Physiological importance of NGLY1, as revealed by rodent model analyses
- PMID: 34580715
- DOI: 10.1093/jb/mvab101
Physiological importance of NGLY1, as revealed by rodent model analyses
Erratum in
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Erratum.J Biochem. 2022 Mar 31;171(4):469. doi: 10.1093/jb/mvac016. J Biochem. 2022. PMID: 35181785 Free PMC article. No abstract available.
Abstract
Cytosolic peptide:N-glycanase (NGLY1) is an enzyme that cleaves N-glycans from glycoproteins that has been retrotranslocated from the endoplasmic reticulum (ER) lumen into the cytosol. It is known that NGLY1 is involved in the degradation of cytosolic glycans (non-lysosomal glycan degradation) as well as ER-associated degradation, a quality control system for newly synthesized glycoproteins. The discovery of NGLY1 deficiency, which is caused by mutations in the human NGLY1 gene and results in multisystemic symptoms, has attracted interest in the physiological functions of NGLY1 in mammals. Studies using various animal models led to the identification of possible factors that contribute to the pathogenesis of NGLY1 deficiency. In this review, we summarize phenotypic consequences that have been reported for various Ngly1-deficient rodent models and discuss future perspectives to provide more insights into the physiological functions of NGLY1.
Keywords: ENGASE; FBS2; NGLY1; NGLY1 deficiency; rodent model.
© The Author(s) 2021. Published by Oxford University Press on behalf of the Japanese Biochemical Society. All rights reserved.
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