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早老素与阿尔茨海默病。

The presenilins and Alzheimer's disease.

作者信息

Hutton M, Hardy J

机构信息

Neurogenetics Laboratory, The Mayo Clinic Jacksonville, FL 32224, USA.

出版信息

Hum Mol Genet. 1997;6(10):1639-46. doi: 10.1093/hmg/6.10.1639.

Abstract

The presenilin 1 and presenilin 2 genes have been identified as pathogenic loci involved in the majority of early onset, autosomal dominant Alzheimer's disease. A series of (predominantly) missense mutations have been identified in the two genes which lead to disease. The presenilins are probably eight transmembrane domain proteins with both termini in the cytoplasmic compartment. They have a wide tissue distribution and are found in the endoplasmic reticulum and early Golgi. The mechanism of pathogenesis of the mutations is not clear although, both in patients and in in vitro systems, the effects of presenilin mutations are reminiscent of the effects of the pathogenic mutations in the amyloid precursor protein gene which lead to increases in the amount of amyloid-beta42(43) being produced from the metabolism of the amyloid protein precursor. Thus, the presenilin data provide independent support for the amyloid cascade hypothesis of Alzheimer's pathogenesis. Work on the Caenorhabditis elegans homologues of the presenilins, spe-4 and sel-12, suggests that the presenilins may have a more general and direct role in the processing and trafficking of membrane-bound proteins and that, in part, the pathogenic mutations may disrupt this role.

摘要

早老素1和早老素2基因已被确定为大多数早发性常染色体显性阿尔茨海默病的致病位点。在这两个导致疾病的基因中已鉴定出一系列(主要是)错义突变。早老素可能是具有八个跨膜结构域的蛋白质,其两端都位于细胞质区室。它们具有广泛的组织分布,存在于内质网和早期高尔基体中。尽管在患者和体外系统中,早老素突变的影响让人联想到淀粉样前体蛋白基因中的致病突变的影响,即导致淀粉样蛋白前体代谢产生的β淀粉样蛋白42(43)量增加,但突变的发病机制尚不清楚。因此,早老素的数据为阿尔茨海默病发病机制的淀粉样蛋白级联假说提供了独立支持。对早老素在秀丽隐杆线虫中的同源物spe-4和sel-12的研究表明,早老素可能在膜结合蛋白的加工和运输中具有更普遍和直接的作用,并且部分致病突变可能会破坏这一作用。

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