| Literature DB >> 25605922 |
Chengcheng Huang1, Yoichiro Harada2, Akira Hosomi2, Yuki Masahara-Negishi2, Junichi Seino2, Haruhiko Fujihira2, Yoko Funakoshi2, Takehiro Suzuki3, Naoshi Dohmae3, Tadashi Suzuki4.
Abstract
The cytoplasmic peptide:N-glycanase (PNGase; Ngly1 in mice) is a deglycosylating enzyme involved in the endoplasmic reticulum (ER)-associated degradation (ERAD) process. The precise role of Ngly1 in the ERAD process, however, remains unclear in mammals. The findings reported herein, using mouse embryonic fibroblast (MEF) cells, that the ablation of Ngly1 causes dysregulation of the ERAD process. Interestingly, not only delayed degradation but also the deglycosylation of a misfolded glycoprotein was observed in Ngly1(-/-) MEF cells. The unconventional deglycosylation reaction was found to be catalyzed by the cytosolic endo-β-N-acetylglucosaminidase (ENGase), generating aggregation-prone N-GlcNAc proteins. The ERAD dysregulation in cells lacking Ngly1 was restored by the additional knockout of ENGase gene. Thus, our study underscores the functional importance of Ngly1 in the ERAD process and provides a potential mechanism underlying the phenotypic consequences of a newly emerging genetic disorder caused by mutation of the human NGLY1 gene.Entities:
Keywords: ENGase; ERAD; PNGase (Ngly1); glycoprotein; protein aggregates
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Year: 2015 PMID: 25605922 PMCID: PMC4321286 DOI: 10.1073/pnas.1414593112
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205