Tanaka F, Ito Y, Sobue G
Department of Neurology, Nagoya University School of Medicine.
Nihon Rinsho. 1999 Apr;57(4):862-8.
The CAG repeat in spinal and bulbar muscular atrophy (SBMA) is relatively stable in mitotic and meiotic processes as compared with other CAG repeat diseases. Previous reports indicate that SBMA does not manifest somatic mosaicism. However, detailed analysis in various tissues from 20 SBMA including 4 autopsied patients revealed the presence of the tissue-specific pattern of mosaicism. The prominent somatic mosaicism was observed in the cardiac and skeletal muscles, which are predominantly composed of postmitotic cells, and in the skin, prostate, and testis. The central nervous system (CNS) tissues, liver, and spleen showed smallest mosaicism. Such tissue-specific pattern of somatic mosaicism in SBMA is not explained by cell composition with different cell turnover rates. Other cell specific factors are likely more important for the somatic mosaicism in SBMA.
与其他CAG重复序列疾病相比,脊髓延髓肌肉萎缩症(SBMA)中的CAG重复序列在有丝分裂和减数分裂过程中相对稳定。先前的报告表明,SBMA不会表现出体细胞镶嵌现象。然而,对20例SBMA患者(包括4例尸检患者)的各种组织进行的详细分析显示,存在组织特异性的镶嵌模式。在主要由有丝分裂后细胞组成的心肌和骨骼肌以及皮肤、前列腺和睾丸中观察到明显的体细胞镶嵌现象。中枢神经系统(CNS)组织、肝脏和脾脏的镶嵌现象最少。SBMA中这种组织特异性的体细胞镶嵌模式不能用具有不同细胞更新率的细胞组成来解释。其他细胞特异性因素可能对SBMA中的体细胞镶嵌现象更为重要。