ER-associated degradation in health and disease - from substrate to organism.

J Cell Sci

Department of Molecular & Integrative Physiology, University of Michigan Medical School, Ann Arbor, MI 48105, USA

Published: December 2019

AI Article Synopsis

  • The recent literature emphasizes the critical role of endoplasmic reticulum-associated degradation (ERAD) in maintaining health and combating disease.
  • The Sel1L-Hrd1 pathway is particularly important for normal bodily functions and protecting against various diseases, depending on the specific substrate and cell type involved.
  • This review focuses on three key aspects of ERAD: its two forms (constitutive vs. inducible), its role in regulating protein quality vs. quantity, and its influence on nuclear gene transcription, showcasing its overall impact on physiological processes.

Article Abstract

The recent literature has revolutionized our view on the vital importance of endoplasmic reticulum (ER)-associated degradation (ERAD) in health and disease. Suppressor/enhancer of Lin-12-like (Sel1L)-HMG-coA reductase degradation protein 1 (Hrd1)-mediated ERAD has emerged as a crucial determinant of normal physiology and as a sentinel against disease pathogenesis in the body, in a largely substrate- and cell type-specific manner. In this Review, we highlight three features of ERAD, constitutive versus inducible ERAD, quality versus quantity control of ERAD and ERAD-mediated regulation of nuclear gene transcription, through which ERAD exerts a profound impact on a number of physiological processes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6918741PMC
http://dx.doi.org/10.1242/jcs.232850DOI Listing

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