Southern Analysis after Long-range PCR: Clinical Application in Korean Patients with Myotonic Dystrophy 1.
- Author:
Mi Sun YUM
1
;
Beom Hee LEE
;
Gu Hwan KIM
;
Jin Joo LEE
;
Seung Hoon CHOI
;
Joo Yeon LEE
;
Jae Min KIM
;
Yoo Mi KIM
;
Tae Sung KO
;
Han Wook YOO
Author Information
- Publication Type:Original Article
- Keywords: Myotonic dystrophy 1; Southern blotting; Long-range PCR; Genetic testing
- MeSH: 3' Untranslated Regions; Blotting, Southern; Chimera; Databases, Genetic; DNA; Electrophoresis, Capillary; Genetic Testing; Humans; Membranes; Myotonic Dystrophy; Nylons; Polymerase Chain Reaction
- From:Journal of Genetic Medicine 2013;10(1):33-37
- CountryRepublic of Korea
- Language:English
- Abstract: 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 test 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.
