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KMID : 1189120130100010033
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대한의학유전학회지
2013 Volume.10 No. 1 p.33 ~ p.37
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Southern Analysis after Long-range PCR: Clinical Application in Korean Patients with Myotonic Dystrophy 1
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Yum Mi-Sun
Lee Beom-Hee
Kim Gu-Hwan
Lee Jin-Joo
Choi Seung-Hoon
Lee Joo-Yeon
Kim Jae-Min
Kim Yoo-Mi
Ko Tae-Sung
Yoo Han-Wook
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Abstract
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Purpose: Myotonic dystrophy 1 (DM1, OMIM 160900) is an autosomal-dominant muscular disorder caused by an expansion of CTG repeats in the 3’ UTR of the DMPK gene. Variable expansions of CTG repeats preclude the accurate determination of repeat size. We tried to show the clinical and analytical validity of the application of Southern blotting after long-range PCR was demonstrated in Korean DM1 patients.
Materials and Methods: The Southern blotting of long-range PCR was applied to 1,231 cases with clinical suspicion of DM1, between 2000 and 2011. PCR was performed using genomic DNA with forward 5’-CAGTTCACAACCGCTCCGAGC-3’ and reverse 5’-CGTGGAGGATGGAACACGGAC-3’ primers. Subsequently, the PCR fragments were subjected to gel electrophoresis, capillary transfer to a nylon membrane, hybridization with a labeled (CAG)10 probe. The correlation between clinical manifestations and the CTG repeat expansions were analyzed.
Results: Among a total of 1,231 tested cases, 642 individuals were diagnosed with DM1 and the range of the detected expansion was 50 to 2,500 repeats; fourteen cases with mild DM1 (75±14 repeats), 602 cases with classical DM1 (314±143 repeats), and 26 cases with congenital DM1 (1,219±402 repeats). The positive and negative predictive values were 100%. The age at tes requested and the CTG repeat numbers were inversely correlated (R=-0.444, P<0.01).
Conclusion: This study indicates that Southern blotting after long-range PCR is a reliable diagnostic method DM1.
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KEYWORD
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Myotonic dystrophy 1, Southern blotting, Long-range PCR, Genetic testing
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