A cold-stress-inducible PERK/OGT axis controls TOM70-assisted mitochondrial protein import and cristae formation

Cell Metab. 2021 Mar 2;33(3):598-614.e7. doi: 10.1016/j.cmet.2021.01.013. Epub 2021 Feb 15.

Abstract

The architecture of cristae provides a spatial mitochondrial organization that contains functional respiratory complexes. Several protein components including OPA1 and MICOS complex subunits organize cristae structure, but upstream regulatory mechanisms are largely unknown. Here, in vivo and in vitro reconstitution experiments show that the endoplasmic reticulum (ER) kinase PERK promotes cristae formation by increasing TOM70-assisted mitochondrial import of MIC19, a critical subunit of the MICOS complex. Cold stress or β-adrenergic stimulation activates PERK that phosphorylates O-linked N-acetylglucosamine transferase (OGT). Phosphorylated OGT glycosylates TOM70 on Ser94, enhancing MIC19 protein import into mitochondria and promoting cristae formation and respiration. In addition, PERK-activated OGT O-GlcNAcylates and attenuates CK2α activity, which mediates TOM70 Ser94 phosphorylation and decreases MIC19 mitochondrial protein import. We have identified a cold-stress inter-organelle PERK-OGT-TOM70 axis that increases cell respiration through mitochondrial protein import and subsequent cristae formation. These studies have significant implications in cellular bioenergetics and adaptations to stress conditions.

Keywords: MIC19; PERK-OGT axis; TOM70; brown adipocytes; cold stress; cristae biogenesis; mitochondrial protein import; respiration.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes, Brown / cytology
  • Adipocytes, Brown / drug effects
  • Adipocytes, Brown / metabolism
  • Animals
  • Casein Kinase II / metabolism
  • Cold Temperature
  • Endoplasmic Reticulum / metabolism
  • Endoplasmic Reticulum Stress
  • GTP Phosphohydrolases / genetics
  • GTP Phosphohydrolases / metabolism
  • Glycosylation
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mitochondria / metabolism
  • Mitochondria / pathology
  • Mitochondrial Precursor Protein Import Complex Proteins / genetics
  • Mitochondrial Precursor Protein Import Complex Proteins / metabolism*
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / metabolism*
  • N-Acetylglucosaminyltransferases / genetics
  • N-Acetylglucosaminyltransferases / metabolism*
  • Phosphorylation
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Protein Transport
  • RNA, Guide, CRISPR-Cas Systems
  • eIF-2 Kinase / antagonists & inhibitors
  • eIF-2 Kinase / deficiency
  • eIF-2 Kinase / genetics
  • eIF-2 Kinase / metabolism*

Substances

  • Mitochondrial Precursor Protein Import Complex Proteins
  • Mitochondrial Proteins
  • Protein Isoforms
  • Tom70 protein, mouse
  • N-Acetylglucosaminyltransferases
  • Ogt protein, mouse
  • Casein Kinase II
  • PERK kinase
  • eIF-2 Kinase
  • GTP Phosphohydrolases
  • Opa1 protein, mouse