Department of Genetic Medicine, St Mary's Hospital, Manchester Academic Health Sciences Centre, University of Manchester, Manchester, UK.
Oncogene. 2010 Nov 25;29(47):6216-21. doi: 10.1038/onc.2010.363. Epub 2010 Aug 23.
Biallelic inactivation of the NF2 gene occurs in the majority of schwannomas. This usually involves a combination of a point mutation or multiexon deletion, in conjunction with either a second point mutation or loss of heterozygosity (LOH). We have performed DNA sequence and dosage analysis of the NF2 gene in a panel of 239 schwannoma tumours: 97 neurofibromatosis type 2 (NF2)-related schwannomas, 104 sporadic vestibular schwannomas (VS) and 38 schwannomatosis-related schwannomas. In total, we identified germline NF2 mutations in 86 out of 97 (89%) NF2 patients and a second mutational event in 77 out of 97 (79%). LOH was by far the most common form of second hit. A combination of microsatellite analysis with either conventional comparative genomic hybridization (CGH) or multiplex ligation-dependent probe amplification (MLPA) identified mitotic recombination (MR) as the cause of LOH in 14 out of 72 (19%) total evaluable tumours. Among sporadic VS, at least one NF2 mutation was identified by sequence analysis or MLPA in 65 out of 98 (66%) tumours. LOH occurred in 54 out of 96 (56%) evaluable tumours, but MR only accounted for 5 out of 77 (6%) tested. LOH was present in 28 out of 34 (82%) schwannomatosis-related schwannomas. In all eight patients who had previously tested positive for a germline SMARCB1 mutation, this involved loss of the whole, or part of the long arm, of chromosome 22. In contrast, 5 out of 22 (23%) tumours from patients with no germline SMARCB1 mutation exhibited MR. High-resolution Affymetrix SNP6 genotyping and copy number (CN) analysis (Affymetrix, Santa Clara, CA, USA) were used to determine the chromosomal breakpoint locations in tumours with MR. A range of unique recombination sites, spanning approximately 11.4 Mb, were identified. This study shows that MR is a mechanism of LOH in NF2 and SMARCB1-negative schwannomatosis-related schwannomas, occurring less frequently in sporadic VS. We found no evidence of MR in SMARCB1-positive schwannomatosis, suggesting that susceptibility to MR varies according to the disease context.
NF2 基因的双等位基因失活发生在大多数神经鞘瘤中。这通常涉及点突变或外显子缺失的组合,同时伴有第二个点突变或杂合性丢失 (LOH)。我们对 239 例神经鞘瘤肿瘤的 NF2 基因进行了 DNA 序列和剂量分析:97 例神经纤维瘤病 2 型 (NF2) 相关神经鞘瘤、104 例散发性前庭神经鞘瘤 (VS) 和 38 例神经鞘瘤病相关神经鞘瘤。总共在 97 例 NF2 患者中的 86 例 (89%) 发现了种系 NF2 突变,在 97 例中的 77 例 (79%) 发现了第二个突变事件。LOH 是最常见的二次打击形式。微卫星分析与传统比较基因组杂交 (CGH) 或多重连接依赖性探针扩增 (MLPA) 的组合鉴定有丝分裂重组 (MR) 为 72 个可评估肿瘤中 14 个 (19%) 的 LOH 原因。在散发性 VS 中,通过序列分析或 MLPA 在 98 个中的 65 个 (66%) 肿瘤中发现至少一个 NF2 突变。在 96 个可评估肿瘤中有 54 个 (56%) 发生 LOH,但仅在 77 个中的 5 个 (6%) 进行了 MR。在 34 个神经鞘瘤病相关神经鞘瘤中有 28 个 (82%) 存在 LOH。在之前检测到种系 SMARCB1 突变阳性的所有 8 名患者中,这涉及整条或 22 号染色体长臂的部分缺失。相比之下,在没有种系 SMARCB1 突变的 22 个肿瘤中,有 5 个表现出 MR。使用高分辨率 Affymetrix SNP6 基因分型和拷贝数 (CN) 分析 (Affymetrix,圣克拉拉,CA,美国) 来确定具有 MR 的肿瘤中的染色体断裂点位置。确定了一系列独特的重组位点,跨度约为 11.4Mb。这项研究表明,MR 是 NF2 和 SMARCB1 阴性神经鞘瘤病相关神经鞘瘤中 LOH 的一种机制,在散发性 VS 中发生频率较低。我们没有发现 MR 在 SMARCB1 阳性神经鞘瘤病中的证据,这表明 MR 的易感性根据疾病背景而有所不同。