Yamazaki H, Bujo H, Kusunoki J, Seimiya K, Kanaki T, Morisaki N, Schneider W J, Saito Y
Second Department of Internal Medicine, Chiba University School of Medicine, Chiba 260, Japan.
J Biol Chem. 1996 Oct 4;271(40):24761-8. doi: 10.1074/jbc.271.40.24761.
Normal cell development depends to a large part on multifunctional proteins that have evolved by recombination of proven modular elements. We now have discovered and characterized in rabbit such a multi-domain protein, and classify it as novel member of the low density lipoprotein (LDL) receptor gene family. The extracellular portion of the approximately 250-kDa membrane protein, termed LR11, contains a cluster of 11 LDL receptor ligand binding repeats, a group of 5 LDL receptor "YWTD" repeats, a large hexarepeat domain of structural elements found in neural cell adhesion molecules, and a domain with similarity to a yeast receptor for vacuolar protein sorting, VPS10. The cytoplasmic domain exhibits features typical of endocytosis-competent coated-pit receptors. The mosaic, and presumably multifunctional, receptor is expressed abundantly in brain, in particular the hippocampus, dentate gyrus, and cerebral cortex, and is present at significant levels in liver, adrenal glands, and testis. Western blotting of tissues and ligand blotting of LR11-transfected cells demonstrated that the novel protein binds apolipoprotein E-containing lipoproteins. In contrast to the LDL receptor, hepatic expression of LR11 is unaffected by hyperlipidemia. The identification of this highly conserved and superbly complex protein offers the opportunity to gain new insights into the emergence of multifunctional mosaic proteins akin to the ever expanding LDL receptor gene family.
正常细胞发育在很大程度上依赖于通过已证实的模块化元件重组而进化的多功能蛋白质。我们现在已经在兔子体内发现并鉴定了这样一种多结构域蛋白,并将其归类为低密度脂蛋白(LDL)受体基因家族的新成员。这种约250 kDa的膜蛋白的细胞外部分称为LR11,它包含一簇11个LDL受体配体结合重复序列、一组5个LDL受体“YWTD”重复序列、一个在神经细胞粘附分子中发现的由结构元件组成的大六重复结构域,以及一个与酵母液泡蛋白分选受体VPS10相似的结构域。细胞质结构域表现出具有内吞功能的被膜小窝受体的典型特征。这种镶嵌式且可能具有多功能的受体在脑中大量表达,特别是在海马体、齿状回和大脑皮层,并且在肝脏、肾上腺和睾丸中也有显著水平的表达。对组织进行蛋白质免疫印迹分析以及对LR11转染细胞进行配体印迹分析表明,这种新蛋白能结合含载脂蛋白E的脂蛋白。与LDL受体不同,LR11在肝脏中的表达不受高脂血症的影响。这种高度保守且极其复杂蛋白的鉴定为深入了解类似于不断扩展的LDL受体基因家族的多功能镶嵌蛋白的出现提供了机会。