Regulation of physiological rates in Caenorhabditis elegans by a tRNA-modifying enzyme in the mitochondria

Genetics. 2001 Sep;159(1):147-57. doi: 10.1093/genetics/159.1.147.


We show that the phenotype associated with gro-1(e2400) comprises the whole suite of features that characterize the phenotype of the clk mutants in Caenorhabditis elegans, including deregulated developmental, behavioral, and reproductive rates, as well as increased life span and a maternal effect. We cloned gro-1 and found that it encodes a highly conserved cellular enzyme, isopentenylpyrophosphate:tRNA transferase (IPT), which modifies a subset of tRNAs. In yeast, two forms of the enzyme are produced by alternative translation initiation, one of which is mitochondrial. In the gro-1 transcript there are also two possible initiator ATGs, between which there is a sequence predicted to encode a mitochondrial localization signal. A functional GRO-1::GFP fusion protein is localized diffusely throughout the cytoplasm and nucleus. A GRO-1::GFP initiated from the first methionine is localized exclusively to the mitochondria and rescues the mutant phenotype. In contrast, a protein initiated from the second methionine is localized diffusely throughout the cell and does not rescue the mutant phenotype. As oxygen consumption and ATP concentration have been reported to be unaffected in gro-1 mutants, our observations suggest that GRO-1 acts in mitochondria and regulates global physiology by unknown mechanisms.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Alkyl and Aryl Transferases / chemistry*
  • Alkyl and Aryl Transferases / genetics*
  • Amino Acid Sequence
  • Animals
  • Caenorhabditis elegans / genetics*
  • Caenorhabditis elegans / metabolism*
  • Chromosome Mapping
  • Cloning, Molecular
  • Female
  • Green Fluorescent Proteins
  • Luminescent Proteins / metabolism
  • Male
  • Mitochondria / enzymology*
  • Models, Genetic
  • Molecular Sequence Data
  • Mutation
  • Operon
  • Oxygen Consumption
  • Phenotype
  • Polymerase Chain Reaction
  • Protein Binding
  • Protein Biosynthesis
  • RNA / metabolism
  • RNA Splicing
  • RNA, Messenger / metabolism
  • RNA, Transfer / metabolism*
  • Recombinant Fusion Proteins / metabolism
  • Sequence Homology, Amino Acid
  • Time Factors


  • Luminescent Proteins
  • RNA, Messenger
  • Recombinant Fusion Proteins
  • Green Fluorescent Proteins
  • RNA
  • Adenosine Triphosphate
  • RNA, Transfer
  • Alkyl and Aryl Transferases
  • tRNA isopentenyltransferase