Section for Cancer Cytogenetics, Institute for Cancer Genetics and Informatics, the Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway
Section for Cancer Cytogenetics, Institute for Cancer Genetics and Informatics, the Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway.
Cancer Genomics Proteomics. 2020 Sep-Oct;17(5):555-561. doi: 10.21873/cgp.20211.
BACKGROUND/AIM: Aneurysmal bone cyst is a benign bone lesion with a strong tendency to recur. The rearrangement of chromosome band 17p13/USP6 gene is now considered a characteristic genetic feature of aneurysmal bone cyst, with t(16;17)(q22;p13)/CDH11-USP6 as the most frequent chromosomal aberration/fusion gene. We report a novel variant translocation leading to a new fusion gene in an aneurysmal bone cyst.
Genetic analyses were performed on an aneurysmal bone cyst found in the tibia of a child.
G-banding chromosome analysis yielded the karyotype 46,XX,t(12;17)(q21;p13)[5]/46,XX[2]. FISH analysis with a USP6 break-apart probe showed rearrangement of USP6. RNA sequencing detected LUM-USP6 and USP6-LUM fusion transcripts which were subsequently verified by RT-PCR/Sanger sequencing. The two genes exchanged 5'- non-coding exons. Thus, promoter swapping between USP6 and LUM had taken place.
We report a novel t(12;17)(q21;p13) chromosome translocation which gave rise to a LUM-USP6 fusion in an aneurysmal bone cyst.
背景/目的:动脉瘤样骨囊肿是一种具有强烈复发倾向的良性骨病变。现在认为染色体 17p13/USP6 基因重排是动脉瘤样骨囊肿的一个特征性遗传特征,t(16;17)(q22;p13)/CDH11-USP6 是最常见的染色体异常/融合基因。我们报告了一种导致动脉瘤样骨囊肿中出现新融合基因的新型变体易位。
对儿童胫骨中的动脉瘤样骨囊肿进行了遗传分析。
G 带染色体分析得到的核型为 46,XX,t(12;17)(q21;p13)[5]/46,XX[2]。USP6 断裂探针的 FISH 分析显示 USP6 重排。RNA 测序检测到 LUM-USP6 和 USP6-LUM 融合转录本,随后通过 RT-PCR/Sanger 测序进行了验证。这两个基因交换了 5'-非编码外显子。因此,USP6 和 LUM 之间发生了启动子交换。
我们报告了一种新的 t(12;17)(q21;p13)染色体易位,导致动脉瘤样骨囊肿中出现 LUM-USP6 融合。