Analysis of β-thalassemia mutations in northern Thailand using an automated fluorescence DNA sequencing technique

• المؤلفون الرئيسيون: Sirichotiyakul S., Saetung R., Sanguansermsri T.
• التنسيق: مقال
• اللغة: English
• منشور في: 2014
• الوصول للمادة أونلاين: http://www.scopus.com/inward/record.url?eid=2-s2.0-0038585087&partnerID=40&md5=344940f77d9d465c2c7acfc47528a5c5; http://cmuir.cmu.ac.th/handle/6653943832/3181
• المؤسسة: Chiang Mai University

A total of 218 β-thalassemia (thal) genes from 109 β-thal major patients were characterized using an automated fluorescence DNA sequencing technique. Eight different mutations were identified in all 218 alleles (100%). Four common mutations accounted for 96.8% [49.5% were codons 41/42 (-TTCT), 34.4% were codon 17 (A→T), 6.9% were IVS-I-1 (G→T) and, 6.0% were codons 71/72 (+A)]. There were three cases of -28 (A→G) and one of IVS-II-654 (C→T), mutations that have been previously described in Thai subjects. We also identified two mutations in the β-globin promoter region which have not been reported in Thailand before [-31 (A→G) and -87 (C→A)]. Although these mutations are described as β+-thal, the compound heterozygote with one of the common β0-thal mutations exhibits the phenotype of β-thal major. The frequency of β-thal genes in northern Thailand were similar to the northeastern region, but different from those reported in southern and central Thailand, where IVS-I-5 (G→C) and IVS-II-654 (C→T) were the second most common anomalies, respectively. The spectrum of β-globin gene mutations from this study will be useful for planning a prenatal diagnosis program especially for this region of Thailand.