The unknown face of IRE1α - Beyond ER stress

Eur J Cell Biol. 2018 Jun;97(5):359-368. doi: 10.1016/j.ejcb.2018.05.002. Epub 2018 May 4.

Abstract

IRE1α (Inositol Requiring kinase Enzyme 1 alpha), a transmembrane protein localized to the endoplasmic reticulum (ER) is a master regulator of the unfolded protein response (UPR) pathway. The fate determining steps during ER stress-induced apoptosis are greatly attributed to IRE1α's endoribonuclease and kinase activities. Apart from its role as a chief executioner in ER stress, recent studies have shown that upon activation in the presence or absence of ER stress, IRE1α executes multiple cellular processes such as differentiation, immune response, progression and repression of the cell cycle. Besides its crucial role in protein misfolding, the versatile contributions of IRE1α in other cellular functions are greatly unknown. In this review, we have discussed the structural conservation of IRE1 among eukaryotes, the mechanisms underlying its activation and the recent understandings of the non-apoptotic functions of IRE1 other than ER stress-induced cell death.

Keywords: Endoribonuclease; RIDD; UPR; XBP1.

Publication types

  • Review

MeSH terms

  • Endoplasmic Reticulum Stress / physiology*
  • Endoribonucleases / genetics*
  • Endoribonucleases / metabolism
  • Humans
  • Protein Serine-Threonine Kinases / genetics*
  • Protein Serine-Threonine Kinases / metabolism

Substances

  • ERN1 protein, human
  • Protein Serine-Threonine Kinases
  • Endoribonucleases