Li X, Greenwald I
Integrated Program in Cellular, Molecular and Biophysical Studies, Columbia University College of Physicians and Surgeons, New York, NY 10032, USA.
Proc Natl Acad Sci U S A. 1998 Jun 9;95(12):7109-14. doi: 10.1073/pnas.95.12.7109.
Presenilins have been implicated in the genesis of Alzheimer's disease and in facilitating LIN-12/Notch activity during development. All presenilins have multiple hydrophobic regions that could theoretically span a membrane, and a description of the membrane topology is a crucial step toward deducing the mechanism of presenilin function. Previously, we proposed an eight-transmembrane-domain model for presenilin, based on studies of the Caenorhabditis elegans SEL-12 presenilin. Here, we describe experiments that support the view that two of the hydrophobic regions of SEL-12 function as the seventh and eighth transmembrane domains. Furthermore, we have shown that human presenilin 1 behaves like SEL-12 presenilin when analyzed by our methods. Our results provide additional experimental support for the eight-transmembrane-domain model of presenilin topology.
早老素与阿尔茨海默病的发病机制有关,并且在发育过程中促进LIN-12/Notch活性。所有早老素都有多个理论上可跨越膜的疏水区域,膜拓扑结构的描述是推断早老素功能机制的关键步骤。此前,基于对秀丽隐杆线虫SEL-12早老素的研究,我们提出了早老素的八跨膜结构域模型。在此,我们描述了一些实验,这些实验支持SEL-12的两个疏水区域作为第七和第八跨膜结构域的观点。此外,我们已经表明,当用我们的方法分析时,人早老素1的行为与SEL-12早老素相似。我们的结果为早老素拓扑结构的八跨膜结构域模型提供了额外的实验支持。