Identification of an a-factor-like pheromone secreted by the heterothallic ascomycete Aspergillus fumigatus

Members of the fungal kingdom serve as models for numerous cellular processes, among them sexuality.<sup>1</sup> In heterothallic ascomycetes, mating-type systems ensure that only compatible isolates fuse to enter the sexual phase.<sup>2</sup><sup>,</sup><sup>3</sup><sup>,</sup><sup>4</sup><sup>,</sup><sup>5</sup><sup>,</sup><sup>6</sup> This includes reciprocal secretion and recognition of pheromones, commonly termed α-factor and a-factor, which are processed from peptide precursors.<sup>7</sup><sup>,</sup><sup>8</sup><sup>,</sup><sup>9</sup><sup>,</sup><sup>10</sup> Identification of fungal mating pheromones and their cognate receptors has been achieved by homology searches<sup>11</sup><sup>,</sup><sup>12</sup><sup>,</sup><sup>13</sup><sup>,</sup><sup>14</sup><sup>,</sup><sup>15</sup><sup>,</sup><sup>16</sup><sup>,</sup><sup>17</sup>; however, this approach had failed to detect a-factor-like pheromones from Eurotiomycetes,<sup>5</sup><sup>,</sup><sup>18</sup><sup>,</sup><sup>19</sup><sup>,</sup><sup>20</sup><sup>,</sup><sup>21</sup> a fungal group including medically and economically important species.<sup>22</sup> Sexuality of the opportunistic pathogen Aspergillus fumigatus<sup>23</sup><sup>,</sup><sup>24</sup><sup>,</sup><sup>25</sup> is genetically determined by a bipolar mating-type system encoding MAT1-1-1 and MAT1-2-1 regulators.<sup>16</sup><sup>,</sup><sup>26</sup><sup>,</sup><sup>27</sup><sup>,</sup><sup>28</sup><sup>,</sup><sup>29</sup><sup>,</sup><sup>30</sup> By analyzing transcriptome data from strains overexpressing the corresponding MAT genes,<sup>31</sup> we identified a candidate pheromone precursor gene B (ppgB) to encode the elusive Eurotiomycete a-factor pheromone. Its deduced peptide is 24 aa in length and features a canonical CaaX farnesylation motif. Further analyses provided supporting evidence that PpgB is a prototype for the a-factor-like pheromone of the aspergilli, including expression of ppgB in a MAT1-2-1-dependent manner, and that an A. fumigatus ppgBΔ deletion strain was unable to mate and form fruiting bodies with a compatible partner. Inspection of Aspergillus genomes from members of the section Fumigati revealed high conservation of PpgB sequence as well as of the α-factor-like PpgA, indicating that incompatibility factors other than solely pheromone discrimination are responsible for speciation. The identification of the A. fumigatusa-factor-like pheromone closes a substantial knowledge gap with respect to cellular recognition and sexual propagation of Eurotiomycete fungi.

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Journal
Current Biology
Published
2025-04-21
DOI
https://doi.org/10.1016/j.cub.2025.03.080
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1
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Fungal and yeast genetics research
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article
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article

Identification of an a-factor-like pheromone secreted by the heterothallic ascomycete Aspergillus fumigatus

Scott Baker, Stefanie Pöggeler, Tobias Pazen, Sven Krappmann et al.
1 citations
Current Biology
Fungal and yeast genetics research
0.81
article

Identification of an a-factor-like pheromone secreted by the heterothallic ascomycete Aspergillus fumigatus

Scott Baker, Stefanie Pöggeler, Tobias Pazen, Sven Krappmann, Yidong Yu, Olaf Kniemeyer, Minou Nowrousian, Paul S. Dyer, Jürgen Einsiedel, Peter Gmeiner, Thomas Krüger, Elisabeth Gabl, Anna Heizmann
article en
1 citations

Abstract

Members of the fungal kingdom serve as models for numerous cellular processes, among them sexuality.<sup>1</sup> In heterothallic ascomycetes, mating-type systems ensure that only compatible isolates fuse to enter the sexual phase.<sup>2</sup><sup>,</sup><sup>3</sup><sup>,</sup><sup>4</sup><sup>,</sup><sup>5</sup><sup>,</sup><sup>6</sup> This includes reciprocal secretion and recognition of pheromones, commonly termed α-factor and a-factor, which are processed from peptide precursors.<sup>7</sup><sup>,</sup><sup>8</sup><sup>,</sup><sup>9</sup><sup>,</sup><sup>10</sup> Identification of fungal mating pheromones and their cognate receptors has been achieved by homology searches<sup>11</sup><sup>,</sup><sup>12</sup><sup>,</sup><sup>13</sup><sup>,</sup><sup>14</sup><sup>,</sup><sup>15</sup><sup>,</sup><sup>16</sup><sup>,</sup><sup>17</sup>; however, this approach had failed to detect a-factor-like pheromones from Eurotiomycetes,<sup>5</sup><sup>,</sup><sup>18</sup><sup>,</sup><sup>19</sup><sup>,</sup><sup>20</sup><sup>,</sup><sup>21</sup> a fungal group including medically and economically important species.<sup>22</sup> Sexuality of the opportunistic pathogen Aspergillus fumigatus<sup>23</sup><sup>,</sup><sup>24</sup><sup>,</sup><sup>25</sup> is genetically determined by a bipolar mating-type system encoding MAT1-1-1 and MAT1-2-1 regulators.<sup>16</sup><sup>,</sup><sup>26</sup><sup>,</sup><sup>27</sup><sup>,</sup><sup>28</sup><sup>,</sup><sup>29</sup><sup>,</sup><sup>30</sup> By analyzing transcriptome data from strains overexpressing the corresponding MAT genes,<sup>31</sup> we identified a candidate pheromone precursor gene B (ppgB) to encode the elusive Eurotiomycete a-factor pheromone. Its deduced peptide is 24 aa in length and features a canonical CaaX farnesylation motif. Further analyses provided supporting evidence that PpgB is a prototype for the a-factor-like pheromone of the aspergilli, including expression of ppgB in a MAT1-2-1-dependent manner, and that an A. fumigatus ppgBΔ deletion strain was unable to mate and form fruiting bodies with a compatible partner. Inspection of Aspergillus genomes from members of the section Fumigati revealed high conservation of PpgB sequence as well as of the α-factor-like PpgA, indicating that incompatibility factors other than solely pheromone discrimination are responsible for speciation. The identification of the A. fumigatusa-factor-like pheromone closes a substantial knowledge gap with respect to cellular recognition and sexual propagation of Eurotiomycete fungi.

Current BiologyVol. 35(10)
University of Nottingham (GB), Friedrich-Alexander-Universität Erlangen-Nürnberg (DE), University Hospitals of the Ruhr-University of Bochum (DE), Environmental Molecular Sciences Laboratory (US), Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e. V. - Hans-Knöll-Institut (HKI) (DE), University of Göttingen (DE), Teikyo University (JP), Ruhr University Bochum (DE)
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Fungal and yeast genetics research
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