Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10

Tohru Matsuura, Ping Fang, Xi Lin, Mehrdad Khajavi, Kuniko Tsuji, Astrid Rasmussen, Raji P. Grewal, Madhureeta Achari, Maria F. Alonso, Stefan M. Pulst, Huda Y. Zoghbi, David L. Nelson, Benjamin B. Roa, Tetsuo Ashizawa

Research output: Contribution to journalArticle

50 Scopus citations

Abstract

Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant disorder characterized by ataxia, seizures, and anticipation. It is caused by an expanded ATTCT pentanucleotide repeat in intron 9 of a novel gene, designated "SCA10." The ATTCT expansion in SCA10 represents a novel class of microsatellite repeat and is one of the largest found to cause human diseases. The expanded ATTCT repeat is unstably transmitted from generation to generation, and an inverse correlation has been observed between size of repeat and age at onset. In this multifamily study, we investigated the intergenerational instability, somatic and germline mosaicism, and age-dependent repeat-size changes of the expanded ATTCT repeat. Our results showed that (1) the expanded ATTCT repeats are highly unstable when paternally transmitted, whereas maternal transmission resulted in significantly smaller changes in repeat size; (2) blood leukocytes, lymphoblastoid cells, buccal cells, and sperm have a variable degree of mosaicism in ATTCT expansion; (3) the length of the expanded repeat was not observed to change in individuals over a 5-year period; and (4) clinically determined anticipation is sometimes associated with intergenerational contraction rather than expansion of the ATTCT repeat.

Original languageEnglish (US)
Pages (from-to)1216-1224
Number of pages9
JournalAmerican Journal of Human Genetics
Volume74
Issue number6
DOIs
StatePublished - Jun 2004

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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