Multiple functions of mfa-1, a putative pheromone precursor gene of Neurospora crassa

Eukaryot Cell. 2002 Dec;1(6):987-99. doi: 10.1128/EC.1.6.987-999.2002.

Abstract

A putative pheromone precursor gene of Neurospora crassa, mfa-1 (which encodes mating factor a-1), was identified as the most abundant clone in starved mycelial and perithecial cDNA libraries. Northern analysis demonstrated high mfa-1 expression in all mating type a tissues and suggested low expression levels in mat A tissues. The mfa-1 gene was expressed as an approximately 1.2-kb transcript predicted to encode a 24-residue peptide, followed by a long 3' untranslated region (3' UTR). The predicted MFA1 sequence showed 100% sequence identity to PPG2 of Sordaria macrospora and structural similarity (a carboxy-terminal CAAX motif) to many hydrophobic fungal pheromone precursors. Mutants with a disrupted open reading frame (ORF) in which the critical cysteine residue had been changed to a nonprenylatable residue, tyrosine (YAAX mutants), were isolated, as were mfa-1 mutants with intact ORFs but multiple mutations in the 3' noncoding region (CAAX mutants). The 3' UTR is required for the full range of mfa-1 gene activity. Both classes of mutants showed delayed and reduced vegetative growth (which was suppressed by supplementation with a minute amount [30 micro M] of ornithine, citrulline, or arginine), as well as aberrant sexual development. When crossed as female parents to wild-type males, the CAAX and YAAX mutants showed greatly reduced ascospore production. No ascospores were produced in homozygous mfa-1 crosses. As males, YAAX mat a mutants were unable to attract wild-type mat A trichogynes (female-specific hyphae) or to initiate sexual development, while CAAX mat a mutants were able to mate and produce sexual progeny despite their inability to attract mat A trichogynes. In the mat A background, both CAAX and YAAX mutants showed normal male fertility but defective vegetative growth and aberrant female sexual development. Thus, the mfa-1 gene appears to have multiple roles in N. crassa development: (i) it encodes a hydrophobic pheromone with a putative farnesylated and carboxymethylated C-terminal cysteine residue, required by mat a to attract trichogynes of mat A; (ii) it is involved in female sexual development and ascospore production in both mating types; and (iii) it functions in vegetative growth of both mating types.

Publication types

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

MeSH terms

  • 3' Untranslated Regions
  • Base Sequence
  • Blotting, Southern
  • Cell Division
  • Chromosome Mapping
  • Crosses, Genetic
  • Cysteine / chemistry
  • DNA, Complementary / metabolism
  • Fungal Proteins / chemistry*
  • Fungal Proteins / metabolism
  • Gene Library
  • Genes, Fungal
  • Genes, Mating Type, Fungal
  • Genetic Complementation Test
  • Methylation
  • Molecular Sequence Data
  • Mutation
  • Neurospora crassa / genetics*
  • Neurospora crassa / physiology*
  • Nucleic Acid Conformation
  • Open Reading Frames
  • Pheromones / chemistry*
  • Pheromones / metabolism
  • Plasmids / metabolism
  • Point Mutation
  • Polymorphism, Restriction Fragment Length
  • Protein Prenylation
  • Protein Structure, Tertiary
  • Sequence Analysis, DNA
  • Sequence Homology, Nucleic Acid

Substances

  • 3' Untranslated Regions
  • DNA, Complementary
  • Fungal Proteins
  • Pheromones
  • Cysteine