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导致三联体重复疾病——齿状核红核苍白球路易体萎缩症(DRPLA)的基因的结构与表达

Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA).

作者信息

Nagafuchi S, Yanagisawa H, Ohsaki E, Shirayama T, Tadokoro K, Inoue T, Yamada M

机构信息

National Children's Medical Research Center, Tokyo, Japan.

出版信息

Nat Genet. 1994 Oct;8(2):177-82. doi: 10.1038/ng1094-177.

Abstract

Dentatorubral and pallidoluysian atrophy is associated with expansion of an unstable CAG repeat on chromosome 12p. We have determined the nucleotide sequences of overlapping cDNA clones and deduced the gene structure. The gene is ubiquitously expressed to form a single 4.5 kb transcript and encoded by an open reading frame of 1184 amino acids (aa), in which a polyglutamine track with variable length starts at aa 484. Although the predicted amino acid sequence does not reveal any function, it does contain several interesting motifs consisting of a simple repeated amino acid sequence, a homo-proline track, two stretches of arginine-glutamic acid dipeptides and a stretch of alternative histidine residues. These results provide clues toward understanding neurodegenerative diseases associated with triplet repeat expansion.

摘要

齿状红核苍白球萎缩症与12号染色体短臂上不稳定的CAG重复序列的扩增有关。我们已经确定了重叠cDNA克隆的核苷酸序列并推导了基因结构。该基因在全身广泛表达,形成一个单一的4.5kb转录本,由一个1184个氨基酸(aa)的开放阅读框编码,其中一个长度可变的聚谷氨酰胺序列从第484个氨基酸开始。虽然预测的氨基酸序列没有揭示任何功能,但它确实包含几个有趣的基序,由一个简单的重复氨基酸序列、一个同型脯氨酸序列、两段精氨酸-谷氨酸二肽和一段交替的组氨酸残基组成。这些结果为理解与三联体重复序列扩增相关的神经退行性疾病提供了线索。

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