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Eukaryotic Cell, April 2005, p. 661-672, Vol. 4, No. 4
1535-9778/05/$08.00+0     doi:10.1128/EC.4.4.661-672.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Functional Characterization of an {alpha}-Factor-Like Sordaria macrospora Peptide Pheromone and Analysis of Its Interaction with Its Cognate Receptor in Saccharomyces cerevisiae

Severine Mayrhofer and Stefanie Pöggeler*

Lehrstuhl für Allgemeine und Molekulare Botanik, Ruhr-Universität, Bochum, Germany

Received 21 December 2004/ Accepted 12 February 2005

The homothallic filamentous ascomycete Sordaria macrospora possesses genes which are thought to encode two pheromone precursors and two seven-transmembrane pheromone receptors. The pheromone precursor genes are termed ppg1 and ppg2. The putative products derived from the gene sequence show structural similarity to the {alpha}-factor precursors and a-factor precursors of the yeast Saccharomyces cerevisiae. Likewise, sequence similarity has been found between the putative products of the pheromone receptor genes pre2 and pre1 and the S. cerevisiae Ste2p {alpha}-factor receptor and Ste3p a-factor receptor, respectively. To investigate whether the {alpha}-factor-like pheromone-receptor pair of S. macrospora is functional, a heterologous yeast assay was used. Our results show that the S. macrospora {alpha}-factor-like pheromone precursor PPG1 is processed into an active pheromone by yeast MAT{alpha} cells. The S. macrospora PRE2 protein was demonstrated to be a peptide pheromone receptor. In yeast MATa cells lacking the endogenous Ste2p receptor, the S. macrospora PRE2 receptor facilitated all aspects of the pheromone response. Using a synthetic peptide, we can now predict the sequence of one active form of the S. macrospora peptide pheromone. We proved that S. macrospora wild-type strains secrete an active pheromone into the culture medium and that disruption of the ppg1 gene in S. macrospora prevents pheromone production. However, loss of the ppg1 gene does not affect vegetative growth or fertility. Finally, we established the yeast assay as an easy and useful system for analyzing pheromone production in developmental mutants of S. macrospora.

* Corresponding author. Mailing address: Lehrstuhl für Allgemeine und Molekulare Botanik, Ruhr-Universität, 44780 Bochum, Germany. Phone: 49-234-3224264. Fax: 49-234-3214184. E-mail: Stefanie.Poeggeler{at}ruhr-uni-bochum.de.

Eukaryotic Cell, April 2005, p. 661-672, Vol. 4, No. 4
1535-9778/05/$08.00+0     doi:10.1128/EC.4.4.661-672.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.



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