Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.

TitleLarge expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.
Publication TypeJournal Article
Year of Publication2000
AuthorsMatsuura, T, Yamagata, T, Burgess, DL, Rasmussen, A, Grewal, RP, Watase, K, Khajavi, M, McCall, AE, Davis, CF, Zu, L, Achari, M, Pulst, SM, Alonso, E, Noebels, JL, Nelson, DL, Zoghbi, HY, Ashizawa, T
JournalNat Genet
Volume26
Issue2
Pagination191-4
Date Published2000 Oct
ISSN1061-4036
KeywordsAnimals, Asian Continental Ancestry Group, Brain, Chromosome Mapping, Chromosomes, Human, Pair 22, DNA, Epilepsy, European Continental Ancestry Group, Female, Humans, Male, Mexican Americans, Mice, Mice, Inbred C57BL, Molecular Sequence Data, Pedigree, Polymorphism, Genetic, Repetitive Sequences, Nucleic Acid, Spinocerebellar Ataxias, United States
Abstract

Spinocerebellar ataxia type 10 (SCA10; MIM 603516; refs 1,2) is an autosomal dominant disorder characterized by cerebellar ataxia and seizures. The gene SCA10 maps to a 3.8-cM interval on human chromosome 22q13-qter (refs 1,2). Because several other SCA subtypes show trinucleotide repeat expansions, we examined microsatellites in this region. We found an expansion of a pentanucleotide (ATTCT) repeat in intron 9 of SCA10 in all patients in five Mexican SCA10 families. There was an inverse correlation between the expansion size, up to 22.5 kb larger than the normal allele, and the age of onset (r2=0.34, P=0.018). Analysis of 562 chromosomes from unaffected individuals of various ethnic origins (including 242 chromosomes from Mexican persons) showed a range of 10 to 22 ATTCT repeats with no evidence of expansions. Our data indicate that the new SCA10 intronic ATTCT pentanucleotide repeat in SCA10 patients is unstable and represents the largest microsatellite expansion found so far in the human genome.

DOI10.1038/79911
Alternate JournalNat. Genet.
PubMed ID11017075
Grant ListHD24064 / HD / NICHD NIH HHS / United States
HD29256 / HD / NICHD NIH HHS / United States
NS27699 / NS / NINDS NIH HHS / United States