Landgraf Pablo, Mayerhofer Peter U, Polanetz Roman, Roscher Adelbert A, Holzinger Andreas
Dr. von Hauner Children's Hospital, Department of Clinical Chemistry, Laboratory of Molecular Biology, Ludwig-Maximilians-University Munich, Munich, Germany.
Eur J Cell Biol. 2003 Aug;82(8):401-10. doi: 10.1078/0171-9335-00331.
In this study we addressed the targeting requirements of peroxisomal ABC transporters, in particular the human adrenoleukodystrophy protein. This membrane protein is defective or missing in X-linked adrenoleukodystrophy, a neurodegenerative disorder predominantly presenting in childhood. Using adrenoleukodystrophy protein deletion constructs and green fluorescent protein fusion constructs we identified the amino acid regions 1-110 and 67-164 to be sufficient for peroxisomal targeting. However, the minimal region shared by these constructs (amino acids 67-110) is not sufficient for peroxisomal targeting by itself. Additionally, the NH2-terminal 66 amino acids enhance targeting efficiency. Green fluorescent protein-labeled fragments of human peroxisomal membrane protein 69 and Saccharomyces cerevisiae Pxa1 corresponding to the amino acid 67-164 adrenoleukodystrophy protein region were also directed to the mammalian peroxisome. The required region contains a 14-amino-acid motif (71-84) conserved between the adrenoleukodystrophy protein and human peroxisomal membrane protein 69 and yeast Pxa1. Omission or truncation of this motif in the adrenoleukodystrophy protein abolished peroxisomal targeting. The single amino acid substitution L78F resulted in a significant reduction of targeting efficiency. The in-frame deletion of three amino acids (del78-80LLR) within the proposed targeting motif in two patients suffering from X-linked adrenoleukodystrophy resulted in the mislocalization of a green fluorescent protein fusion protein to nucleus, cytosol and mitochondria. Our data define the targeting region of human adrenoleukodystrophy protein containing a highly conserved 14-amino-acid motif.
在本研究中,我们探讨了过氧化物酶体ABC转运蛋白的靶向要求,特别是人类肾上腺脑白质营养不良蛋白。这种膜蛋白在X连锁肾上腺脑白质营养不良中存在缺陷或缺失,这是一种主要在儿童期出现的神经退行性疾病。我们使用肾上腺脑白质营养不良蛋白缺失构建体和绿色荧光蛋白融合构建体,确定氨基酸区域1 - 110和67 - 164足以实现过氧化物酶体靶向。然而,这些构建体共有的最小区域(氨基酸67 - 110)本身不足以实现过氧化物酶体靶向。此外,NH2末端的66个氨基酸可提高靶向效率。与肾上腺脑白质营养不良蛋白区域氨基酸67 - 164相对应的人类过氧化物酶体膜蛋白69和酿酒酵母Pxa1的绿色荧光蛋白标记片段也被导向哺乳动物过氧化物酶体。所需区域包含一个在肾上腺脑白质营养不良蛋白、人类过氧化物酶体膜蛋白69和酵母Pxa1之间保守的14个氨基酸基序(71 - 84)。在肾上腺脑白质营养不良蛋白中缺失或截断该基序会消除过氧化物酶体靶向。单个氨基酸取代L78F导致靶向效率显著降低。在两名患有X连锁肾上腺脑白质营养不良的患者中,在所提出的靶向基序内框内缺失三个氨基酸(del78 - 80LLR)导致绿色荧光蛋白融合蛋白错误定位于细胞核、细胞质和线粒体。我们的数据确定了人类肾上腺脑白质营养不良蛋白的靶向区域,该区域包含一个高度保守的14个氨基酸基序。