van der Klei I J, Hilbrands R E, Swaving G J, Waterham H R, Vrieling E G, Titorenko V I, Cregg J M, Harder W, Veenhuis M
Department of Microbiology, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Haren, The Netherlands.
J Biol Chem. 1995 Jul 21;270(29):17229-36. doi: 10.1074/jbc.270.29.17229.
PER genes are essential for the assembly of peroxisomes in Hansenula polymorpha. Here we describe the PER3 gene which was cloned by functional complementation of a H. polymorpha per3 mutant. The complementing PER3 gene encodes a protein of 569 amino acids (Per3p) with a calculated mass of 63.9 kDa; Per3p belongs to the tetratricopeptide repeat protein family and is located in both the cytosol and the peroxisomal matrix. Remarkably, Per3p does not contain a known targeting signal (PTS1 or PTS2). The PER3 gene product shows similarity to the Saccharomyces cerevisiae Pas10p (40% identity) and the Pichia pastoris Pas8p (55% identity). However, their function apparently cannot be interchanged since the P. pastoris PAS8 gene failed to functionally complement a H. polymorpha per3 disruption mutant. The per3 disruption mutant contained normal but small peroxisomes in which PTS2 proteins (both homologous and heterologous) were imported. Other matrix proteins (in particular PTS1 proteins) resided in the cytosol where they were normally assembled and active. We argue that Per3p is a component of the peroxisomal import machinery and most probably shuttles matrix proteins from the cytosol to the organellar matrix.
PER基因对于多形汉逊酵母中过氧化物酶体的组装至关重要。在此,我们描述了通过多形汉逊酵母per3突变体的功能互补克隆得到的PER3基因。互补的PER3基因编码一种含有569个氨基酸的蛋白质(Per3p),计算分子量为63.9 kDa;Per3p属于四肽重复蛋白家族,定位于细胞质溶胶和过氧化物酶体基质中。值得注意的是,Per3p不包含已知的靶向信号(PTS1或PTS2)。PER3基因产物与酿酒酵母的Pas10p(同一性为40%)和巴斯德毕赤酵母的Pas8p(同一性为55%)相似。然而,它们的功能显然不能互换,因为巴斯德毕赤酵母的PAS8基因不能在功能上互补多形汉逊酵母的per3缺失突变体。per3缺失突变体含有正常但较小的过氧化物酶体,其中PTS2蛋白(同源和异源)被导入。其他基质蛋白(特别是PTS1蛋白)存在于细胞质溶胶中,它们在那里正常组装并具有活性。我们认为Per3p是过氧化物酶体导入机制的一个组成部分,很可能将基质蛋白从细胞质溶胶转运到细胞器基质中。