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Unequal Recombination and Evolution of the Mating-Type (MAT) Loci in the Pathogenic Fungus Grosmannia clavigera and Relatives

Identifieur interne : 000959 ( Main/Exploration ); précédent : 000958; suivant : 000960

Unequal Recombination and Evolution of the Mating-Type (MAT) Loci in the Pathogenic Fungus Grosmannia clavigera and Relatives

Auteurs : Clement K.-M. Tsui [Canada] ; Scott Diguistini [Canada] ; Ye Wang [Canada] ; Nicolas Feau [Canada] ; Braham Dhillon [Canada] ; Jörg Bohlmann [Canada] ; Richard C. Hamelin [Canada]

Source :

RBID : PMC:3583454

Abstract

Sexual reproduction in fungi is regulated by the mating-type (MAT) locus where recombination is suppressed. We investigated the evolution of MAT loci in eight fungal species belonging to Grosmannia and Ophiostoma (Sordariomycetes, Ascomycota) that include conifer pathogens and beetle symbionts. The MAT1-2 idiomorph/allele was identified from the assembled and annotated Grosmannia clavigera genome, and the MAT locus is flanked by genes coding for cytoskeleton protein (SLA) and DNA lyase. The synteny of these genes is conserved and consistent with other members in Ascomycota. Using sequences from SLA and flanking regions, we characterized the MAT1-1 idiomorph from other isolates of G. clavigera and performed dotplot analysis between the two idiomorphs. Unexpectedly, the MAT1-2 idiomorph contains a truncated MAT1-1-1 gene upstream of the MAT1-2-1 gene that bears the high-mobility-group domain. The nucleotide and amino acid sequence of the truncated MAT1-1-1 gene is similar to its homologous copy in the MAT1-1 idiomorph in the opposite mating-type isolate, except that positive selection is acting on the truncated gene and the alpha(α)-box that encodes the transcription factor has been deleted. The MAT idiomorphs sharing identical gene organization were present in seven additional species in the Ophiostomatales, suggesting that the presence of truncated MAT1-1-1 gene is a general pattern in this order. We propose that an ancient unequal recombination event resulted in the ancestral MAT1-1-1 gene integrated into the MAT1-2 idiomorph and surviving as the truncated MAT1-1-1 genes. The α-box domain of MAT1-1-1 gene, located at the same MAT locus adjacent to the MAT1-2-1 gene, could have been removed by deletion after recombination due to mating signal interference. Our data confirmed a 1:1 MAT/sex ratio in two pathogen populations, and showed that all members of the Ophiostomatales studied here including those that were previously deemed asexual have the potential to reproduce sexually. This ability can potentially increase genetic variability and can enhance fitness in new, ecological niches.


Url:
DOI: 10.1534/g3.112.004986
PubMed: 23450093
PubMed Central: 3583454


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<p>Sexual reproduction in fungi is regulated by the mating-type (
<italic>MAT</italic>
) locus where recombination is suppressed. We investigated the evolution of
<italic>MAT</italic>
loci in eight fungal species belonging to
<italic>Grosmannia</italic>
and
<italic>Ophiostoma</italic>
(Sordariomycetes, Ascomycota) that include conifer pathogens and beetle symbionts. The
<italic>MAT1-2</italic>
idiomorph/allele was identified from the assembled and annotated
<italic>Grosmannia clavigera</italic>
genome, and the
<italic>MAT</italic>
locus is flanked by genes coding for cytoskeleton protein (
<italic>SLA</italic>
) and DNA lyase. The synteny of these genes is conserved and consistent with other members in Ascomycota. Using sequences from
<italic>SLA</italic>
and flanking regions, we characterized the
<italic>MAT1-1</italic>
idiomorph from other isolates of
<italic>G. clavigera</italic>
and performed dotplot analysis between the two idiomorphs. Unexpectedly, the
<italic>MAT1-2</italic>
idiomorph contains a truncated
<italic>MAT1-1-1</italic>
gene upstream of the
<italic>MAT1-2-1</italic>
gene that bears the high-mobility-group domain. The nucleotide and amino acid sequence of the truncated
<italic>MAT1-1-1</italic>
gene is similar to its homologous copy in the
<italic>MAT1-1</italic>
idiomorph in the opposite mating-type isolate, except that positive selection is acting on the truncated gene and the alpha(α)-box that encodes the transcription factor has been deleted. The
<italic>MAT</italic>
idiomorphs sharing identical gene organization were present in seven additional species in the Ophiostomatales, suggesting that the presence of truncated
<italic>MAT1-1-1</italic>
gene is a general pattern in this order. We propose that an ancient unequal recombination event resulted in the ancestral
<italic>MAT1-1-1</italic>
gene integrated into the
<italic>MAT1-2</italic>
idiomorph and surviving as the truncated
<italic>MAT1-1-1</italic>
genes. The α-box domain of
<italic>MAT1-1-1</italic>
gene, located at the same
<italic>MAT</italic>
locus adjacent to the
<italic>MAT1-2-1</italic>
gene, could have been removed by deletion after recombination due to mating signal interference. Our data confirmed a 1:1 MAT/sex ratio in two pathogen populations, and showed that all members of the Ophiostomatales studied here including those that were previously deemed asexual have the potential to reproduce sexually. This ability can potentially increase genetic variability and can enhance fitness in new, ecological niches.</p>
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<li>Colombie-Britannique </li>
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<li>Vancouver</li>
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