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

J Cell Sci. 2019 Dec 2;132(23):jcs232850. doi: 10.1242/jcs.232850.

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.

Keywords: Constitutive ERAD; Disease; ERAD substrate, Quality control; Health; Inducible ERAD; Nuclear gene transcription; Quantity control; Sel1L-Hrd1 ERAD.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Endoplasmic Reticulum-Associated Degradation / genetics
  • Endoplasmic Reticulum-Associated Degradation / physiology*
  • Humans
  • Models, Biological
  • Proteins / genetics
  • Proteins / metabolism
  • Ubiquitin-Protein Ligases / genetics
  • Ubiquitin-Protein Ligases / metabolism

Substances

  • Proteins
  • SEL1L protein, human
  • SYVN1 protein, human
  • Ubiquitin-Protein Ligases