Mitochondrial dysfunction confers resistance to multiple drugs in Caenorhabditis elegans

Mol Biol Cell. 2010 Mar 15;21(6):956-69. doi: 10.1091/mbc.e09-08-0673. Epub 2010 Jan 20.

Abstract

In a previous genetic screen for Caenorhabditis elegans mutants that survive in the presence of an antimitotic drug, hemiasterlin, we identified eight strong mutants. Two of these were found to be resistant to multiple toxins, and in one of these we identified a missense mutation in phb-2, which encodes the mitochondrial protein prohibitin 2. Here we identify two additional mutations that confer drug resistance, spg-7 and har-1, also in genes encoding mitochondrial proteins. Other mitochondrial mutants, isp-1, eat-3, and clk-1, were also found to be drug-resistant. Respiratory complex inhibitors, FCCP and oligomycin, and a producer of reactive oxygen species (ROS), paraquat, all rescued wild-type worms from hemiasterlin toxicity. Worms lacking mitochondrial superoxide dismutase (MnSOD) were modestly drug-resistant, and elimination of MnSOD in the phb-2, har-1, and spg-7 mutants enhanced resistance. The antioxidant N-acetyl-l-cysteine prevented mitochondrial inhibitors from rescuing wild-type worms from hemiasterlin and sensitized mutants to the toxin, suggesting that a mechanism sensitive to ROS is necessary to trigger drug resistance in C. elegans. Using genetics, we show that this drug resistance requires pkc-1, the C. elegans ortholog of human PKCepsilon.

Publication types

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

MeSH terms

  • Adenylate Kinase / metabolism
  • Amino Acid Sequence
  • Animals
  • Caenorhabditis elegans / cytology*
  • Caenorhabditis elegans / drug effects
  • Caenorhabditis elegans / genetics
  • Caenorhabditis elegans / metabolism*
  • Caenorhabditis elegans Proteins / genetics
  • Caenorhabditis elegans Proteins / metabolism
  • Drug Resistance / physiology*
  • HeLa Cells
  • Herbicides / pharmacology
  • Humans
  • Methacrylates / pharmacology
  • Mitochondria / drug effects
  • Mitochondria / genetics
  • Mitochondria / metabolism*
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / metabolism
  • Molecular Sequence Data
  • Mutation
  • Oligopeptides / chemistry
  • Oligopeptides / pharmacology
  • Paraquat / pharmacology
  • Prohibitins
  • Protein Kinase C / metabolism
  • RNA Interference
  • Reactive Oxygen Species / metabolism
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism
  • Sequence Alignment
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase / metabolism
  • Thiazoles / pharmacology
  • Tubulin Modulators / pharmacology

Substances

  • Caenorhabditis elegans Proteins
  • HTI-286
  • Har-1 protein, C elegans
  • Herbicides
  • Methacrylates
  • Mitochondrial Proteins
  • Oligopeptides
  • PHB protein, human
  • PHB2 protein, human
  • Prohibitins
  • Reactive Oxygen Species
  • Repressor Proteins
  • Thiazoles
  • Tubulin Modulators
  • prohibitin 2, C elegans
  • hemiasterlin
  • myxothiazol
  • Superoxide Dismutase
  • Protein Kinase C
  • Adenylate Kinase
  • Paraquat