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马查多-约瑟夫病基因 (ATXN3) 的 (CAG)n 重复序列:患者和对照者的 DNA 和 mRNA 比较。

The (CAG)n tract of Machado-Joseph Disease gene (ATXN3): a comparison between DNA and mRNA in patients and controls.

机构信息

Center of Research in Natural Resources and Department of Biology, University of the Azores, Ponta Delgada, Portugal.

出版信息

Eur J Hum Genet. 2010 May;18(5):621-3. doi: 10.1038/ejhg.2009.215. Epub 2009 Nov 25.

Abstract

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 (approximately 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.

摘要

马查多-约瑟夫病(MJD)是一种常染色体显性遗传的神经退行性疾病,发病较晚(平均发病年龄为 40.2 岁)。MJD 的临床表现取决于 ATXN3 基因第 10 外显子中(CAG)(n)重复序列的扩展,该基因位于 14q32.1。MJD 的发病时间变异仅部分与基因组 DNA(gDNA)中 CAG 片段的延伸相关(约 50-80%)。本研究的主要目的是确定 gDNA 和 mRNA 中(CAG)(n)重复序列的大小是否存在差异,并确定在 mRNA 水平上,发病年龄与重复大小之间是否存在更好的相关性。我们对 108 个野生型和 52 个扩展型 ATXN3 等位基因的 gDNA 和 cDNA 样本进行了(CAG)(n)重复序列分析。在野生型等位基因中,gDNA 和 cDNA 之间没有差异。在扩展型等位基因中,gDNA 中的 CAG 重复序列并不总是直接转录到 mRNA 中;平均而言,cDNA 水平上有+1 个重复的差异。所得的微小差异不足以导致扩展等位基因分布的显著差异,因此,mRNA 并没有改善发病时间变异的解释。

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本文引用的文献

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Analysis of segregation patterns in Machado-Joseph disease pedigrees.马查多-约瑟夫病家系的分离模式分析。
J Hum Genet. 2008;53(10):920-923. doi: 10.1007/s10038-008-0330-y. Epub 2008 Aug 9.

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