Saito Shinya, Araki Wataru
Department of Demyelinating Disease and Aging, National Institute of Neuroscience, NCNP, Kodaira, Tokyo 187-8502, Japan.
Biochem Biophys Res Commun. 2005 Feb 4;327(1):18-22. doi: 10.1016/j.bbrc.2004.11.130.
APH-1 is a polytopic membrane protein that functions as a component of presenilin-gamma-secretase complexes. Two homologous genes of APH-1 exist in humans, APH-1a and APH-1b, and alternative splicing of the former generates two isoforms, APH-1aS and APH-1aL. We performed semi-quantitative reverse transcription-PCR analysis to investigate mRNA expression of these three APH-1 forms in human cell lines and tissues. We found that both APH-1a and APH-1b were expressed in almost all tissues, and that APH-1aS was 1.5-3 times more abundantly expressed than APH-1aL. We examined the effect of small interfering RNA-mediated knock down of APH-1a or APH-1b on APH-1 mRNA expression and presenilin complex protein expression. We found that knock down of APH-1a, but not APH-1b, resulted in impaired maturation of nicastrin and reduced expression of presenilin 1, presenilin 2, and PEN-2 proteins. These findings indicate that APH-1a plays an essential role in the formation of presenilin-gamma-secretase complexes.
APH-1是一种多拓扑膜蛋白,作为早老素-γ-分泌酶复合物的一个组成部分发挥作用。人类中存在APH-1的两个同源基因,即APH-1a和APH-1b,前者的可变剪接产生两种异构体,APH-1aS和APH-1aL。我们进行了半定量逆转录聚合酶链反应分析,以研究这三种APH-1形式在人类细胞系和组织中的mRNA表达。我们发现APH-1a和APH-1b在几乎所有组织中均有表达,且APH-1aS的表达量比APH-1aL丰富1.5至3倍。我们研究了小干扰RNA介导的APH-1a或APH-1b敲低对APH-1 mRNA表达和早老素复合蛋白表达的影响。我们发现,APH-1a的敲低而非APH-1b的敲低,导致尼卡斯特林成熟受损以及早老素1、早老素2和PEN-2蛋白表达降低。这些发现表明,APH-1a在早老素-γ-分泌酶复合物的形成中起关键作用。