Molecular Characterization of the NF2 Gene in Korean Patients with Neurofibromatosis Type 2: A Report of Four Novel Mutations

作者：Seong Moon Woo; Yeo Im Kyung; Cho Sung Im; Park Chul Kee; Kim Seung Ki; Paek Sun Ha; Kim Dong Gyu; Jung Hee Won; Park Hyunwoong; Kim So Yeon; Kim Ji Yeon; Park Sung Sup^*

来源：Korean Journal of Laboratory Medicine, 2010, 30(2): 190-194.

DOI：10.3343/kjlm.2010.30.2.190

• Hereditary cancer
• Neurofibromatosis type 2
• NF2

Background : Neurofibromatosis type 2 (NF2) is an autosomal dominant syndrome caused by the NF2 tumor suppressor gene. However, the NF2 mutation characteristics in Korean patients are not sufficiently understood. In this study, we conducted a comprehensive mutational analysis in 7 Korean NF2 patients by performing direct sequencing and gene-dosage assessment.
Methods : We analyzed all exons and flanking regions of NF2 by direct sequencing and screened the deletions or duplications involving NF2 by multiplex ligation-dependent probe amplification.
Results : Four novel NF2 mutations, including 2 splice-site mutations (c.364-1G>A and c.886-3C>G), 1 frameshift mutation (c.524delA), and 1 missense mutation (c.3971>C; p.Cys133Arg), were identified in our patients. No large deletion or duplication was identified in our series. Subsequently, we identified an abnormal splicing product by using reverse transcription-PCR and direct sequencing in 2 patients with a novel splice-site mutation. The missense mutation c.397T>C was predicted to have harmful effects on protein function.
Conclusions : The detection rate of NF2 mutations in Korean patients (57%) is similar to those in other populations. Our results provided a greater insight into the mutational spectrum of the NF2 gene in Korean subjects. (Korean J Lab Med 2010;30:190-4)

• 出版日期2010-4