遗传学
基因座(遗传学)
错义突变
生物
基因
点突变
候选基因
天冬酰胺
异亮氨酸
突变
分子生物学
氨基酸
亮氨酸
作者
Ephrat Levy‐Lahad,Wilma Wasco,Parvoneh Poorkaj,Donna Romano,Junko Oshima,Warren H. Pettingell,Chang-En Yu,P. D. Jondro,Stephen D. Schmidt,Kai Wang,Annette C. Crowley,Ying‐Hui Fu,Suzanne Y. Guénette,David J. Galas,Ellen Nemens,Ellen M. Wijsman,Thomas D. Bird,Gerard D. Schellenberg,Rudolph E. Tanzi
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1995-08-18
卷期号:269 (5226): 973-977
被引量:2590
标识
DOI:10.1126/science.7638622
摘要
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.
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