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来自人类大脑的具有长CAG三核苷酸重复序列的互补DNA。

cDNAs with long CAG trinucleotide repeats from human brain.

作者信息

Margolis R L, Abraham M R, Gatchell S B, Li S H, Kidwai A S, Breschel T S, Stine O C, Callahan C, McInnis M G, Ross C A

机构信息

Laboratory of Molecular Neurobiology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.

出版信息

Hum Genet. 1997 Jul;100(1):114-22. doi: 10.1007/s004390050476.

Abstract

Twelve diseases, most with neuropsychiatric features, arise from trinucleotide repeat expansion mutations. Expansion mutations may also cause a number of other disorders, including several additional forms of spinocerebellar ataxia, bipolar affective disorder, schizophrenia, and autism. To obtain candiate genes for these disorders, cDNA libraries from adult and fetal human brain were screened at high stringency for clones containing CAG repeats. Nineteen cDNAs were isolated and mapped to chromosomes 1, 2, 4, 6, 7, 8, 9, 12, 16, 19, 20, and X. The clones contain between 4 and 17 consecutive CAG, CTG, TCG, or GCA triplets. Clone H44 encodes 40 consecutive glutamines, more than any other entry in the nonredundant GenBank protein database and well within the range that causes neuronal degeneration in several of the glutamine expansion diseases. Eight cDNAs encode 15 or more consecutive glutamine residues, suggesting that the gene products may function as transcription factors, with a potential role in the regulation of neurodevelopment or neuroplasticity. In particular, the conceptual translation of clone CTG3a contains 18 consecutive glutamines and is 45% identical to the C-terminal 306 residues of the mouse numb gene product. These genes are therefore candidates for diseases featuring anticipation, neurodegeneration, or abnormalities of neurodevelopment.

摘要

12种疾病(大多数具有神经精神特征)由三核苷酸重复扩增突变引起。扩增突变还可能导致许多其他疾病,包括几种额外形式的脊髓小脑共济失调、双相情感障碍、精神分裂症和自闭症。为了获得这些疾病的候选基因,对来自成人和胎儿人脑的cDNA文库进行了高严格度筛选,以寻找含有CAG重复序列的克隆。分离出19个cDNA,并将其定位到1、2、4、6、7、8、9、12、16、19、20号染色体和X染色体上。这些克隆包含4至17个连续的CAG、CTG、TCG或GCA三联体。克隆H44编码40个连续的谷氨酰胺,比非冗余GenBank蛋白质数据库中的任何其他条目都多,且处于几种谷氨酰胺扩增疾病中导致神经元变性的范围内。8个cDNA编码15个或更多连续的谷氨酰胺残基,这表明基因产物可能作为转录因子发挥作用,在神经发育或神经可塑性的调节中具有潜在作用。特别是,克隆CTG3a的概念性翻译包含18个连续的谷氨酰胺,与小鼠麻木基因产物的C末端306个残基有45%的同一性。因此,这些基因是具有遗传早现、神经变性或神经发育异常特征疾病的候选基因。

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