Physiological importance of NGLY1, as revealed by rodent model analyses

Author:

Fujihira Haruhiko12,Asahina Makoto3,Suzuki Tadashi13

Affiliation:

1. Glycometabolic Biochemistry Laboratory, RIKEN Cluster for Pioneering Research, RIKEN, Saitama, 3510198, Japan

2. Division of Glycobiologics, Intractable Disease Research Center, Juntendo University Graduate School of Medicine, Tokyo, 1138421, Japan

3. T-CiRA Discovery, Takeda Pharmaceutical Company Ltd, Kanagawa, 2518555, Japan

Abstract

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.

Funder

Kyoto University

Japan Agency for Medical Research and Development-Core Research for Evolutional Science and Technology

RIKEN Pioneering Research Project

Grants-in-Aid for Scientific Research

Publisher

Oxford University Press (OUP)

Subject

Molecular Biology,Biochemistry,General Medicine

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