Will G K, Soukupova M, Hong X, Erdmann K S, Kiel J A, Dodt G, Kunau W H, Erdmann R
Institut für Physiologische Chemie, Ruhr-Universität Bochum, 44780 Bochum, Germany.
Mol Cell Biol. 1999 Mar;19(3):2265-77. doi: 10.1128/MCB.19.3.2265.
Pex14p is a central component of the peroxisomal protein import machinery, which has been suggested to provide the point of convergence for PTS1- and PTS2-dependent protein import in yeast cells. Here we describe the identification of a human peroxisome-associated protein (HsPex14p) which shows significant similarity to the yeast Pex14p. HsPex14p is a carbonate-resistant peroxisomal membrane protein with its C terminus exposed to the cytosol. The N terminus of the protein is not accessible to exogenously added antibodies or protease and thus might protrude into the peroxisomal lumen. HsPex14p overexpression leads to the decoration of tubular structures and mislocalization of peroxisomal catalase to the cytosol. HsPex14p binds the cytosolic receptor for the peroxisomal targeting signal 1 (PTS1), a result consistent with a function as a membrane receptor in peroxisomal protein import. Homo-oligomerization of HsPex14p or interaction of the protein with the PTS2-receptor or HsPex13p was not observed. This distinguishes the human Pex14p from its counterpart in yeast cells and thus supports recent data suggesting that not all aspects of peroxisomal protein import are conserved between yeasts and humans. The role of HsPex14p in mammalian peroxisome biogenesis makes HsPEX14 a candidate PBD gene for being responsible for an unrecognized complementation group of human peroxisome biogenesis disorders.
Pex14p是过氧化物酶体蛋白导入机制的核心组成部分,有人认为它为酵母细胞中依赖PTS1和PTS2的蛋白导入提供了汇聚点。在此,我们描述了一种人类过氧化物酶体相关蛋白(HsPex14p)的鉴定,它与酵母Pex14p具有显著的相似性。HsPex14p是一种耐碳酸盐的过氧化物酶体膜蛋白,其C末端暴露于胞质溶胶。该蛋白的N末端对外源添加的抗体或蛋白酶不可接近,因此可能伸入过氧化物酶体腔。HsPex14p的过表达导致管状结构的修饰以及过氧化物酶体过氧化氢酶错误定位于胞质溶胶。HsPex14p结合过氧化物酶体靶向信号PTS1的胞质受体,这一结果与它作为过氧化物酶体蛋白导入中的膜受体的功能一致。未观察到HsPex14p的同源寡聚化或该蛋白与PTS2受体或HsPex13p的相互作用。这将人类Pex14p与其在酵母细胞中的对应物区分开来,因此支持了最近的数据,表明过氧化物酶体蛋白导入的并非所有方面在酵母和人类之间都是保守的。HsPex14p在哺乳动物过氧化物酶体生物发生中的作用使HsPEX14成为一个候选的PBD基因,可能与一组未被认识的人类过氧化物酶体生物发生障碍互补群有关。