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A Deviation from the Bipolar-Tetrapolar Mating Paradigm in an Early Diverged Basidiomycete

  • Marco A. Coelho,

    Affiliation Centro de Recursos Microbiológicos (CREM), Departamento de Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, Caparica, Portugal

  • José Paulo Sampaio,

    Affiliation Centro de Recursos Microbiológicos (CREM), Departamento de Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, Caparica, Portugal

  • Paula Gonçalves

    Affiliation Centro de Recursos Microbiológicos (CREM), Departamento de Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, Caparica, Portugal

A Deviation from the Bipolar-Tetrapolar Mating Paradigm in an Early Diverged Basidiomycete

  • Marco A. Coelho, 
  • José Paulo Sampaio, 
  • Paula Gonçalves


In fungi, sexual identity is determined by specialized genomic regions called MAT loci which are the equivalent to sex chromosomes in some animals and plants. Usually, only two sexes or mating types exist, which are determined by two alternate sets of genes (or alleles) at the MAT locus (bipolar system). However, in the phylum Basidiomycota, a unique tetrapolar system emerged in which four different mating types are generated per meiosis. This occurs because two functionally distinct molecular recognition systems, each encoded by one MAT region, constrain the selection of sexual partners. Heterozygosity at both MAT regions is a pre-requisite for mating in both bipolar and tetrapolar basidiomycetes. Tetrapolar mating behaviour results from the absence of genetic linkage between the two regions bringing forth up to thousands of mating types. The subphylum Pucciniomycotina, an early diverged lineage of basidiomycetes encompassing important plant pathogens such as the rusts and saprobes like Rhodosporidium and Sporidiobolus, has been so far poorly explored concerning the content and organization of MAT loci. Here we show that the red yeast Sporidiobolus salmonicolor has a mating system unlike any previously described because occasional disruptions of the genetic cohesion of the bipolar MAT locus originate new mating types. We confirmed that mating is normally bipolar and that heterozygosity at both MAT regions is required for mating. However, a laboratory cross showed that meiotic recombination may occur within the bipolar MAT locus, explaining tetrapolar features like increased allele number and evolution rates of some MAT genes. This pseudo-bipolar system deviates from the classical bipolar–tetrapolar paradigm and, to our knowledge, has never been observed before. We propose a model for MAT evolution in the Basidiomycota in which the pseudo-bipolar system may represent a hitherto unforeseen gradual form of transition from an ancestral tetrapolar system to bipolarity.

Author Summary

Sexual reproduction in fungi is regulated by genomic regions called MAT loci that determine sexual identity in a manner comparable to that of sex chromosomes in animal and plants. In most fungi, sexual reproduction is bipolar, i.e., two alternate and distinct sets of genes at the MAT locus determine two mating types (the equivalent to sexes). In the Basidiomycota, which is the fungal lineage that includes the mushrooms, a unique (tetrapolar) sexual reproduction system evolved in which the mating type is determined by two functionally independent and genetically unlinked regions. In addition, the tetrapolar system functions with multiple alleles for at least one the two classes of MAT genes. This potentially generates thousands of mating types, as observed for many mushroom species. Here we report on the molecular characterization of the mating system in the basidiomycetous red yeast Sporidiobolus salmonicolor, which belongs to the Pucciniomycotina, the earliest derived lineage of the Basidiomycota that has remained virtually unexplored with respect to gene content and structure of MAT loci. Our results revealed for the first time a mating system that is neither tetrapolar nor strictly bipolar, and we propose a model for the evolution of basidiomycete MAT loci that accommodates this novel finding.


In fungi, sexual reproduction systems have been well characterized at the molecular level in numerous species belonging to the Ascomycota and the Basidiomycota, revealing striking similarities with sex determining regions in animals and plants [1] along with unique features such as the occurrence of thousands of sexual identity (mating) types in a single species [2]. Most fungi capable of sexual reproduction are heterothallic [3] which means that mating occurs only between distinct haploid individuals with compatible mating types. However, homothallic (self-fertile) mating is not unusual and several different genetic mechanisms have been shown to form the basis for this sexual behaviour [4][7].

Sexual reproduction systems in fungi have served as invaluable eukaryotic models of development [8], transcriptional regulation [9], [10] and signalling pathways [11] but research in the field has also been spurred by the fact that for many plant or animal pathogens, sexual reproduction is intimately linked with virulence (e.g. the human pathogens Cryptococcus neoformans and Candida albicans [12] or the maize smut Ustilago maydis [13]).

The chromosomal regions that determine the mating type in fungi are called the MAT loci and vary extensively in length and in genetic content in different fungal lineages. In most species within the Ascomycota, the two MAT loci in sexually compatible haploid individuals are short and contain completely unrelated sequences (idiomorphs) encoding transcription factors that regulate post-mating sexual development. These transcription factors belong to the alpha-domain, homeodomain or HMG families [14]. In the phylum Basidiomycota, mating of compatible haploid partners – homokaryotic hyphae or haploid yeast cells – originates a dikaryotic filamentous stage where subsequently basidia and basidiospores (meiospores) are formed [15]. Pioneering work on the mushroom Schizophyllum commune provided the first glimpse of a unique sexual compatibility system, the so-called tetrapolar or bifactorial system [16]. This system is only found in basidiomycetes because, unlike all other fungi studied so far, they possess two independent molecular determinants of mating type [17]. Sexual compatibility is usually determined at a first level by lipopetide pheromones and plasma membrane pheromone receptors that mediate cell-cell recognition, with the exception of some homobasidiomycetes (the lineage that includes the mushrooms) where fusion of homokaryotic hyphae is not restrained by pheromone-mediated interactions [2], [18]. After cell fusion, progression through the sexual cycle requires overcoming a second compatibility hurdle that relies on a heterodimeric homeodomain transcription factor (HD1/HD2), encoded by a pair of divergently transcribed, closely linked genes [3], [19][21]. The HD1/HD2 heterodimer is a transcriptional regulator of post-mating sexual development that is only active in the dikaryon because dimerization is restricted to subunits that originate from genetically different individuals. Dimerization of HD1 and HD2 proteins encoded by the same gene pair is prevented in haploid individuals by a self/non-self recognition mechanism that has been well characterized in mushrooms [22][24] and in smut fungi [25], [26]. These studies showed that the self/non-self recognition domain resides on the highly variable N-terminal portion of the proteins. Accordingly, in HD1 proteins of the mushroom Coprinus cinereus, this domain was found to have exceptionally high evolution rates [27].

