Functional characterization of the copper transcription factor AfMac1 from Aspergillus fumigatus

Biochem J. 2017 Jul 3;474(14):2365-2378. doi: 10.1042/BCJ20170191.

Abstract

Although copper functions as a cofactor in many physiological processes, copper overload leads to harmful effects in living cells. Thus, copper homeostasis is tightly regulated. However, detailed copper metabolic pathways have not yet been identified in filamentous fungi. In this report, we investigated the copper transcription factor AfMac1 ( Aspergillus fumigatusMac1 homolog) and identified its regulatory mechanism in A. fumigatus AfMac1 has domains homologous to the DNA-binding and copper-binding domains of Mac1 from Saccharomyces cerevisiae, and AfMac1 efficiently complemented Mac1 in S. cerevisiae Expression of Afmac1 resulted in CTR1 up-regulation, and mutation of the DNA-binding domain of Afmac1 failed to activate CTR1 expression in S. cerevisiae The Afmac1 deletion strain of A. fumigatus failed to grow in copper-limited media, and its growth was restored by introducing ctrC We found that AfMac1 specifically bound to the promoter region of ctrC based on EMSA. The AfMac1-binding motif 5'-TGTGCTCA-3' was identified from the promoter region of ctrC, and the addition of mutant ctrC lacking the AfMac1-binding motif failed to up-regulate ctrC in A. fumigatus Furthermore, deletion of Afmac1 significantly reduced strain virulence and activated conidial killing activity by neutrophils and macrophages. Taken together, these results suggest that AfMac1 is a copper transcription factor that regulates cellular copper homeostasis in A. fumigatus.

Keywords: A. fumigatus; Mac1; MrpA; S. cerevisiae; copper; iron.

MeSH terms

  • Amino Acid Substitution
  • Aspergillus fumigatus / enzymology
  • Aspergillus fumigatus / metabolism*
  • Aspergillus fumigatus / pathogenicity
  • Cation Transport Proteins / genetics
  • Cation Transport Proteins / metabolism
  • Chymotrypsin / chemistry
  • Chymotrypsin / genetics
  • Chymotrypsin / metabolism
  • Copper / metabolism*
  • Copper Transporter 1
  • Fungal Proteins / chemistry
  • Fungal Proteins / genetics
  • Fungal Proteins / metabolism*
  • Gene Deletion
  • Gene Expression Regulation, Fungal
  • Homeostasis
  • Laccase / metabolism*
  • Point Mutation
  • Promoter Regions, Genetic
  • Protein Interaction Domains and Motifs
  • Protein Transport
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / metabolism
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / metabolism
  • Sequence Alignment
  • Sequence Homology, Amino Acid
  • Superoxide Dismutase / metabolism*
  • Transcription Factors / chemistry
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Virulence
  • Virulence Factors / chemistry
  • Virulence Factors / genetics
  • Virulence Factors / metabolism*

Substances

  • CTR1 protein, S cerevisiae
  • Cation Transport Proteins
  • Copper Transporter 1
  • Fungal Proteins
  • Recombinant Proteins
  • Saccharomyces cerevisiae Proteins
  • Transcription Factors
  • Virulence Factors
  • Copper
  • Laccase
  • Superoxide Dismutase
  • Chymotrypsin
  • chymotrypsin C