TY - JOUR
T1 - The (CAG)n tract of Machado-Joseph Disease gene (ATXN3)
T2 - A comparison between DNA and mRNA in patients and controls
AU - Bettencourt, Conceiço
AU - Santos, Cristina
AU - Montiel, Rafael
AU - Kay, Teresa
AU - Vasconcelos, Joo
AU - MacIel, Patrícia
AU - Lima, Manuela
N1 - Funding Information:
This work was supported by projects ‘PRI-DMJ’ (funded by the Regional Government of the Azores) and ‘Transcriptional variation of the ATXN3 gene as modulator of the clinical heterogeneity in Machado–Joseph disease (MJD)’ (PIC/IC/83074/2007, funded by ‘Fundac¸ão para a Ciência e a Tecnologia’ – FCT). CB (SFRH/BD/21875/2005) is the recipient of a PhD grant from FCT.
Copyright:
Copyright 2010 Elsevier B.V., All rights reserved.
PY - 2010/5/1
Y1 - 2010/5/1
N2 - Machado-Joseph disease (MJD) is an autosomal dominant neurodegenerative disorder of late onset (occurring at a mean age of 40.2 years). The clinical manifestation of MJD is dependent on the presence of an expansion of the (CAG)n motif within exon 10 of the ATXN3 gene, located at 14q32.1. The variance in onset of MJD is only partially correlated (∼ 50-80%) with the extension of the CAG tract in genomic DNA (gDNA). The main aim of this work was to determine whether there are discrepancies in the size of the (CAG) n tract between gDNA and mRNA, and to establish whether there is a better association between age at onset and repeat size at the mRNA level. We typed gDNA and cDNA samples for the (CAG)n tract totalizing 108 wild-type and 52 expanded ATXN3 alleles. In wild-type alleles no differences were found between gDNA and cDNA. In expanded alleles, the CAG repeat size in gDNA was not always directly transcribed into the mRNA; on average there were differences of 1 repeat at the cDNA level. The slight discrepancies obtained were insufficient to cause significant differences in the distribution of the expanded alleles, and therefore no improvement in onset variance explanation was obtained with mRNA. © 2010 Macmillan Publishers Limited All rights reserved.
AB - Machado-Joseph disease (MJD) is an autosomal dominant neurodegenerative disorder of late onset (occurring at a mean age of 40.2 years). The clinical manifestation of MJD is dependent on the presence of an expansion of the (CAG)n motif within exon 10 of the ATXN3 gene, located at 14q32.1. The variance in onset of MJD is only partially correlated (∼ 50-80%) with the extension of the CAG tract in genomic DNA (gDNA). The main aim of this work was to determine whether there are discrepancies in the size of the (CAG) n tract between gDNA and mRNA, and to establish whether there is a better association between age at onset and repeat size at the mRNA level. We typed gDNA and cDNA samples for the (CAG)n tract totalizing 108 wild-type and 52 expanded ATXN3 alleles. In wild-type alleles no differences were found between gDNA and cDNA. In expanded alleles, the CAG repeat size in gDNA was not always directly transcribed into the mRNA; on average there were differences of 1 repeat at the cDNA level. The slight discrepancies obtained were insufficient to cause significant differences in the distribution of the expanded alleles, and therefore no improvement in onset variance explanation was obtained with mRNA. © 2010 Macmillan Publishers Limited All rights reserved.
KW - CAG repeats
KW - MJD
KW - Polyglutamine disorders
KW - SCA3
KW - Transcript variation
UR - http://www.scopus.com/inward/record.url?scp=77951621418&partnerID=8YFLogxK
U2 - 10.1038/ejhg.2009.215
DO - 10.1038/ejhg.2009.215
M3 - Article
C2 - 19935829
SN - 1018-4813
VL - 18
SP - 621
EP - 623
JO - European Journal of Human Genetics
JF - European Journal of Human Genetics
IS - 5
ER -