Almost without exception, the two classes of genes (encoding pheromone/pheromone receptors and HD1/HD2 transcription factors) are part of the MAT locus in basidiomycetes, which is the only genomic region for which the sequence varies according to the mating type. A notable aspect of the tetrapolar system is that it is multiallelic with respect to at least one of the two genetically unlinked classes of MAT genes, resulting in up to thousands of different mating types in some species [2], [3], [16], [28], [29]. Bipolar systems are, on the contrary, usually biallelic for both classes of genes [30], [31].

Tetrapolar species can be found in all three major lineages of Basidiomycota interspersed with bipolar species [16], [32] and, most significantly, do not seem to be uniformly distributed. In the subphylum Agaricomycotina, which encompasses the mushrooms, the majority of the species seems to be tetrapolar [16]. The subphylum Ustilaginomycotina harbours many plant pathogenic species like U. maydis, most of which exhibit tetrapolar mating systems very similar to those found in the Agaricomycotina. A substantial body of evidence [3], [30], [33] suggests that in these two subphyla, the few bipolar species were derived from tetrapolar ancestors as a result of coalescence between the regions encoding the two classes of MAT genes, like in the human pathogens Cryptococcus neoformans [30] and Malassezia globosa [34] and the barley smut Ustilago hordei [31]. In other cases (the mushrooms Coprinellus disseminatus and Pholiota nameko) the transition to bipolar behaviour was due to loss of the association of the pheromone receptor to the MAT locus [35], [36]. The third subphylum, the Pucciniomycotina, contains about one-third of all species of Basidiomycota [37]. The majority of the species in the Pucciniomycotina are rust fungi, a large group of economically important obligate plant parasites. Classical mating studies indicate a predominance of bipolar systems in this subphylum both for rusts [38], other plant parasites like Microbotryum violaceum [39] and for saprobic yeasts of the genera Rhodosporidium and Sporidiobolus [40], [41]. However, detailed molecular analyses elucidating MAT gene content and function are very limited except for M. violaceum, in which size dimorphic sex chromosomes were identified and preliminarily characterized [42] and the pheromone receptor genes of both mating types were recently identified [43]. Since molecular phylogenies and ultrastructure suggest that Pucciniomycotina diverged first among subphyla of Basidiomycota [44], the elucidation of the genetic structure of the mating systems in this lineage is of major importance for understanding the origin and evolution of basidiomycete MAT loci.

The lack of knowledge on the sexual reproduction mechanisms of the Pucciniomycotina is mainly a consequence of the obligate parasitism of the rust fungi that seriously constrains experimental manipulation. This problem can be circumvented by studying related saprophytic organisms like those of the genera Rhodosporidium and Sporidiobolus since they are capable of completing their life cycle in culture. This led us to the recent characterization of one of the pheromone receptor regions in several bipolar red yeast species, including the heterothallic red yeast Sporidiobolus salmonicolor [45].

Here we report on the molecular characterization of the mating system in S. salmonicolor. We identified, for the first time in the Pucciniomycotina, the divergently transcribed genes encoding the HD1 and HD2 transcription factors and we investigated how HD1/HD2 transcription factors and the pheromone receptor system interact to produce the bipolar mating behaviour observed in S. salmonicolor. A new, non-bipolar non-tetrapolar, sexual mechanism was unveiled, in which occasional disruptions of the genetic cohesion of the bipolar MAT locus originate new mating types in a process that parallels that of tetrapolar systems.


Identification of MAT genes in both mating types of S. salmonicolor

We recently identified MAT A1 (see the Methods section for changes in mating type designations in S. salmonicolor) pheromone receptor and pheromone precursor genes in the heterothallic bipolar red yeasts Rhodosporidium toruloides and Sporidiobolus salmonicolor and in Sporobolomyces roseus [45]. These studies failed to uncover HD1/HD2 transcription factor genes in the vicinity of the pheromone receptor in any of the species studied. However, HD1 and HD2 homologs [32], [45] were found in the completely sequenced genome of Sporobolomyces roseus, but at a large distance from the pheromone receptor gene. To get some insight in the genetic structure of MAT loci in red yeasts, we set out to characterize the MAT genotype of a set of 36 S. salmonicolor strains. This species was chosen because of previous studies concerning its mating behaviour [46] and of the availability of a 3× genome coverage in the form of Trace Archive sequences for one MAT A1 strain, considerably facilitating the identification of novel genes.

We first identified the pheromone receptor gene in the complementary mating type of S. salmonicolor (MAT A2). Degenerate primers based on the sequences available for homologous MAT A2 receptors, including that of the closely related Rhodosporidium babjevae for which Trace Archive genomic sequences are available, failed to amplify the S. salmonicolor gene. An alternative approach was conceived, based on our previous observation of a high degree of synteny between the same mating type in different red yeast species [45]. For this, the region surrounding the pheromone receptor gene in R. babjevae was assembled stepwise using Trace Archive sequences and was subsequently scrutinized for the presence of genes exhibiting a higher degree of conservation across species than pheromone receptor genes. Two putative genes encoding an LSm-like protein (LSm7) and a ribosomal protein L6 (RibL6) were found respectively upstream and downstream of STE3.A2 in R. babjevae. Sequences homologous to these genes were readily found by BLASTN search in the S. salmonicolor Trace Archives but they were differently organized, since the sequenced strain (CBS 483) belongs to the opposite mating-type (MAT A1; Figure S1). PCR primers based on the S. salmonicolor LSm7 and RibL6 genes finally allowed the amplification of the intervening S. salmonicolor STE3.A2 gene (GenBank accession number GU474641), attesting synteny conservation between S. salmonicolor and R. babjevae in this region within the same mating type. As expected, the predicted amino acid sequence of the S. salmonicolor receptor exhibited the highest similarity with the sequences of the R. babjevae (54%) and M. violaceum (47%) homologues.

The divergently transcribed genes encoding the HD1 and HD2 transcription factors were identified in the Trace Archives sequences of S. salmonicolor using the homologous sequences of S. roseus. Primers based on the homeodomain conserved region of these genes amplified a fragment encompassing the highly variable 5′ regions of both genes as well as the intergenic region between the HD1 and HD2 genes (Figure S1). Homology to the HD1 and HD2 proteins from S. roseus was, as expected, limited to the homeodomain region since all functional HD proteins characterized so far were found to have highly variable N-terminal domains, even when different HD1/HD2 alleles from the same species are compared.

Allele number and mating-type specificity of HD1/HD2 and pheromone receptor genes in S. salmonicolor

Heterothallic red yeast species within the order Sporidiobolales were all described as having a bipolar behaviour in standard mating tests [40], [41]. Therefore, it was striking to notice that in S. roseus, the distance between the pheromone receptor and HD1/HD2 regions although still not accurately determined, was in any case larger than 800 Kb [32], [45].

