Compromised Mitochondrial Protein Import Acts as a Signal for UPRmt

Cell Rep. 2019 Aug 13;28(7):1659-1669.e5. doi: 10.1016/j.celrep.2019.07.049.

Abstract

The induction of the mitochondrial unfolded protein response (UPRmt) results in increased transcription of the gene encoding the mitochondrial chaperone HSP70. We systematically screened the C. elegans genome and identified 171 genes that, when knocked down, induce the expression of an hsp-6 HSP70 reporter and encode mitochondrial proteins. These genes represent many, but not all, mitochondrial processes (e.g., mitochondrial calcium homeostasis and mitophagy are not represented). Knockdown of these genes leads to reduced mitochondrial membrane potential and, hence, decreased protein import into mitochondria. In addition, it induces UPRmt in a manner that is dependent on ATFS-1 but that is not antagonized by the kinase GCN-2. We propose that compromised mitochondrial protein import signals the induction of UPRmt and that the mitochondrial targeting sequence of ATFS-1 functions as a sensor for this signal.

Keywords: ATFS-1; C. elegans; GCN-2; UPR(mt); hsp-6; hsp-60; mitochondria.

Publication types

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

MeSH terms

  • Animals
  • Caenorhabditis elegans / genetics
  • Caenorhabditis elegans / growth & development
  • Caenorhabditis elegans / metabolism*
  • Caenorhabditis elegans Proteins / genetics
  • Caenorhabditis elegans Proteins / metabolism*
  • Calcium / metabolism*
  • Membrane Potential, Mitochondrial
  • Mitochondria / metabolism*
  • Mitochondria / pathology
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / metabolism*
  • Protein Kinases / genetics
  • Protein Kinases / metabolism*
  • Protein Transport
  • Stress, Physiological
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Unfolded Protein Response*

Substances

  • ATFS-1 protein, C elegans
  • Caenorhabditis elegans Proteins
  • Mitochondrial Proteins
  • Transcription Factors
  • Protein Kinases
  • gcn-2 protein, C elegans
  • Calcium