Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/67531

TitleIncreased transcript diversity: novel splicing variants of Machado-Joseph disease gene (ATXN3)
Author(s)Bettencourt, Conceição
Santos, Cristina
Montiel, Rafael
Costa, Maria do Carmo
Cruz-Morales, Pablo
Santos, Liliana Ribeiro
Simões, Nelson
Kay, Teresa
Vasconcelos, João
Maciel, P.
Lima, Manuela
KeywordsAtaxin-3
Base sequence
Humans
Machado-Joseph disease
Models, Molecular
Molecular sequence data
Nerve tissue proteins
Nuclear proteins
Protein conformation
Repressor proteins
Alternative splicing
MJD
SCA3
Transcript variants
PolyQ disorders
Issue date2010
PublisherSpringer
JournalNeurogenetics
Abstract(s)Machado-Joseph disease (MJD) is a late-onset neurodegenerative disorder that presents clinical heterogeneity not completely explained by its causative mutation. MJD is caused by an expansion of a CAG tract at exon 10 of the ATXN3 gene (14q32.1), which encodes for ataxin-3. The main goal of this study was to analyze the occurrence of alternative splicing at the ATXN3 gene, by sequencing a total of 415 cDNAs clones (from 20 MJD patients and 14 controls). Two novel exons are described for the ATXN3 gene. Fifty-six alternative splicing variants, generated by four types of splicing events, were observed. From those variants, 50 were not previously described, and 26 were only found in MJD patients samples. Most of the variants (85.7%) present frameshift, which leads to the appearance of premature stop codons. Thirty-seven of the observed variants constitute good targets to nonsense-mediated decay, the remaining are likely to be translated into at least 20 different isoforms. The presence of ataxin-3 domains was assessed, and consequences of domain disruption are discussed. The present study demonstrates high variability in the ATXN3 gene transcripts, providing a basis for further investigation on the contribution of alternative splicing to the MJD pathogenic process, as well as to the larger group of the polyglutamine disorders.
TypeArticle
URIhttp://hdl.handle.net/1822/67531
DOI10.1007/s10048-009-0216-y
ISSN1364-6745
e-ISSN1364-6753
Publisher versionhttps://link.springer.com/article/10.1007/s10048-009-0216-y
Peer-Reviewedyes
AccessRestricted access (UMinho)
Appears in Collections:ICVS - Artigos em revistas internacionais / Papers in international journals

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