Hence, if both classes of genes were part of a bipolar MAT locus with suppression of recombination over its entire length, it would be the largest such locus characterized so far in basidiomycetes. Such a region would nevertheless functionally resemble the MAT loci of C. neoformans [30], [47] and U. hordei [31], [48]. Alternatively, one of the compatibility check points might no longer be required to determine sexual identity, as previously observed for two mushroom species [35], [36]. In light of this, it was important to investigate how HD1/HD2 transcription factors and the pheromone receptor system interacted to produce the bipolar mating behavior. Isolation of both classes of MAT genes in S. salmonicolor enabled us to examine this question for the first time. We first used specific PCR primers to assess the correlation between the presence of the alternate pheromone receptor genes (STE3.A1 and STE.A2) and mating behavior, in 36 natural isolates of S. salmonicolor (Table S1). Without exception, STE3.A1 was present in MAT A1 strains, whereas the STE3.A2 receptor gene was found in MAT A2 strains. Hence, the pheromone receptor was clearly associated to mating behaviour. Next, PCR fragments encoding the 5′ portions of the HD1and HD2 genes were obtained from the 36 S. salmonicolor strains of both mating types and sequenced (GenBank accession numbers GU474649–GU474693). Surprisingly, instead of two HD1/HD2 alleles, each strictly linked to one of the mating types, as might be expected for a bipolar species, 13 HD1/HD2 alleles exhibiting substantial sequence divergence were uncovered (Figure 1A). Such numbers of HD1/HD2 alleles were previously observed only for tetrapolar species [16]. In U. maydis, for example, 33 HD1/HD2 alleles were identified [49] which do not have a particular association to either one of the two pheromone receptors because the two MAT regions are located on different chromosomes [3] and thus segregate independently at meiosis. On the contrary, in the bipolar species characterized so far, only two HD1/HD2 alleles are present, each of which is linked to one of the two pheromone receptors forming two large bipolar loci [30], [31]. Recombination between the two genetically linked MAT regions is suppressed in these species as a result of extensive sequence divergence, gene inversions and the accumulation of repetitive elements reminiscent of sexual chromosomes in animals and some plants [1], [30], [31], [50]. In S. salmonicolor, each of the 13 alleles always appears associated with the same receptor, suggesting some form of genetic linkage between the two regions (Figure 1). However, each receptor is associated with seven (Ste3.A2) or six (Ste3.A1) different HD1/HD2 alleles which is in sharp contrast with other bipolar species (Figure 1). There is apparently no bias regarding the geographic distribution of HD1/HD2 alleles, since strains carrying the same HD1/HD2 allele were isolated from very diverse locations worldwide (Table S1). To shed some light on the phylogenetic relationship between the HD1/HD2 alleles, we also examined the alleles present in a very closely related species, S. johnsonii. Several lines of evidence suggest that S. salmonicolor and S. johnsonii are undergoing a speciation process in which pre-zygotic barriers are absent, since crosses between sexually compatible strains of the two species normally yield dikaryotic mycelium and teliospores [46]. Intriguingly, extant allele diversity seems to have been generated after the onset of this incipient speciation event, as HD1/HD2 alleles from the two species are, in general, phylogenetically distinct (Figure S2). However, some incongruities between rDNA and MAT gene phylogenies can be observed (Figure S2), indicative of a certain degree of gene flow between the two species. For example, S. salmonicolor strain CBS 2634 has a S. johnsonii rather than a S. salmonicolor receptor allele and, in addition, a group of five S. salmonicolor strains carry HD1/HD2 alleles (A1–5, A2–16, A1–6; Figure S2) which seem to be phylogenetically more related to the S. johnsonii clade. The intraspecific common ancestry of HD1/HD2 alleles contrasts with the polymorphism observed for the pheromone receptor genes. The latter genes were found to exhibit a clear and ancient trans-specific polymorphism (Figure S3), as previously reported for M. violaceum [43].

Figure 1. Diversity and phylogeny of MAT gene alleles in S. salmonicolor.

(A) Phylogeny of HD1/HD2 genes. Mating types A1, A2, and asexual strains are designated as A1, A2 and AS, respectively. Boxes designate the various HD1/HD2 alleles with numerals after the mating type designation. Circles after strain numbers depict the type of pheromone receptor gene (yellow, STE3.A1; blue, STE3.A2). Asterisks indicate the two instances where common ancestry of HD1/HD2 alleles associated with opposite mating types is best supported. (B) Comparison of the number and distribution of MAT gene alleles in emblematic species representing the different mating systems (HD, homeodomain region; PR, pheromone receptor region; the continuous or discontinuous line between the HD and PR boxes denotes genetic linkage or its absence, respectively).

Hence, the relationship between mating type and HD1/HD2 allele number and distribution is unexpectedly complex in S. salmonicolor, and the possibility that the HD1/HD2 transcription factors might have recently lost their linkage to MAT and are no longer involved in determining sexual compatibility in this species could not be readily discarded. To examine this, we determined first the evolution rates (dN/dS) of nine HD1 alleles of S. salmonicolor and S. johnsonii (GenBank accession numbers GU474694–GU474702). Prior studies in the mushroom Coprinus cinereus brought to light exceptionally high evolution rates for the domains in HD1 proteins involved in self/non-self recognition [27]. We observed even higher evolution rates for the homologous domains in the HD1 proteins of S. salmonicolor (>1 in some segments, indicative of adaptive selection; Figure 2 and Figure S4), which constituted the first evidence that these transcription factors contribute to determine sexual compatibility in S. salmonicolor, together with the pheromone receptor system.

Figure 2. Evolution rate of the HD1 gene in S. salmonicolor.

Synonymous (dS), non-synonymous (dN) and dN/dS average values for all pairwise comparisons between nine alleles of the HD1 gene. Y axis – evolution rates; X axis – base pairs of HD1 coding region. Average values are given for the highly variable N-terminal domain which is involved in non-self recognition, and for the more conserved homeodomain (HD) and C-terminal domains.

