Ito Y, Tanaka F, Sobue G
Department of Neurology, Higashinagoya National Hospital.
Nihon Rinsho. 1999 Apr;57(4):850-5.
The somatic mosaicism of CAG repeat expansion in the neural tissues of a dentatorubral-pallidoluysian atrophy (DRPLA) was reviewed. The size of the major bands of the expanded allele was significantly smaller in the cerebellar cortex, however no significant difference was recognized in other regions of neuronal tissues. This showed that severity of neuropathological involvement in DRPLA is not parallel to the size of the expanded allele, indicating somatic mosaicism doesn't explain the selective neurodegeneration in DRPLA. The mechanism underlying the somatic mosaicism remains unknown. However, somatic CAG instability, cell division and some tissue specific factors may closely relate to the occurrence of the somatic mosaicism.
对齿状核红核苍白球路易体萎缩症(DRPLA)神经组织中CAG重复序列扩增的体细胞镶嵌现象进行了综述。在小脑皮质中,扩增等位基因的主要条带大小明显较小,然而在神经元组织的其他区域未发现显著差异。这表明DRPLA中神经病理受累的严重程度与扩增等位基因的大小不平行,提示体细胞镶嵌现象无法解释DRPLA中的选择性神经变性。体细胞镶嵌现象的潜在机制仍然未知。然而,体细胞CAG不稳定性、细胞分裂和一些组织特异性因素可能与体细胞镶嵌现象的发生密切相关。