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The (CAG)n tract of Machado-Joseph Disease gene (ATXN3): a comparison between DNA and mRNA in patients and controls
被引:18
|作者:
Bettencourt, Conceicao
[1
,2
,3
]
Santos, Cristina
[1
,2
,4
]
Montiel, Rafael
[5
]
Kay, Teresa
[6
]
Vasconcelos, Joao
[7
]
Maciel, Patricia
[8
]
Lima, Manuela
[1
,2
,3
]
机构:
[1] Univ Azores, Ctr Res Nat Resources CIRN, P-9501801 Ponta Delgada, Azores, Portugal
[2] Univ Azores, Dept Biol, P-9501801 Ponta Delgada, Azores, Portugal
[3] Univ Porto, IBMC, P-4100 Oporto, Portugal
[4] Univ Autonoma Barcelona, Unitat Antropol Biol, Dep Biol Anim Biol Vegetal & Ecol, E-08193 Barcelona, Spain
[5] CINVESTAV IPN, Lab Nacl Genom Biodiversidad, Irapuato, Mexico
[6] Hosp D Estefania, Dept Clin Genet, Lisbon, Portugal
[7] Hosp Divino Espirito Santo, Dept Neurol, Ponta Delgada, Portugal
[8] Univ Minho, Sch Hlth Sci, Life & Hlth Sci Res Inst ICVS, Braga, Portugal
关键词:
MJD;
SCA3;
CAG repeats;
transcript variation;
polyglutamine disorders;
CLINICAL-FEATURES;
SOMATIC MOSAICISM;
AZORES ISLANDS;
REPEAT;
CEREBELLAR;
FAMILIES;
SYSTEM;
MJD;
D O I:
10.1038/ejhg.2009.215
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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 (similar to 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. European Journal of Human Genetics (2010) 18, 621-623; doi:10.1038/ejhg.2009.215; published online 25 November 2009
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页码:621 / 623
页数:3
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