A pseudo-bipolar mating system

We sought further for an explanation of how the “one-to-many” ratio between pheromone receptor and HD1/HD2 genes, characteristic of tetrapolar systems, results in bipolar behaviour with only two mating types in S. salmonicolor. To this end, we investigated the possibility that the cohesion of the bipolar MAT locus in S. salmonicolor might be occasionally disrupted, giving rise to new receptor/HD allele combinations. Such recombination events would explain the common ancestry of extant A1- and A2-linked HD1/HD2 alleles (Figure 1A) and indeed the fact that all HD1/HD2 alleles in the species seem to share a common ancestor more recent than the formation of the species itself (Figure S2). Therefore, bipolarity in S. salmonicolor could be a consequence of the scarcity of recombination events on the one hand and of the exceptionally high evolution rates of HD1/HD2 proteins on the other hand. The combination of these two factors would lead to the association of each extant HD1/HD2 allele with only one of the alternate receptors, the hallmark of bipolarity. Alternatively, it could not be readily excluded that the observed apparent linkage could be due to population genetic phenomena related to the frequency of sexual reproduction and population size. To address the possibility of partial genetic linkage between the two MAT regions, we studied in detail the latter stages of the sexual cycle (germination of teliospores with the formation of basidia and basidiospores; Figure S5) in one cross between strains ML 2241 (MAT A1) and CBS 6832 (MAT A2). The progression through meiosis was microscopically monitored showing that although four nuclei could be observed after meiosis, only two basidiospores were formed, each arising from one of the two basidial compartments (Figure S5B). The two basidiospores were always found to be binucleate and they typically exhibited asynchronous germination (Figure S5). The molecular mating types of the progeny of eight meioses from the same cross were examined by micromanipulation of teliospores in the initial stages of germination. Several colonies isolated from each germinating teliospore were analysed and, in only one of the eight events examined (T1), were the two versions of the parental mating type genes recovered (Figure 3). Our interpretation is that the asynchronous germination of the two basidiospores results in a very strongly biased composition of the colony towards descendants of the basidiospore that germinates first. Micromanipulation of the basidiospores instead of the germinating teliospore would probably be required to recover the germination products of both basidiospores with higher frequency, but this proved to be technically very difficult due to the fact that germination takes place inside the agar and the structures to be manipulated are friable. Furthermore, the various colonies examined for each teliospore are most likely mitotic clones, as they invariably shared the same parental allele of the DMC1 gene, (Figure 3, GenBank accession numbers HM133872–HM133874). In six of the meiotic events examined, linkage between the pheromone receptor and the HD1/HD2 regions was maintained, as would be expected in a bipolar system (Figure 3). Germination of one additional teliospore yielded a strain which was apparently diploid since it carries pheromone receptor and HD1/HD2 alleles from both parental strains (Figure 3) and has a self-fertile phenotype with the formation of mycelium and teliospores. Self-fertile and asexual strains can be found among natural isolates of red yeasts of the Sporidiobolales [40], [41] and the origin of the first may be related to the occasional formation of diploid yeast strains. In addition to our present observations, the formation of diploid strains was also previously reported in R. toruloides [51]. However in none of the species studied so far are these diploid states prevailing, leading to the presumption that although these strains do not exhibit obvious growth defects, their genetic makeup may carry some selective disadvantages. Moreover, our preliminary observations suggest that teliospores formed by the S. salmonicolor diploid strain do not germinate, which argues against the co-existence of homothallic and heterothallic life styles in this species. Interestingly, the type strain of S. johnsonii (CBS 5470T) may have originated from a diploid strain because it carries both pheromone receptor alleles. However, only one HD1/HD2 gene pair is present which may indicate that a self-compatible HD1/HD2 gene pair was generated by recombination between the two parental alleles (Figure S2). The type strain of S. johnsonii is homothallic [41], [46] but does not form basidia, differing in that respect from all the other strains of this species, which carry only the MAT A1 receptor gene and are in general capable of mating with S. salmonicolor MAT A2 strains.

Figure 3. Segregation analysis of the STE3 and HD1/HD2 genes after meiosis.

(A) T1 to T8 refer to 8 individually germinated teliospores obtained by micromanipulation from the cross between strains CBS 6832 (A2–15) and ML 2241 (A1–3). The result of the diagnostic PCRs for the presence of the alternate STE3.A1 and STE3.A2 genes and the identification of HD1/HD2 amplicons by Rsa I digestion is shown. Screening of the parental origin of the DMC1 allele by PCR and digestion with Msp I show clonality of the various colonies examined for each teliospore. For each germinated teliospore, three to six colonies were studied. With the exception of teliospore T1, only one mating type was recovered per meiosis presumably due to asynchronous germination of basidiospores (see Figure S5C). Teliospore T8 yielded a strain which is apparently diploid, and the new mating type was recovered from teliospore T7.

One germinated teliospore yielded the most striking result, since it produced an haploid strain in which recombination occurred, causing the HD1/HD2 allele of parental strain CBS 6832 (MAT A2) to become associated with the Ste3.A1 receptor (Figure 3), a combination that is not found among natural isolates (Figure 1A). The new mating type (strain T7) was unable to complete the sexual cycle when crossed with either parental strain (Figure 4). A cross with the parent sharing the same pheromone receptor gene resulted in a complete failure to switch to filamentous growth, whereas homozygosity at the HD1/HD2 region precluded progression through the sexual cycle, but allowed some pseudohyphal growth, probably as a result of cell-cell pheromone signalling (Figure 4). This demonstrates unequivocally that both compatibility regions are required for sexual reproduction in S. salmonicolor. The new mating type did not show obvious defects in vegetative growth, exhibiting growth rates in synthetic and complete media similar to those of the parental strains (results not shown). It also had normal sexual proficiency when crossed with strains carrying different alleles at both MAT regions (Figure 4), forming dikaryotic mycelium with teliospores that germinate normally (result not shown).

Figure 4. Sexual proficiency of T7.1, the new mating type of S. salmonicolor.

For each cross the top section indicates the type of cross and the strains involved. Micrographs of crosses (4 days of incubation at 25°C on corn meal agar) are shown in the middle section (inserts depict details in higher magnification to show the presence or absence of teliospores). The bottom section shows the STE3 and HD genotypes of each strain and the outcome of the cross evaluated by the presence (+) or absence (−) of mycelium with clamp connections and teliospores.

