Dodt G, Braverman N, Wong C, Moser A, Moser H W, Watkins P, Valle D, Gould S J
Kennedy Krieger Research Institute, Department of Cell Biology and Anatomy, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.
Nat Genet. 1995 Feb;9(2):115-25. doi: 10.1038/ng0295-115.
The peroxisome biogenesis disorders (PBDs) are lethal recessive diseases caused by defects in peroxisome assembly. We have isolated PXR1, a human homologue of the yeast P. pastoris PAS8 (peroxisome assembly) gene. PXR1, like PAS8, encodes a receptor for proteins with the type-1 peroxisomal targeting signal (PTS1). Mutations in PXR1 define complementation group 2 of PBDs and expression of PXR1 rescues the PTS1 import defect of fibroblasts from these patients. Based on the observation that PXR1 exists both in the cytosol and in association with peroxisomes, we propose that PXR1 protein recognizes PTS1-containing proteins in the cytosol and directs them to the peroxisome.
过氧化物酶体生物发生障碍(PBDs)是由过氧化物酶体组装缺陷引起的致死性隐性疾病。我们分离出了PXR1,它是酵母巴斯德毕赤酵母PAS8(过氧化物酶体组装)基因的人类同源物。与PAS8一样,PXR1编码一种针对具有1型过氧化物酶体靶向信号(PTS1)的蛋白质的受体。PXR1中的突变定义了PBDs的互补组2,并且PXR1的表达挽救了这些患者成纤维细胞的PTS1导入缺陷。基于PXR1既存在于细胞质中又与过氧化物酶体相关联的观察结果,我们提出PXR1蛋白在细胞质中识别含PTS1的蛋白质并将它们导向过氧化物酶体。