Association between metallothionein genes polymorphisms and sporadic amyotrophic lateral sclerosis in a Japanese population

Amyotrophic lateral sclerosis (ALS) is a progressive, lethal neurodegenerative disease that selectively affects motor neurons. Reactive oxygen species (ROS) are assumed to be involved in the pathogenesis of ALS. Metallothioneins (MTs) are self-protective, multifunctional proteins that scavenge ROS....

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Veröffentlicht in:Amyotrophic lateral sclerosis 2006-03, Vol.7 (1), p.22-26
Hauptverfasser: Hayashi, Yuichi, Hashizume, Tatsuma, Wakida, Kenji, Satoh, Masahiko, Uchida, Yoko, Watabe, Kazuhiko, Matsuyama, Zenjiro, Kimura, Akio, Inuzuka, Takashi, Hozumi, Isao
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Sprache:eng
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Zusammenfassung:Amyotrophic lateral sclerosis (ALS) is a progressive, lethal neurodegenerative disease that selectively affects motor neurons. Reactive oxygen species (ROS) are assumed to be involved in the pathogenesis of ALS. Metallothioneins (MTs) are self-protective, multifunctional proteins that scavenge ROS. In particular, metallothionein-III (MT-III) has a strong scavenging effect on hydroxyl radicals. MTs have been suggested to have important roles in the pathophysiology of ALS. Therefore we investigated single nucleotide polymorphisms (SNPs) of the MT-III and the metallothionein-IIA (MT-IIA) promoter region in 37 Japanese SALS cases and 206 sex-matched healthy controls using polymerase chain reaction (PCR)-direct sequencing or PCR-temporal temperature gradient gel electrophoresis (TTGE). We detected no SNPs of the MT-III gene in SALS cases and controls, and no detectable association between SALS phenotypes and a SNP of the MT-IIA promoter region. We conclude that gene polymorphisms of MT-IIA promoter region and MT-III gene are not associated with SALS phenotypes in a Japanese population.
ISSN:1748-2968
1466-0822
1471-180X
DOI:10.1080/14660820600618766