Recombination between the two classes of MAT genes seems to be possible but infrequent, a situation that, to our knowledge, has never been described before in basidiomycetes and can be regarded as intermediate between bipolar and tetrapolar systems. Therefore, this observation called for a closer examination of the meiotic events described above. In particular, it was important to establish how genetic markers unrelated to MAT segregated in these meiotic events, thereby getting some insight in the recombination frequency characteristic of this species in autosomal regions while simultaneously confirming that a normal meiosis had taken place in all the cases examined. It should be noted that a more precise determination of recombination frequencies and a statistically significant demonstration of linkage between genomic regions would require the examination of a larger number of meiotic products, but nevertheless examination of the eight available strains yields significant information concerning recombination inside and outside the MAT region. To characterize the haploid progeny strains, we chose nine genes located in four different S. roseus scaffolds (Figure 5). Pairs of genes located on the same scaffold were at distances ranging between 0.525 and 1.87 Mb from each other (Figure 5B). The selected genes were partially amplified in the two parental strains used in this cross (ML 2241 and CBS 6832) and sequence polymorphisms were scored which allowed the two parental alleles to be distinguished and their fate after meiosis to be tracked (GenBank accession numbers HM133857–HM133883). Sequencing of this set of genes in the seven haploid progeny strains confirmed that these markers segregate independently of MAT-specific genes (Figure 5). Markers located more than 1.2 Mb apart seem to be genetically unlinked, while the results suggested partial linkage for genes that are 525 to 920 kb apart, with an average of 32 kb/cM for these autosomal regions. The scaffolds containing the two MAT regions were subsequently subjected to a similar analysis. In scaffold 7, five genes, including the HD1/HD2 pair were found to contain polymorphisms and were studied with respect to their parental origin in the seven haploid progeny strains (GenBank accession numbers GU474757–GU474780, HM133833–HM133856). In the scaffold harbouring the STE3 gene, the parental origin of a total of eight additional genes exhibiting polymorphisms was determined (GenBank accession numbers GU474709–GU474756, HM133785–HM133832). The relative orientation of the two scaffolds could not be previously established [45], but the results of our scrutiny of meiotic recombination in these regions suggest linkage between the IsocL gene in scaffold 7 and the PAN6 gene in scaffold 9. This implies that the relative orientation of the two scaffolds is most likely as depicted in Figure 5A. The analysis of the markers in these regions brought to light, in addition to sites where probably crossovers occurred, several instances where very likely gene conversion took place instead, one of which curiously involves the HD1/HD2 gene pair (Figure 5A). In line with this, we found that the phylogeny of several genes located in the two scaffolds harbouring MAT genes also occasionally denotes signs of past gene conversion events when multiple strains of S. salmonicolor and S. johnsonii are examined (Figure S6). For example, the LSm7 gene located close to STE3, exhibits an unusual mosaic phylogeny, which is species-specific in most of the gene but is MAT specific at the 3′-end, proximal to STE3 (Figure S6). This suggests that this gene may have integrated the MAT locus long ago as might be expected from its close proximity to a key MAT-specific gene, but that the 5′end underwent conversion more recently, after incipient separation of the two species. Phylogenetic analysis of the RibL18ae, RNAPOL, NGP1 and AKOR2 genes also suggests gene conversion events in S. salmonicolor strain CBS 1012 (Figure S6). These observations support the idea that gene conversion is an important mechanism to maintain species-specific sequences at the S. salmonicolor MAT locus. This may, in turn, reflect the need to counteract the effect of recombination suppression which could lead to mating type-linked deleterious mutations. It is also important to note that sequence divergence between mating types of genes located in the vicinity of the receptor/pheromone MAT region is much lower in the red yeasts examined than, for example in Cryptococcus neoformans (Figure S6, [47]), although in the later species some events of gene conversion within the MAT loci have also been noticed [47].

Figure 5. Analysis of meiotic progeny.

(A) Genomic regions surrounding the HD1/HD2 and pheromone receptor genes in S. salmonicolor MAT A1. Genes in the immediate vicinity of STE3.A1 are depicted as block arrows to denote the direction of transcription. The same genes are highlighted with an orange box. Synteny with the homologous genomic region of S. roseus was confirmed for all genes except those shown as empty arrows (depicted in the arrangement present in S. roseus). Outside the highlighted region, genes present in the same S. roseus scaffold at different distances (indicated by the arrows) from STE3.A1 were selected. Four genes were similarly selected from the HD1/HD2 scaffold, assuming synteny with S. roseus. For eight independent teliospores (T1–T8) the parental origin of the genes is indicated. Genes from strain ML 2241 (A1–3) are shown in green and those from strain CBS 6832 (A2–15), in red. Asterisks mark sites were crossovers were detected. Possible gene conversion events are marked with “C”. The two scaffolds are depicted in the most likely orientation. The region shadowed in light yellow encompasses the putative pseudo-bipolar MAT locus in S. salmonicolor MAT A1. (B) Segregation patterns and recombination frequencies (RF) of nine autosomal markers located in four different scaffolds. The position and relative distances between the genes are depicted as in S. roseus genome. T8 is a diploid strain since it contains both parental alleles for all genes tested.

Three crossovers were mapped to a region of 27 kb adjacent to the HD1/HD2 gene pair (T5, T6 and T7; Figure 5), which seems to configure a hotspot for recombination (0.63 kb/cM) when compared with the average frequency of recombination observed for the autosomal regions examined (∼32 kb/cM). Interestingly, hotspots have been mapped close to the borders of the MAT locus in Cryptococcus neoformans [52] and were proposed to play an important role in the evolution of these specialized genomic regions. Three recombination events were also detected on the opposite side of the putative MAT locus in a region of ∼220 kb (T1, T2 and T3; Figure 5) but in this case only one genetic marker (MIP) was studied on one side of this position, which makes it difficult to distinguish between gene conversion and crossover events. Finally, two crossovers were detected in the proximity of the PAN6 gene, one of which was the cause of the only instance of recombination detected between the STE3 and the HD1/HD2 genes (T7, Figure 5). In the other case (T4, Figure 5), the MAT A1 parental mating type prevailed, due to apparent gene conversion involving the HD1/HD2 gene pair. In the 1.2 Mb region between the HD1/HD2 and PAN6 genes no crossovers seem to have occurred, suggesting that recombination frequency is lower than average or possibly suppressed in this region.

Hence, we propose that in S. salmonicolor a new type of fungal sex determining region operates, which is neither tetrapolar nor strictly bipolar. S. salmonicolor seems rather to have a large pseudo-bipolar MAT locus in which recombination in the region between the two MAT regions is infrequent but not suppressed, allowing for occasional disruptions of its genetic cohesion. The proposal of an intermediate system between bipolar and tetrapolar is based mainly on two kinds of observations, which are in line with each other. Firstly, the allelic distribution and number of MAT genes depicted in Figure 1 outlines a situation that is itself intermediate between bipolar and tetrapolar (multiple HD1/HD2 alleles but only two mating types). Secondly, when trying to clarify this new finding, we found that recombination may occur in the intervening region between the two MAT regions, which provides a likely and plausible explanation for the observed resemblance with tetrapolar systems in what concerns evolution and number of HD1/HD2 alleles. On the other hand, the genomic region around the receptor/pheromone locus exhibiting synteny breaks, gene inversions and sequence divergence between the two mating types is significantly larger in S. salmonicolor than in tetrapolar species with similar numbers of MAT gene alleles, like U. maydis (Figure S1, [47]). We envisage that the offspring of the relatively rare events of meiotic recombination in the MAT locus of S. salmonicolor can be rescued from reproductive isolation by the existence of multiple HD1/HD2 alleles associated to each of the two alternate receptors in natural populations. In such a pseudo-bipolar system, negative frequency-dependent selection could operate to preserve HD1/HD2 allele diversity and explain the exceptionally high evolution rates of HD1 proteins.

