Circulation journal : official journal of the Japanese Circulation Society · 2004
Genetic analysis of Brugada syndrome in Western Japan: two novel mutations.
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Niimura Hideya, Matsunaga Akira, Kumagai Koichiro, Ohwaki Kazuo, Ogawa Masahiro, Noguchi Hiroo, Yonemura Kazue, Saku Keijiro
Аннотация
BACKGROUND: Brugada syndrome is a form of idiopathic ventricular fibrillation characterized by right bundle-branch block pattern and ST elevation in the right precordial leads of the ECG. The SCN5A gene encodes the alpha-subunit of the human heart sodium channel, which plays a critical role in cardiac excitability, and mutations of SCN5A could underlie Brugada syndrome.
METHODS AND RESULTS: To detect mutations of SCN5A, DNA samples from 12 Japanese patients with Brugada syndrome were analyzed using direct sequencing. Two patients had novel mutations, G292S and S835L, but no other mutations of SCN5A were detected in the remaining patients. The first mutation, G292S, was identified adjacent to the pore-lining region between the DIS5 and DIS6 transmembrane segments of SCN5A, and the second mutation, S835L, was in the intracellular loop connecting the DIIS4 to DIIS5. Both mutations were not detected in 100 unrelated control subjects.
CONCLUSION: Two novel SCN5A mutations have been found in Japanese patients with Brugada syndrome.
METHODS AND RESULTS: To detect mutations of SCN5A, DNA samples from 12 Japanese patients with Brugada syndrome were analyzed using direct sequencing. Two patients had novel mutations, G292S and S835L, but no other mutations of SCN5A were detected in the remaining patients. The first mutation, G292S, was identified adjacent to the pore-lining region between the DIS5 and DIS6 transmembrane segments of SCN5A, and the second mutation, S835L, was in the intracellular loop connecting the DIIS4 to DIIS5. Both mutations were not detected in 100 unrelated control subjects.
CONCLUSION: Two novel SCN5A mutations have been found in Japanese patients with Brugada syndrome.
Предметные рубрики MeSH
AdultAgedBase SequenceBundle-Branch BlockFemaleHumansJapanMaleMiddle AgedModels, MolecularMutagenesis, Site-DirectedMutation, MissenseNAV1.5 Voltage-Gated Sodium ChannelPedigreePolymorphism, Restriction Fragment LengthProtein ConformationRecombinant ProteinsReverse Transcriptase Polymerase Chain ReactionSodium Channels