High diversity and complex evolution of fungal cytochrome P450 reductase: cytochrome P450 systems

Fungal Genet Biol. 2008 Apr;45(4):446-58. doi: 10.1016/j.fgb.2007.10.004. Epub 2007 Oct 15.

Abstract

Cytochrome P450 reductase (CPR) is the redox partner of P450 monooxygenases, involved in primary and secondary metabolism of eukaryotes. Two novel CPR genes, sharing 34% amino acid identity, were found in the filamentous ascomycete Cochliobolus lunatus. Fungal genomes were searched for putative CPR enzymes. Phylogenetic analysis suggests that multiple independent CPR duplication events occurred in fungi, whereas P450-CPR fusion occurred before the diversification of Dikarya and Zygomycota. Additionally, losses of methionine synthase reductase were found in certain fungal taxa; a truncated form of this enzyme was conserved in Pezizomycotina. In fungi, high numbers of cytochrome P450 enzymes, multiple CPRs, and P450-CPR fusion proteins were associated with filamentous growth. Evolution of multiple CPR-like oxidoreductases in filamentous fungi might have been driven by the complexity of biochemical functions necessitated by their growth form, as opposed to yeast.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ascomycota / enzymology*
  • Ascomycota / genetics
  • Cytochrome P-450 Enzyme System / genetics*
  • DNA, Fungal / chemistry
  • DNA, Fungal / genetics
  • Evolution, Molecular*
  • Ferredoxin-NADP Reductase / genetics
  • Fungal Proteins / genetics*
  • Gene Deletion
  • Gene Duplication
  • Gene Fusion
  • Genetic Variation*
  • Molecular Sequence Data
  • NADPH-Ferrihemoprotein Reductase / genetics*
  • Phylogeny
  • Sequence Analysis, DNA
  • Sequence Homology, Amino Acid

Substances

  • DNA, Fungal
  • Fungal Proteins
  • Cytochrome P-450 Enzyme System
  • methionine synthase reductase
  • Ferredoxin-NADP Reductase
  • NADPH-Ferrihemoprotein Reductase

Associated data

  • GENBANK/EU111680
  • GENBANK/EU111681