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1号染色体家族性阿尔茨海默病位点的候选基因。

Candidate gene for the chromosome 1 familial Alzheimer's disease locus.

作者信息

Levy-Lahad E, Wasco W, Poorkaj P, Romano D M, Oshima J, Pettingell W H, Yu C E, Jondro P D, Schmidt S D, Wang K

机构信息

Geriatric Research Education, and Clinical Center (182B), Veterans Affairs Medical Center, Seattle, WA 98108, USA.

出版信息

Science. 1995 Aug 18;269(5226):973-7. doi: 10.1126/science.7638622.

Abstract

A candidate gene for the chromosome 1 Alzheimer's disease (AD) locus was identified (STM2). The predicted amino acid sequence for STM2 is homologous to that of the recently cloned chromosome 14 AD gene (S182). A point mutation in STM2, resulting in the substitution of an isoleucine for an asparagine (N141l), was identified in affected people from Volga German AD kindreds. This N141l mutation occurs at an amino acid residue that is conserved in human S182 and in the mouse S182 homolog. The presence of missense mutations in AD subjects in two highly similar genes strongly supports the hypothesis that mutations in both are pathogenic.

摘要

一个位于1号染色体上的阿尔茨海默病(AD)基因座的候选基因被鉴定出来(STM2)。STM2的预测氨基酸序列与最近克隆的14号染色体AD基因(S182)的序列同源。在来自伏尔加德意志AD家族的患病个体中,发现了STM2中的一个点突变,该突变导致异亮氨酸取代天冬酰胺(N141I)。这种N141I突变发生在一个在人类S182和小鼠S182同源物中保守的氨基酸残基处。两个高度相似的基因在AD受试者中都存在错义突变,这有力地支持了这两个基因中的突变都是致病性的这一假说。

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