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A novel mutation at position +12 in the intron following Exon 10 of the tau gene in familial frontotemporal dementia (FTD‐Kumamoto)
Author(s) -
Yasuda Minoru,
Takamatsu Junichi,
D'Souza Ian,
Crowther R. Anthony,
Kawamata Toshio,
Hasegawa Masato,
Hasegawa Hiroshi,
Grazia Spillantini Maria,
Tanimukai Satoshi,
Poorkaj Parvoneh,
Varani Luca,
Varani Gabriele,
Iwatsubo Takeshi,
Goedert Michel,
Schellenberg Gerard D.,
Tanaka Chikako
Publication year - 2000
Publication title -
annals of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.764
H-Index - 296
eISSN - 1531-8249
pISSN - 0364-5134
DOI - 10.1002/1531-8249(200004)47:4<422::aid-ana4>3.0.co;2-g
Subject(s) - frontotemporal dementia , exon , genetics , mutation , intron , dementia , gene , medicine , psychology , biology , disease
Exonic and intronic mutations in the tau gene cause familial frontotemporal dementia and parkinsonism linked to chromosome 17. Here, we describe a new mutation, consisting of a C‐to‐T transition at position +12 of the intron following exon 10 of the tau gene in the Kumamoto pedigree, showing frontotemporal dementia. The mutation caused a marked reduction in melting temperature of the tau exon 10–splicing regulatory element RNA and a large increase in exon 10–containing transcripts. Brain tissue from affected individuals showed an abnormal preponderance of exon 10–containing transcripts that was reflected at the protein level by an overproduction of tau isoforms with four microtubule‐binding repeats. Immunostaining revealed the presence of tau aggregates in degenerating neurons and glial cells. Isolated tau filaments had a twisted ribbon‐like morphology and were made of hyperphosphorylated four‐repeat tau isoforms. The additional mutation located close to the splice‐donor site of the intron following exon 10 of the tau gene supports the view that intronic mutations exercize their pathogenic effect by destabilizing RNA secondary structure. Ann Neurol 2000;47:422–429.