| Title: | Identification and functional analysis of pheromone and receptor genes in the B3 mating locus of Pleurotus eryngii |
| Author(s): | Kim KH; Kang YM; Im CH; Ali A; Kim SY; Je HJ; Kim MK; Rho HS; Lee HS; Kong WS; Ryu JS; |
| Address: | "Environment-friendly Research Division, Gyeongsangnam-do Agricultural Research and Extension Services, Jinju, Republic of Korea. Environment-friendly Research Division, Gyeongsangnam-do Agricultural Research and Extension Services, Jinju, Republic of Korea; Herbal Medicine Research Division, Korea Institute of Oriental Medicine (KIOM), Daejeon, Republic of Korea. Department of Microbiology, Gyeongsang National University, Jinju, Republic of Korea. Mushroom Research Division, National Institute of Horticultural and Herbal Science, Rural Development Administration, Eumsung, Republic of Korea" |
| DOI: | 10.1371/journal.pone.0104693 |
| ISSN/ISBN: | 1932-6203 (Electronic) 1932-6203 (Linking) |
| Abstract: | "Pleurotus eryngii has recently become a major cultivated mushroom; it uses tetrapolar heterothallism as a part of its reproductive process. Sexual development progresses only when the A and B mating types are compatible. Such mating incompatibility occasionally limits the efficiency of breeding programs in which crossing within loci-shared strains or backcrossing strategies are employed. Therefore, understanding the mating system in edible mushroom fungi will help provide a short cut in the development of new strains. We isolated and identified pheromone and receptor genes in the B3 locus of P. eryngii and performed a functional analysis of the genes in the mating process by transformation. A genomic DNA library was constructed to map the entire mating-type locus. The B3 locus was found to contain four pheromone precursor genes and four receptor genes. Remarkably, receptor PESTE3.3.1 has just 34 amino acid residues in its C-terminal cytoplasmic region; therefore, it seems likely to be a receptor-like gene. Real-time quantitative RT-PCR (real-time qRT-PCR) revealed that most pheromone and receptor genes showed significantly higher expression in monokaryotic cells than dikaryotic cells. The pheromone genes PEphb3.1 and PEphb3.3 and the receptor gene PESTE3.3.1 were transformed into P5 (A3B4). The transformants were mated with a tester strain (A4B4), and the progeny showed clamp connections and a normal fruiting body, which indicates the proposed role of these genes in mating and fruiting processes. This result also confirms that PESTE3.3.1 is a receptor gene. In this study, we identified pheromone and receptor genes in the B3 locus of P. eryngii and found that some of those genes appear to play a role in the mating and fruiting processes. These results might help elucidate the mechanism of fruiting differentiation and improve breeding efficiency" |
| Keywords: | "Amino Acid Sequence Fruiting Bodies, Fungal/genetics/metabolism Fungal Proteins/chemistry/*genetics/metabolism Gene Expression Genes, Fungal *Genes, Mating Type, Fungal Genetic Loci Molecular Sequence Data Pheromones/chemistry/*genetics/metabolism Pleurot;" |
| Notes: | "MedlineKim, Kyung-Hee Kang, Young Min Im, Chak Han Ali, Asjad Kim, Sun Young Je, Hee-Jeong Kim, Min-Keun Rho, Hyun Su Lee, Hyun Sook Kong, Won-Sik Ryu, Jae-San eng Research Support, Non-U.S. Gov't 2014/08/19 PLoS One. 2014 Aug 18; 9(8):e104693. doi: 10.1371/journal.pone.0104693. eCollection 2014" |
