期刊
JOURNAL OF BIOLOGICAL CHEMISTRY
卷 289, 期 20, 页码 14089-14108出版社
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M113.527937
关键词
Peroxisomes; Protein Targeting; Ubiquitin; Ubiquitin Ligase; Ubiquitination; Pex5p; RING Peroxins; Peroxisome Biogenesis
资金
- Global Centers of Excellence Program
- Ministry of Education, Culture, Sports, Science, and Technology of Japan
- SORST grant from the Science and Technology Agency of Japan
- CREST grant from the Science and Technology Agency of Japan
- Takeda Science Foundation
- Japanese Foundation for Applied Enzymology
- [19058011]
- [20370039]
- [24247038]
- [25112518]
- [1977087]
- [21770117]
- [24770130]
- Grants-in-Aid for Scientific Research [24770130, 25112518, 26116007, 25116717] Funding Source: KAKEN
Background: Pex5p translocates the cargo proteins into peroxisomes. Results: Mammalian RING peroxins, the Pex10pPex12p complex, catalyze Lys-linked, multiple monoubiquitination of Pex5p, assuring efficient export of Pex5p from peroxisomes. Conclusion: Distinct Lys- and Cys-linked modes of Pex5p ubiquitination control Pex5p-mediated matrix protein import. Significance: This work provides the first evidence of a functional role of mammalian RING peroxins in Pex5p ubiquitination. Peroxisome targeting signal type-1 (PTS1) receptor, Pex5p, is a key player in peroxisomal matrix protein import. Pex5p recognizes PTS1 cargoes in the cytosol, targets peroxisomes, translocates across the membrane, unloads the cargoes, and shuttles back to the cytosol. Ubiquitination of Pex5p at a conserved cysteine is required for the exit from peroxisomes. However, any potential ubiquitin ligase (E3) remains unidentified in mammals. Here, we establish an in vitro ubiquitination assay system and demonstrate that RING finger Pex10p functions as an E3 with an E2, UbcH5C. The E3 activity of Pex10p is essential for its peroxisome-restoring activity, being enhanced by another RING peroxin, Pex12p. The Pex10pPex12p complex catalyzes monoubiquitination of Pex5p at one of multiple lysine residues in vitro, following the dissociation of Pex5p from Pex14p and the PTS1 cargo. Several lines of evidence with lysine-to-arginine mutants of Pex5p demonstrate that Pex10p RING E3-mediated ubiquitination of Pex5p is required for its efficient export from peroxisomes to the cytosol and peroxisomal matrix protein import. RING peroxins are required for both modes of Pex5p ubiquitination, thus playing a pivotal role in Pex5p shuttling.
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