https://scholars.lib.ntu.edu.tw/handle/123456789/547861
標題: | Rapid detection of β-globin gene (HBB) mutations coupling heteroduplex and primer-extension analysis by DHPLC | 作者: | Su Y.-N. CHIEN-NAN LEE Hung C.-C. CHI-AN CHEN WEN-FANG CHENG PO-NIEN TSAO CHIA-LI YU FON-JOU HSIEH |
公開日期: | 2003 | 卷: | 22 | 期: | 4 | 起(迄)頁: | 326-336 | 來源出版物: | Human Mutation | 摘要: | Beta-thalassemia is a common inherited disease, resulting from one or more of a total of more than 200 different mutations in the β-globin gene (HBB). Efficient and reliable mutation-screening methods are essential in order to establish appropriate prevention programs for at-risk populations based upon a molecular diagnosis. We have developed a rapid and highly-specific mutation screening test for the diagnosis of β-thalassemia by coupling heteroduplex and primer-extension analysis based on the denaturing high performance liquid chromatography (DHPLC) system. A total of 161 healthy heterozygous Taiwanese carriers featuring 10 different HBB mutations and 30 patients exhibiting 12 different compound heterozygous or homozygous HBB mutations were subjected to DHPLC. The elution profile for the heteroduplex analysis of DHPLC could be successfully used to identify the common disease-causing mutations of HBB. To further confirm the sequence variants, we developed a technique combining multiplex primer-extension analysis coupled with DHPLC for the genotyping of eight common disease-causing mutations in the HBB gene. Overall, by coupling heteroduplex and primer-extension analysis based upon DHPLC, we were able to unambiguously identify the most-common β-thalassemia mutations corresponding to more than 99% of HBB alleles among the Taiwanese population. In conclusion, compared to classic approaches to mutation screening for this malady, we suggest that DHPLC is an excellent technique to be applied to the genetic screening of prenatal and postnatal individuals as a part of a diagnosis program for β-thalassemia and provides a more-efficient, economic, and sensitive means to undertake such a screening program. ? 2003 Wiley-Liss, Inc. |
URI: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-0141642025&doi=10.1002%2fhumu.10265&partnerID=40&md5=ba82b0bede84e03495d78de9a0b4cd1c https://scholars.lib.ntu.edu.tw/handle/123456789/547861 |
ISSN: | 1059-7794 | DOI: | 10.1002/humu.10265 | SDG/關鍵字: | beta globin; heteroduplex; primer DNA; allele; article; beta thalassemia; denaturing high performance liquid chromatography; diagnostic accuracy; diagnostic value; DNA denaturation; elution; gene mutation; gene sequence; genetic screening; heterozygote; high performance liquid chromatography; homozygosity; human; mutational analysis; nucleotide sequence; priority journal; screening test; sequence analysis; Taiwan; Base Sequence; beta-Thalassemia; Chromatography, High Pressure Liquid; DNA Mutational Analysis; Genetic Screening; Globins; Heteroduplex Analysis; Humans; Molecular Sequence Data; Mutation; Polymerase Chain Reaction; Time Factors |
顯示於: | 醫學系 |
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