The clp1 Gene of the Mushroom Coprinus cinereus Is Essential for A-Regulated Sexual Development

• Published in: Genetics (Austin) Vol. 157; no. 1; pp. 133 - 140
• Main Authors: Inada, Kazumi, Morimoto, Yoshinori, Arima, Toshihide, Murata, Yukio, Kamada, Takashi
• Format: Journal Article
• Language: English
• Published: United States Genetics Soc America 01.01.2001; Genetics Society of America
• Subjects: Amino Acid Sequence; Base Sequence; Coprinus - genetics; Coprinus - growth & development; Deoxyribonucleic acid; DNA; DNA Primers - genetics; DNA, Fungal - genetics; Fungal Proteins - genetics; Gene Expression Regulation, Developmental; Genes; Genes, Fungal; Genes, Mating Type, Fungal; Molecular Sequence Data; Mushrooms; Mutation; Plant reproduction; Proteins
• ISSN: 0016-6731; 1943-2631; 1943-2631
• DOI: 10.1093/genetics/157.1.133

Sexual development in the mushroom Coprinus cinereus is under the control of the A and B mating-type loci, both of which must be different for a compatible, dikaryotic mycelium to form between two parents. The A genes, encoding proteins with homeodomain motifs, regulate conjugate division of the two nuclei from each mating partner and promote the formation of clamp connections. The latter are hyphal configurations required for the maintenance of the nuclear status in the dikaryotic phase of basidiomycetes. The B genes encode pheromones and pheromone receptors. They regulate the cellular fusions that complete clamp connections during growth, as well as the nuclear migration required for dikaryosis. The AmutBmut strain (326) of C. cinereus, in which both A- and B-regulated pathways are constitutively activated by mutations, produces, without mating, dikaryon-like, fertile hyphae with clamp connections. In this study we isolated and characterized clampless1-1 (clp1-1), a mutation that blocks clamp formation, an essential step in A-regulated sexual development, in the AmutBmut background. A genomic DNA fragment that rescues the clp1-1 mutation was identified by transformations. Sequencing of the genomic DNA, together with RACE experiments, identified an ORF interrupted by one intron, encoding a novel protein of 365 amino acids. The clp1-1 mutant allele carries a deletion of four nucleotides, which is predicted to cause elimination of codon 128 and frameshifts thereafter. The clp1 transcript was normally detected only in the presence of the A protein heterodimer formed when homokaryons with compatible A genes were mated. Forced expression of clp1 by promoter replacements induced clamp development without the need for a compatible A gene combination. These results indicate that expression of clp1 is necessary and sufficient for induction of the A-regulated pathway that leads to clamp development.