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早发性家族性阿尔茨海默病中一个携带错义突变基因的克隆

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease.

作者信息

Sherrington R, Rogaev E I, Liang Y, Rogaeva E A, Levesque G, Ikeda M, Chi H, Lin C, Li G, Holman K, Tsuda T, Mar L, Foncin J F, Bruni A C, Montesi M P, Sorbi S, Rainero I, Pinessi L, Nee L, Chumakov I, Pollen D, Brookes A, Sanseau P, Polinsky R J, Wasco W, Da Silva H A, Haines J L, Perkicak-Vance M A, Tanzi R E, Roses A D, Fraser P E, Rommens J M, St George-Hyslop P H

机构信息

Department of Medicine (Neurology), University of Toronto, Ontario, Canada.

出版信息

Nature. 1995 Jun 29;375(6534):754-60. doi: 10.1038/375754a0.

Abstract

Some cases of Alzheimer's disease are inherited as an autosomal dominant trait. Genetic linkage studies have mapped a locus (AD3) associated with susceptibility to a very aggressive form of Alzheimer's disease to chromosome 14q24.3. We have defined a minimal cosegregating region containing the AD3 gene, and isolated at least 19 different transcripts encoded within this region. One of these transcripts (S182) corresponds to a novel gene whose product is predicted to contain multiple transmembrane domains and resembles an integral membrane protein. Five different missense mutations have been found that cosegregate with early-onset familial Alzheimer's disease. Because these changes occurred in conserved domains of this gene, and are not present in normal controls, they are likely to be causative of AD3.

摘要

某些阿尔茨海默病病例以常染色体显性性状遗传。基因连锁研究已将与一种极具侵袭性的阿尔茨海默病易感性相关的一个基因座(AD3)定位到14号染色体的q24.3区域。我们已经确定了一个包含AD3基因的最小共分离区域,并分离出了该区域内编码的至少19种不同转录本。其中一种转录本(S182)对应一个新基因,其产物预计含有多个跨膜结构域,类似于一种整合膜蛋白。已发现五个不同的错义突变与早发性家族性阿尔茨海默病共分离。由于这些变化发生在该基因的保守结构域中,且在正常对照中不存在,它们很可能是AD3的病因。

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