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马查多-约瑟夫病(MJD)、齿状核红核苍白球路易体萎缩症(DRPLA)以及脊髓延髓肌萎缩症(SBMA)相关基因的信使核糖核酸(mRNA)中,三核苷酸重复序列CAG发生体细胞镶嵌现象。

Somatic mosaicism of the expanded CAG trinucleotide repeat in mRNAs for the responsible gene of Machado-Joseph disease (MJD), dentatorubral-pallidoluysian atrophy (DRPLA), and spinal and bulbar muscular atrophy (SBMA).

作者信息

Ito Y, Tanaka F, Yamamoto M, Doyu M, Nagamatsu M, Riku S, Mitsuma T, Sobue G

机构信息

Department of Neurology, Nagoya University, School of Medicine, Japan.

出版信息

Neurochem Res. 1998 Jan;23(1):25-32. doi: 10.1023/a:1022441101801.

Abstract

The CAG trinucleotide repeats in mRNAs for the responsible genes of Machado-Joseph disease (MJD), dentatorubral-pallidoluysian atrophy (DRPLA), and X-linked spinal and bulbal muscular atrophy (SBMA) were examined in various neural and nonneural tissues of affected individuals. The tissue-specific variation of expanded CAG repeat alleles were apparent for mRNAs of all three genes. The expanded CAG repeats of the mRNA were shorter in the cerebellum than in other regions of the central nervous system in DRPLA and MJD, but not in SBMA, and were longer in the liver and colon in MJD. Transcripts of the responsible genes with expanded CAG repeats were detected in all tissues studied, and the tissue-specific variation in the CAG repeat size of the mRNA did not correlate with the tissue-specific severity of pathological involvement in these diseases.

摘要

在患有马查多-约瑟夫病(MJD)、齿状核红核苍白球路易体萎缩症(DRPLA)和X连锁脊髓和延髓肌萎缩症(SBMA)的个体的各种神经组织和非神经组织中,检测了致病基因mRNA中的CAG三核苷酸重复序列。对于这三个基因的mRNA,扩增的CAG重复等位基因的组织特异性变异是明显的。在DRPLA和MJD中,mRNA的扩增CAG重复序列在小脑中比在中枢神经系统的其他区域短,但在SBMA中并非如此,而在MJD中,其在肝脏和结肠中更长。在所有研究的组织中均检测到具有扩增CAG重复序列的致病基因转录本,并且mRNA中CAG重复序列大小的组织特异性变异与这些疾病中病理累及的组织特异性严重程度无关。

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