Margraf Rebecca L, VanSant-Webb Chad, Sant David, Carey John, Hanson Heather, D'Astous Jacques, Viskochil Dave, Stevenson David A, Mao Rong
ARUP Institute for Clinical and Experimental Pathology, Salt Lake City, Utah.
ARUP Laboratories, Salt Lake City, Utah.
J Mol Diagn. 2017 May;19(3):468-474. doi: 10.1016/j.jmoldx.2017.01.008.
A subset of neurofibromatosis type 1 patients develop tibial dysplasia, which can lead to pseudarthrosis. The tissue from the tibial pseudarthrosis region commonly has a somatic second hit in NF1: single-nucleotide variants, small deletions, or loss of heterozygosity (LOH). We used exome next-generation sequencing (NGS) variant frequency data (allelic imbalance analysis) to detect somatic LOH in pseudarthrosis tissue from three individuals with clinically and diagnostically confirmed neurofibromatosis type 1, and verified the results with microarray. The variant files were parsed and plotted using python scripts, and the NGS variant frequencies between the affected tissue and blood sample were compared. Individuals without somatic single-nucleotide variants or small insertions/deletions were tested for somatic LOH using the NGS variant allele frequencies. One individual's NGS data indicated no LOH in chromosome 17. The other two individuals demonstrated somatic LOH inclusive of NF1: one had an LOH region of approximately one million bases and Contra (NGS copy number program) indicated a somatic deletion and the other individual had LOH for most of chromosome 17q and Contra indicated no copy number change (microarray data verified this sample as copy neutral somatic LOH). Both LOH and copy number variation detected by NGS data correlated with microarray data, demonstrating the somatic LOH second hit can be detected directly from the NGS data.
1型神经纤维瘤病患者的一个亚群会发生胫骨发育异常,这可能导致假关节形成。胫骨假关节区域的组织在NF1基因中通常存在体细胞二次打击:单核苷酸变异、小片段缺失或杂合性缺失(LOH)。我们使用外显子组下一代测序(NGS)变异频率数据(等位基因不平衡分析)来检测三名临床和诊断确诊为1型神经纤维瘤病患者的假关节组织中的体细胞LOH,并通过微阵列验证结果。使用python脚本解析和绘制变异文件,并比较受影响组织和血液样本之间的NGS变异频率。对于没有体细胞单核苷酸变异或小插入/缺失的个体,使用NGS变异等位基因频率检测体细胞LOH。一名个体的NGS数据表明17号染色体无LOH。另外两名个体表现出包含NF1基因的体细胞LOH:一名个体的LOH区域约为100万个碱基,Contra(NGS拷贝数程序)显示体细胞缺失,另一名个体17号染色体长臂的大部分区域存在LOH,Contra显示无拷贝数变化(微阵列数据验证该样本为拷贝中性体细胞LOH)。通过NGS数据检测到的LOH和拷贝数变异均与微阵列数据相关,表明可以直接从NGS数据中检测到体细胞LOH二次打击。