Unidirectional mating-type switching is underpinned by a conserved MAT1 locus architecture

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dc.contributor.author Wilken, Pieter Markus
dc.contributor.author Lane, Frances Alice
dc.contributor.author Steenkamp, Emma Theodora
dc.contributor.author Wingfield, Michael J.
dc.contributor.author Wingfield, Brenda D.
dc.date.accessioned 2024-08-30T06:59:04Z
dc.date.available 2024-08-30T06:59:04Z
dc.date.issued 2024-02
dc.description.abstract Unidirectional mating-type switching is a form of homothallic reproduction known only in a small number of filamentous ascomycetes. Their ascospores can give rise to either self-sterile isolates that require compatible partners for subsequent sexual reproduction, or self-fertile individuals capable of completing this process in isolation. The limited studies previously conducted in these fungi suggest that the differences in mating specificity are determined by the architecture of the MAT1 locus. In self-fertile isolates that have not undergone unidirectional mating-type switching, the locus contains both MAT1-1 and MAT1-2 mating-type genes, typical of primary homothallism. In the self-sterile isolates produced after a switching event, the MAT1-2 genes are lacking from the locus, likely due to a recombination-mediated deletion of the MAT1-2 gene information. To determine whether these arrangements of the MAT1 locus support unidirectional mating-type switching in the Ceratocystidaceae, the largest known fungal assemblage capable of this reproduction strategy, a combination of genetic and genomic approaches were used. The MAT1 locus was annotated in representative species of Ceratocystis, Endoconidiophora, and Davidsoniella. In all cases, MAT1-2 genes interrupted the MAT1-1–1 gene in self-fertile isolates. The MAT1-2 genes were flanked by two copies of a direct repeat that accurately predicted the boundaries of the deletion event that would yield the MAT1 locus of self-sterile isolates. Although the relative position of the MAT1-2 gene region differed among species, it always disrupted the MAT1-1–1 gene and/or its expression in the self-fertile MAT1 locus. Following switching, this gene and/or its expression was restored in the self-sterile arrangement of the locus. This mirrors what has been reported in other species capable of unidirectional mating-type switching, providing the strongest support for a conserved MAT1 locus structure that is associated with this process. This study contributes to our understanding of the evolution of unidirectional mating-type switching. en_US
dc.description.department Biochemistry en_US
dc.description.department Forestry and Agricultural Biotechnology Institute (FABI) en_US
dc.description.department Genetics en_US
dc.description.department Microbiology and Plant Pathology en_US
dc.description.librarian hj2024 en_US
dc.description.sdg SDG-15:Life on land en_US
dc.description.sponsorship The Claude Leon Foundation and the University of Pretoria, the South African Department of Science and Technology (DST) and National Research Foundation (NRF) for funding via the Centres of Excellence programme (Centre of Excellence in Tree Heath Biotechnology) and the South African Research Chairs Initiative (SARChI; SARChI Chair in Fungal Genomics). en_US
dc.description.uri https://www.elsevier.com/locate/yfgbi en_US
dc.identifier.citation Wilken, P.M., Lane, F.A., Steenkamp, E.T. et al. 2024, 'Unidirectional mating-type switching is underpinned by a conserved MAT1 locus architecture', Fungal Genetics and Biology, vol. 170, art. 103859, pp. 1-10, doi : 10.1016/j.fgb.2023.103859. en_US
dc.identifier.issn 1087-1845
dc.identifier.other 10.1016/j.fgb.2023.103859
dc.identifier.uri http://hdl.handle.net/2263/97933
dc.language.iso en en_US
dc.publisher Elsevier en_US
dc.rights © 2023 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license. en_US
dc.subject Sexual reproduction en_US
dc.subject Ceratocystidaceae en_US
dc.subject Ceratocystis en_US
dc.subject Davidsoniella en_US
dc.subject Endoconidiophora en_US
dc.subject SDG-15: Life on land en_US
dc.title Unidirectional mating-type switching is underpinned by a conserved MAT1 locus architecture en_US
dc.type Article en_US


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