Abstract
The a mating type locus of Ustilago maydis contains the structural genes for a pheromone-based cell recognition system that governs fusion of haploid cells. Binding of pheromone to its cognate receptor includes mating competence in haploid cells and stimulates filamentous growth of the dikaryon. We have analyzed transcription of genes located in the a locus and demonstrate that all genes are induced by pheromone. Transcriptional stimulation is mediated by a 9 bp DNA element (ACAAAGGGA) that occurs in multiple copies in both alleles of the a locus. By fusing multimers containing this 9 bp sequence to the pheromone gene promoter and to a heterologous promoter we demonstrate that this sequence acts as a pheromone response element. In addition, we show that expression of the b genes, which regulate pathogenic development of the dikaryon, is also stimulated by pheromone. Pheromone-inducible genes can be divided into three classes depending on whether their expression is reduced, maintained, or increased after cell fusion. These differences may suggest some regulatory cross-talk between the a and b loci.
MeSH Terms
Alleles
Base Sequence
DNA, Fungal/chemistry,metabolism
Gene Expression Regulation, Fungal
Genes, Fungal
Glucuronidase/biosynthesis
Haploidy
Mating Factor
Molecular Sequence Data
Peptide Biosynthesis
Peptides/genetics,physiology
Pheromones/physiology
Recombinant Proteins/biosynthesis
Regulatory Sequences, Nucleic Acid
Transcription, Genetic
Ustilago/genetics,physiology
Chemicals
DNA, Fungal
Peptides
Pheromones
Recombinant Proteins
Mating Factor
Glucuronidase
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Urban M
Institut für Genetik and Mikrobiologie, Universität München, Germany.
Kahmann R
Bölker M
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