The yeast protein Ubx4p contributes to mitochondrial respiration and lithium-galactose-mediated activation of the unfolded protein response

J Biol Chem. 2020 Mar 20;295(12):3773-3782. doi: 10.1074/jbc.RA119.011271. Epub 2020 Jan 29.

Abstract

In the presence of galactose, lithium ions activate the unfolded protein response (UPR) by inhibiting phosphoglucomutase activity and causing the accumulation of galactose-related metabolites, including galactose-1-phosphate. These metabolites also accumulate in humans who have the disease classic galactosemia. Here, we demonstrate that Saccharomyces cerevisiae yeast strains harboring a deletion of UBX4, a gene encoding a partner of Cdc48p in the endoplasmic reticulum-associated degradation (ERAD) pathway, exhibit delayed UPR activation after lithium and galactose exposure because the deletion decreases galactose-1-phosphate levels. The delay in UPR activation did not occur in yeast strains in which key ERAD or proteasomal pathway genes had been disrupted, indicating that the ubx4Δ phenotype is ERAD-independent. We also observed that the ubx4Δ strain displays decreased oxygen consumption. The inhibition of mitochondrial respiration was sufficient to diminish galactose-1-phosphate levels and, consequently, affects UPR activation. Finally, we show that the deletion of the AMP-activated protein kinase ortholog-encoding gene SNF1 can restore the oxygen consumption rate in ubx4Δ strain, thereby reestablishing galactose metabolism, UPR activation, and cellular adaption to lithium-galactose challenge. Our results indicate a role for Ubx4p in yeast mitochondrial function and highlight that mitochondrial and endoplasmic reticulum functions are intertwined through galactose metabolism. These findings also shed new light on the mechanisms of lithium action and on the pathophysiology of galactosemia.

Keywords: ASPS-1; ASPSCR1; Caenorhabditis elegans (C. elegans); Saccharomyces cerevisiae; endoplasmic reticulum stress (ER stress); endoplasmic reticulum–associated protein degradation (ERAD); galactose; galactosemia; lithium; mitochondria.

Publication types

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

MeSH terms

  • Basic-Leucine Zipper Transcription Factors / genetics
  • Basic-Leucine Zipper Transcription Factors / metabolism
  • Endoplasmic Reticulum / metabolism
  • Galactose / metabolism
  • Galactose / pharmacology*
  • Galactosephosphates / metabolism
  • Intracellular Signaling Peptides and Proteins / deficiency
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Lithium / pharmacology*
  • Mitochondria / metabolism*
  • Oxygen Consumption
  • Protein Serine-Threonine Kinases / deficiency
  • Protein Serine-Threonine Kinases / genetics
  • RNA Splicing
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism
  • Saccharomyces cerevisiae / metabolism*
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / metabolism*
  • Unfolded Protein Response / drug effects*

Substances

  • Basic-Leucine Zipper Transcription Factors
  • Galactosephosphates
  • HAC1 protein, S cerevisiae
  • Intracellular Signaling Peptides and Proteins
  • Repressor Proteins
  • Saccharomyces cerevisiae Proteins
  • UBX4 protein, S cerevisiae
  • galactose-1-phosphate
  • Lithium
  • SNF1-related protein kinases
  • Protein Serine-Threonine Kinases
  • Galactose