A model for the evolution of MAT loci in basidiomycetes

Both the content and the organization of the basidiomycete MAT loci are unlike all other fungi, because compatibility is encoded in the MAT locus itself, while in other fungi the genes present in the MAT locus regulate expression of pheromones and pheromone receptors that are encoded elsewhere in the genome. The available data does not suffice to address definitively the question of how the basidiomycete MAT locus arose, but one hypothesis has been recently put forward that postulates that the pheromone receptor and/or the HD systems may have evolved in a self compatible manner [49]. The emergence of self-incompatible alleles by mutation or recombination could have subsequently laid the basis for the emergence of the tetrapolar system. There is currently insufficient evidence, also including our present observations, to state decisively whether the ancestral basidiomycete mating system was initially bipolar or tetrapolar, at the onset of the involvement of both the HD and pheromone receptor systems in determining mating specificity. However, our observations concerning the mating system in S. salmonicolor, suggest that novel and useful insights may be gained in this respect by a wider phylogenetic sampling of mating systems in the Pucciniomycotina.

In line with this, we subsequently looked into the HD1/HD2 allelic distribution of Rhodosporidium babjevae, another bipolar red yeast species phylogenetically related to S. salmonicolor. Also in this case, multiple HD1/HD2 alleles were associated with each receptor (Figure S7). Since this allelic distribution is the hallmark of the pseudo-bipolar system, we conclude that rather than being an oddity restricted to S. salmonicolor, this system is likely to operate in many of the yeast species of the order Sporidibolales [53] and probably also in other members of the subphylum Pucciniomycotina that were thus far thought to be bipolar. The most parsimonious explanation for this is, in our view, that a very similar system was present in the common ancestor of Rhodosporidium and Sporidiobolus. This implies that pseudo-bipolarity it is not a short-lived transitional mating system, like those presumed to have marked the transition to the bipolar state in C. neoformans [30], [31] and U. hordei [3]. Rather, it suggests that it may be evolving from an ancestral system in which the two classes of MAT genes were located on the same chromosome, but of which it is not possible to infer from currently available data whether the two MAT regions were genetically linked. The model shown in Figure 6 depicts the possibility that the ancestral basidiomycete mating system may have been similar to the pseudo-bipolar system found in S. salmonicolor. We highlighted this possibility among others, because the Pucciniomycotina is the earliest derived basidiomycete lineage and seems therefore more likely that members of this group have retained mating systems akin to the common ancestral system. In this scenario, the Pucciniomycotina would have diverged before the stabilization of the tetrapolar system (with the two MAT regions on different chromosomes), which is presumed to be the ancestor of the mating systems in the other two lineages (Ustilaginomycotina and Agaricomycotina) [49].

Figure 6. The pseudo-bipolar system and the evolution of MAT loci in Basidiomycota.

The ancestral basidiomycete mating system may have been similar to the pseudo-bipolar system found in S. salmonicolor. The classic tetrapolar system emerged in the common ancestor of the Ustilaginomycotina and Agaricomycotina through a chromosomal translocation that placed the two MAT regions on different chromosomes. In U. hordei and C. neoformans a second translocation may have triggered a precipitous transition to bipolarity, as previously proposed [3], [33]. In the mushroom Co. disseminatus, the pheromone receptor (white box) ceased to be associated to MAT leading to bipolarity. Mating systems in the Pucciniomycotina may have evolved to extant systems exhibiting partial (S. salmonicolor) or complete (M. violaceum) suppression of recombination between the two MAT regions. Tetrapolar systems in this lineage might be present in Leucosporidium scottii and the rusts (Uredinales) but have not been characterized at the molecular level yet. In these systems, MAT regions may be distantly located on the same chromosome or on different chromosomes. The number of MAT gene alleles identified in each species is shown next to the boxes representing the homeodomain (HD) and pheromone receptor (PR) regions. Stripes between the HD and PR regions denote reduced or suppressed recombination.

The model proposed in Figure 6 depicts this possibility and accommodates the possible occurrence of abrupt as well as gradual transitions to bipolar mating behaviour, the first but not the second being triggered by gross genomic rearrangements.


An intermediate, pseudo-bipolar mating system entails odds of inbreeding which are in between those observed for the bipolar and tetrapolar systems (50% and 25%, respectively; [33]). This may provide for some species the right balance between genetic stability (imparted by inbreeding) and variation (favoured by outcrossing) and may, in turn, delay the attainment of a strictly bipolar state if a system is drifting away from a tetrapolar configuration without abrupt occurrences, such as large chromosomal rearrangements. Our time course microscopic observation of meiotic events in S. salmonicolor indicates that basidiospores exhibit asynchronous germination (Figure S5C), decreasing the probability of a cross between siblings immediately after meiosis. This, together with the occasional meiotic recombination events, would generally decrease the odds of selfing when compared with a typical bipolar system, like that of the phylogenetically related plant pathogen Microbotryum violaceum [39]. Hence, the pseudo-bipolar mating system emerges as a remarkable novel context in which to explore how life-style, ecology and modes of reproduction interplay in the evolutionary history of eukaryotes.


Strains and mating-type designations

The list of strains studied and relevant information associated to them is given in Table S1. We re-assigned mating type designations of S. salmonicolor in order to match the “molecular mating type” identified by PCR detection of the pheromone receptor alleles (STE3.A1 or STE3.A2).

Common settings for PCR amplification

Preparative PCR reactions were performed in a final volume of 50 µl with the following components (unless stated otherwise): 2 mM of MgCl2, 0.20 mM of each of the four deoxynucleoside triphosphates (GE Healthcare), 1% DMSO, 0.8 µM of each primer, 100 ng of genomic DNA, and 1 U Taq DNA polymerase (Fermentas, Canada). Thermal cycling consisted of a 5-minute denaturation step at 95°C, followed by 35 cycles of denaturation at 94°C for 30 s, 30 s at the annealing temperature (variable), and extension at 72°C (variable time). For annealing temperatures, extension times and primer sequences see Table S2. A final extension of 7 min at 72°C was performed at the end of each reaction.

