Phytochelatin synthase genes from Arabidopsis and the yeast Schizosaccharomyces pombe

Plant Cell. 1999 Jun;11(6):1153-64. doi: 10.1105/tpc.11.6.1153.

Abstract

Phytochelatins (PCs), a family of heavy metal-inducible peptides important in the detoxification of heavy metals, have been identified in plants and some microorganisms, including Schizosaccharomyces pombe, but not in animals. PCs are synthesized enzymatically from glutathione (GSH) by PC synthase in the presence of heavy metal ions. In Arabidopsis, the CAD1 gene, identified by using Cd-sensitive, PC-deficient cad1 mutants, has been proposed to encode PC synthase. Using a positional cloning strategy, we have isolated the CAD1 gene. Database searches identified a homologous gene in S. pombe, and a mutant with a targeted deletion of this gene was also Cd sensitive and PC deficient. Extracts of Escherichia coli cells expressing a CAD1 cDNA or the S. pombe gene catalyzing GSH-dependent, heavy metal-activated synthesis of PCs in vitro demonstrated that both genes encode PC synthase activity. Both enzymes were activated by a range of metal ions. In contrast, reverse transcription-polymerase chain reaction experiments showed that expression of the CAD1 mRNA is not influenced by the presence of Cd. A comparison of the two predicted amino acid sequences revealed a highly conserved N-terminal region, which is presumed to be the catalytic domain, and a variable C-terminal region containing multiple Cys residues, which is proposed to be involved in activation of the enzyme by metal ions. Interestingly, a similar gene was identified in the nematode, Caenorhabditis elegans, suggesting that PCs may also be expressed in some animal species.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Aminoacyltransferases / chemistry
  • Aminoacyltransferases / genetics*
  • Aminoacyltransferases / metabolism
  • Arabidopsis / enzymology*
  • Arabidopsis / genetics*
  • Cloning, Molecular
  • Escherichia coli
  • Exons
  • Genes, Plant
  • Introns
  • Molecular Sequence Data
  • Polymorphism, Genetic
  • Polymorphism, Restriction Fragment Length
  • Recombinant Proteins / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Schizosaccharomyces / enzymology*
  • Schizosaccharomyces / genetics*
  • Sequence Alignment
  • Sequence Homology, Amino Acid

Substances

  • Recombinant Proteins
  • Aminoacyltransferases
  • glutathione gamma-glutamylcysteinyltransferase