phenotype. This hypermutability seems to be tissue and gene restricted. Simultaneous transcription of the mutated DMPK gene and the CTNNB1 gene in cycling hair follicles might constitute an explanation for the observed tissue and gene specificity of hypermutability observed in DM1 patients. Elucidation of putative mechanisms responsible for hypermutability in DM1 patients requires further research.
1 型肌强直性营养不良(DM1)是一种遗传性神经肌肉疾病,由 DMPK 基因 3'非翻译区重复 DNA 元件的扩展引起。一些患者还会发展出多发性毛发基质瘤以及其他组织的恶性肿瘤。在大多数非综合征性毛发基质瘤中可以发现连环蛋白-β基因(CTNNB1)的突变。为了深入了解可能导致 DM1 患者多发性毛发基质瘤和癌症发生的分子机制,我们对来自一名分子确诊的 DM1 患者的 4 个毛发基质瘤和 1 个毛发基质癌的 CTNNB1 基因进行了测序,这些肿瘤在 4 年内发生。我们进一步分析了这些毛发基质瘤的微卫星不稳定性,以及通过 NGS 对 161 个癌症相关基因的突变进行了分析。在 CTNNB1 的典型热点区域(S33C、S33F、G34V、T41I)检测到了体细胞和独立的点突变,而 CTNNB1 内的一个突变代表了重复突变(G34dup.)。对毛发基质瘤样本进行了微卫星不稳定性分析和错配修复蛋白的表达分析,但未检测到突变的微卫星,错配修复蛋白 MLH1、MSH2、MSH6、PMS2 的表达也未受到干扰。NGS 分析仅在共济失调毛细血管扩张突变基因(ATM)中发现了一个杂合性胚系突变 c.8494C>T;p.(Arg2832Cys),该突变在毛发基质瘤中仍为杂合性。在不同的毛发基质瘤和毛发基质癌中检测到不同的体细胞突变,以及该患者在短时间内发展出多发性毛发基质瘤和 1 个毛发基质癌,强烈提示该患者表现出超突变表型。这种超突变似乎受到组织和基因的限制。在周期性的毛囊中同时转录突变的 DMPK 基因和 CTNNB1 基因,可能构成了 DM1 患者观察到的组织和基因特异性超突变的解释。阐明导致 DM1 患者超突变的潜在机制需要进一步研究。