PCR amplification and sequencing of the MAT A2 pheromone receptor (STE3.A2 allele) in S. salmonicolor

The pheromone receptor gene (pr-MatA2) from Microbotryum violaceum (GenBank accession number EF584741) was used to perform a BLASTN search in the NCBI Trace Archive sequences of the genome project of Rhodosporidium babjevae strain WP1 (MAT A2; The complete STE3.A2 sequence of R. babjevae, in addition to the flanking regions, were assembled (Table S3) and subsequently scrutinized for the presence of genes exhibiting a higher degree of conservation across species than pheromone receptor genes. Sequences of two putative genes encoding an LSm-like protein (LSm7) and a ribosomal protein L6 (RibL6) were used to design a pair of degenerate primers (MC122 and MC123) to amplify and sequence the intervening region in S. salmonicolor MAT A2 strain CBS 490T. This region contained the STE3.A2 S. salmonicolor gene, which was sequenced by primer walking using primers MC126 and MC127 (Figure S1).

PCR amplification and sequencing of the HD1/HD2 region in S. salmonicolor

Using the sequence of the HD1 gene of Sporobolomyces roseus [45], a BLASTN search was performed in the NCBI Trace Archive database of S. salmonicolor and positive hits (Table S3) were assembled into a complete HD1 gene. The upstream flanking region of the HD1 was assembled stepwise and inspected using AUGUSTUS software [54], revealing the presence of a divergently transcribed HD2 homologue. The deduced protein sequences of HD1 and HD2 of S. roseus and S. salmonicolor were aligned and the conserved regions were used to design specific primers (MC103 and MC104) to amplify and sequence the corresponding N-terminal and intergenic regions of the HD1/HD2 genes in all S. salmonicolor and S. johnsonii strains (Figure S1, Table S3).

Correlation between mating behaviour and the presence of pheromone receptor genes

To confirm mating behavior and sexual compatibility, 2–4 day-old cultures were crossed on corn meal agar (Difco), incubated at room temperature for 1 week, and examined microscopically using phase-contrast optics for production of mycelium with clamp connections and teliospores. Diagnostic PCR with primers for STE3.A1 (MC053 and MC054) and STE3.A2 (MC126 and MC127) were carried out to identify the pheromone receptor genes.

Germination of teliospores and microscopic monitoring of meiosis in S. salmonicolor

Strains CBS 6832 (A2–6) and ML 2241 (A1–3) were mixed on corn meal agar (Difco) and incubated at room temperature (∼22°C) for 2 weeks, to allow for abundant production of teliospores. Small (∼0.5 cm) agar blocks containing teliospores were soaked in sterile distilled water for 8–10 weeks at 4°C. After this resting period, a suspension of teliospores was obtained by gently mashing the agar blocks with a small pestle. Teliospore germination was induced by transferring this suspension to 2% low melting point (LMP)-agarose plates incubated at room temperature for 2 weeks. To follow the germination of selected teliospores, small drops of the same suspension were transferred to 2% LMP-agarose-coated-slides. The different stages of meiosis were observed microscopically by staining several germinating teliospores with Safranin O [55]. Observations were made daily with 100× magnification using a Leica DMR microscope equipped with brightfield and differential interference contrast optics and microphotographs were recorded using a Leica DFC320 digital camera (Leica Microsystems GmbH, Wetzlar).

Micromanipulation of teliospores and segregation analysis in S. salmonicolor

Teliospores resulting from the cross of strains CBS 6832 (A2–6) and ML 2241 (A1–3) were germinated as described above. Using a micromanipulator, teliospores in the initial stages of germination, i.e. with a non-septate basidium initial, were individually separated, transferred to MYP agar [46] and incubated at room temperature. The colony that formed after 1–2 days was re-streaked to obtain colonies derived from single cells. In three to six of these colonies, segregation of the two MAT regions was assessed by diagnostic PCR with specific primers for STE3.A1 (MC053 and MC054), STE3.A2 (MC126 and MC127) and HD1/HD2 (MC103 and MC104). The HD1/HD2 alleles were discriminated after amplification by digestion with restriction enzyme Rsa I.

Sequence data and phylogenetic analyses

DNA and protein sequences were aligned with ClustalW 1.81 [56] with minor manual corrections. For the phylogeny of HD1/HD2 alleles, FindModel (, which is an implementation of ModelTest [57], with the Akaike information criterion (AIC) was used. The Tamura-Nei (TrN)+G model [58], [59] (shape parameters 0.98049 and 1.08652 in Figure 1 and Figure S2 datasets, respectively) was employed in MEGA4 [60] using the Neighbor-Joining algorithm [61] and bootstrap values from 1000 replicates. For the phylogeny of the pheromone receptors (Figure S3) the substitution model of protein evolution was selected using ProtTest [62] with AIC. The WAG+I+G [59], [63], [64] model (shape parameter = 2.99; proportion of invariable sites = 0.035) was employed in PHYML [65] using maximum likelihood and bootstrap values from 100 replicates.

Estimation of the evolution rates of the HD1 gene

To obtain the sequence of the 3′end of HD1 gene the region encompassing the homeodomain and a conserved motif located 10 bp upstream of the STOP codon was amplified using primers MC111 and MC112. The 5′end of the HD1 gene was amplified using primers MC103 and MC104 (Figure S1). Evolution rates were estimated by a Window Analysis of dN and dS, using the online interface of WINA 0.34 [66], in a sliding window (size = 20) along the alignment of nine HD1 alleles.

Mating type specificity and phylogenetic analysis of genes located at variable distances from the HD1/HD2 and the pheromone receptor regions in S. salmonicolor

Based on the available genomic information of the closely related species Sporobolomyces roseus, and assuming that synteny is maintained in S. salmonicolor [41], eight genes from the pheromone receptor region (scaffold 9) and four genes from the HD1/HD2 region (scaffold 7) were selected. NCBI S. salmonicolor Trace Archive sequences of these genes were obtained (Table S3) and assembled. Primers were designed for partial sequencing of these genes (Table S2). Protein-coding DNA sequences were deduced after removal of putative introns, either manually or using AUGUSTUS software [54], automatically aligned using ClustalW and manually edited according to the superimposed amino acid sequences. Synonymous substitutions (dS) values and the divergence percentage between mating type-specific alleles were calculated using DnaSP 5.0 [67] for a set of 10 S. salmonicolor strains (Figure S6). Phylogenies were obtained in MEGA4 [60] using Maximum Parsimony (MP), with the close-neighbor interchange algorithm for heuristic searches and bootstrap values from 1000 replicates.

