Involvement of Pex13p in Pex14p localization and peroxisomal targeting signal 2-dependent protein import into peroxisomes

被引:150
作者
Girzalsky, W
Rehling, P
Stein, K
Kipper, J
Blank, L
Kunau, WH
Erdmann, R
机构
[1] Free Univ Berlin, Inst Biochem, D-12203 Berlin, Germany
[2] Ruhr Univ Bochum, Inst Physiol Chem, D-44780 Bochum, Germany
关键词
peroxisome; peroxin; Pex13p; Pex14p; protein import;
D O I
10.1083/jcb.144.6.1151
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Pex13p is the putative docking protein for peroxisomal targeting signal 1 (PTS1)-dependent protein import into peroxisomes. Pex14p interacts with both the PTS1- and PTS2-receptor and may represent the paint of convergence of the PTS1- and PTS2-dependent protein import pathways. We report the involvement of Pex13p in peroxisomal import of PTS2-containing proteins. Like Pex14p, Pex13p not only interacts with the PTS1-receptor Pex5p, but also with the PTS2-receptor Pex7p; however, this association may be direct or indirect. In support of distinct peroxisomal binding sites for Pex7p, the Pex7p/Pex13p and Pex7p/Pex14p complexes can form independently. Genetic evidence for the interaction of Pex7p and Pex13p is provided by the observation that overexpression of Pex13p suppresses a loss of function mutant of Pex7p, Accordingly, we conclude that Pex7p and Pex13p functionally interact during PTS2-dependent protein import into peroxisomes. NH2-terminal regions of Pex13p are required for its interaction with the PTS2-receptor while the COOH-terminal SH3 domain alone is sufficient to mediate its interaction with the PTS1-receptor. Reinvestigation of the topology revealed both termini of Pex13p to be oriented towards the cytosol. We also found Pex13p to be required for peroxisomal association of Pex14p, yet the SH3 domain of Pex13p may not provide the only binding site for Pex14p at the peroxisomal membrane.
引用
收藏
页码:1151 / 1162
页数:12
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