Genotyping of the meiotic progeny

To detect differences among the meiotic progeny, we selected nine genes located on four different scaffolds (1, 2, 3 and 10; Figure 5) in the S. roseus genome. Sequences of these genes in S. salmonicolor were assembled from the NCBI Trace Archive (Table S3) and primers were designed to amplify partial sequences in parental strains CBS 6832 and ML 2241 (Table S2). Sequence polymorphisms were scored and used to track the parental origin of the alleles in all the meiotic progeny. This analysis was performed either by PCR and sequencing or by RFLP analysis (Table S2). The genes previously used to obtain mating type-specific phylogenies were similarly assessed in this genotyping analysis.

Supporting Information

Figure S1.

Organization of the genomic regions containing the pheromone receptor (STE3) and the HD1/HD2 genes in S. salmonicolor. (A) Pheromone receptor region. Homologous genes are represented with the same colour. The pheromone genes (SsRHA1, SsRHA2 and SsRHA3) are shown only in MAT A1 because their position in MAT A2 strains is currently unknown. Primers used to obtain the complete sequence of the S. salmonicolor STE3.A2 gene are depicted by arrowheads. (B) The HD1/HD2 region comprises two divergently transcribed homeodomain genes. The homeodomain motifs are indicated as black boxes and an intron present in the HD2 gene is depicted. Black arrowheads indicate the position of the primers used to amplify the HD1/HD2 region.


(0.43 MB TIF)

Figure S2.

Phylogeny of HD1/HD2 alleles in the species complex S. salmonicolor/S. johnsonii. Mating types A1, A2, and asexual strains are designated as A1, A2 and AS, respectively. Boxes designate the various HD1/HD2 alleles with numerals after mating type designation. Yellow boxes correspond to HD1/HD2 alleles associated to the pheromone receptor gene STE3.A1 and blue boxes correspond to those associated with STE3.A2. Circles after strain numbers depict the type of pheromone receptor gene (yellow, STE3.A1; blue, STE3.A2). Half-coloured circles or boxes are used for S. johnsonii alleles. Lateral bars delimit S. salmonicolor (solid bar) and S. johnsonii (dashed bar) as defined by rDNA phylogeny [46]. The type strain of S. johnsonii (self-fertile) possesses both receptor genes STE3.A1 and STE3.A2. Asterisks indicate the two instances where (post-speciation) common ancestry of HD1/HD2 alleles associated with opposite mating types is best supported.


(0.86 MB TIF)

Figure S3.

Phylogeny of pheromone receptors in the Basidiomycota. (A) Phylogeny and estimated time of divergence based on that of Devier et al. [43]; 450 MY, represents the divergence between ascomycetes and basidiomycetes and 370 MY, corresponds to the divergence between the pheromone receptor alleles in Microbotryum violaceum. The phylogeny was estimated by PHYML 3.0 using representative species of the major lineages in the Basidiomycota. Numbers on branches represent statistical support using 100 bootstraps replicates (see Methods for details). Coloured circles depict phylogenetic groups as defined in the rDNA phylogeny [15] shown in (B). Sequence accession numbers are indicated in brackets after species names.


(0.74 MB TIF)

Figure S4.

Alignment of the HD1 proteins of S. salmonicolor and S. johnsonii. Alignment of the nine deduced protein sequences used in the evolutionary rates analysis (dN/dS). Coloured bars indicate the same three domains of the HD1 protein as in Figure 2. Sequences marked with an asterisk belong to the sibling species S. johnsonii.


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Figure S5.

Life cycle of Sporidiobolus salmonicolor. (A) Diagrammatic representation of the saprobic life cycle of S. salmonicolor. (B) Different stages of teliospore germination and formation of basidia and basidiospores; nuclei were stained with safranin O and are indicated by arrows: (i) initial stage of teliospore [Ts] germination with diploid nucleus and basidium initial [Ba]; (ii) migration of the diploid nucleus to the immature basidium; (iii) first meiotic division; (iv) formation of septum [Sp] originating a two-celled basidium; (v) second meiotic division yielding four nuclei; (vi) formation of two large binucleated basidiospores [Bs]; (vii) haploid uninucleated vegetative yeast cells [vc] resulting from basidiospore germination. Bars = 2.5 µm. (C) Time course observation of asynchronous germination of the basidiospores (i–iii). Note that, contrary to the basidiospore on the left, the basidiospore on the right formed yeast cells. Bars = 5 µm.


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Figure S6.

Phylogeny of several genes located in the two scaffolds harbouring MAT genes. The phylograms represent the single most likely tree for the selected genes located in the STE3 region (A) and in the HD1/HD2 region (B). Trees were generated under the close-neighbor interchange algorithm in a heuristic search. Numbers on branches indicate statistical support calculated from 1000 bootstrap replicates. Possible gene conversion events are marked with an asterisk after the strain number. For the majority of the genes, sequences of strains of MAT A2 (indicated by blue circles) are highly similar. In contrast, MAT A1 strains exhibit more sequence divergence, suggesting the existence of two lineages within this mating type (strains indicated by yellow and orange circles). Half-colored circles indicate S. johnsonii strains. Colored-shaded trees depict genes with sequence divergence clearly associated with mating type in S. salmonicolor. The position of the LSm7 gene (light pink) relative to the STE3 gene is shown for both mating types. Values for synonymous substitutions (dS) and divergence percentage (Dxy, %) are given for all genes (except for STE3) and in each pair comparisons.


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Figure S7.

Phylogeny of HD1/HD2 alleles in Rhodosporidium babjevae. The pheromone receptor gene (STE3.A1, yellow circles; STE3.A2, blue circles) and sequence accession numbers (in brackets) are indicated after strain number. The tree was reconstructed with Neighbour-joining and TrN+G model (shape parameter = 1.68453). Bootstrap values (>50%) from 1000 replicates are shown. S. salmonicolor and S. johnsonii are included for comparison.


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Table S1.

List of S. salmonicolor and S. johnsonii strains used in this study and relevant information pertaining to them.


(0.73 MB PDF)

Table S2.

List of primers, specific PCR conditions, and restriction enzymes used for the RFLP analysis.


(0.50 MB PDF)

Table S3.

NCBI Trace Archives sequences used in this study.


(0.73 MB PDF)


We thank V. Robert and M. Groenewald (CBS, The Netherlands) and C. P. Kurtzman (NRRL, USA) for providing strains.

Author Contributions

Conceived and designed the experiments: MAC JPS PG. Performed the experiments: MAC. Analyzed the data: MAC JPS PG. Contributed reagents/materials/analysis tools: JPS PG. Wrote the paper: MAC JPS PG.


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