• We are sorry, but NCBI web applications do not support your browser and may not function properly. More information
Logo of plosgenPLoS GeneticsSubmit to PLoSGet E-mail AlertsContact UsPublic Library of Science (PLoS)View this Article
PLoS Genet. Jun 2009; 5(6): e1000533.
Published online Jun 26, 2009. doi:  10.1371/journal.pgen.1000533
PMCID: PMC2694357

Evolution of Mutational Robustness in the Yeast Genome: A Link to Essential Genes and Meiotic Recombination Hotspots

Harmit S. Malik, Editor

Abstract

Deleterious mutations inevitably emerge in any evolutionary process and are speculated to decisively influence the structure of the genome. Meiosis, which is thought to play a major role in handling mutations on the population level, recombines chromosomes via non-randomly distributed hot spots for meiotic recombination. In many genomes, various types of genetic elements are distributed in patterns that are currently not well understood. In particular, important (essential) genes are arranged in clusters, which often cannot be explained by a functional relationship of the involved genes. Here we show by computer simulation that essential gene (EG) clustering provides a fitness benefit in handling deleterious mutations in sexual populations with variable levels of inbreeding and outbreeding. We find that recessive lethal mutations enforce a selective pressure towards clustered genome architectures. Our simulations correctly predict (i) the evolution of non-random distributions of meiotic crossovers, (ii) the genome-wide anti-correlation of meiotic crossovers and EG clustering, (iii) the evolution of EG enrichment in pericentromeric regions and (iv) the associated absence of meiotic crossovers (cold centromeres). Our results furthermore predict optimal crossover rates for yeast chromosomes, which match the experimentally determined rates. Using a Saccharomyces cerevisiae conditional mutator strain, we show that haploid lethal phenotypes result predominantly from mutation of single loci and generally do not impair mating, which leads to an accumulation of mutational load following meiosis and mating. We hypothesize that purging of deleterious mutations in essential genes constitutes an important factor driving meiotic crossover. Therefore, the increased robustness of populations to deleterious mutations, which arises from clustered genome architectures, may provide a significant selective force shaping crossover distribution. Our analysis reveals a new aspect of the evolution of genome architectures that complements insights about molecular constraints, such as the interference of pericentromeric crossovers with chromosome segregation.

Author Summary

Sexual life cycles constitute a costly alternative to vegetative modes of reproduction. Two categories of hypotheses seek to explain why sexual life cycles exist: those investigating the selective advantages that have driven the evolution of individual parts of this life cycle and those rationalizing the advantages sexual life cycles may offer as a whole, e.g., in extant species. Sex and recombination can be understood as efficient ways to interact with mutations and their consequences. Mutations occur at random and are mostly either deleterious or neutral. A prominent hypothesis suggests that sex and recombination are advantageous since they enhance the purging of such deleterious mutations and create individuals with a lower than average deleterious load. Deleterious mutations should co-determine the parameters that govern recombination of genomes in meiosis. Using an evolutionary computer simulation of diploid, unicellular sexual populations, we show that recessive lethal mutations can drive the evolution of chromosome architectures, in which essential genes become genetically linked into clusters. Evolved architectures exhibit structural properties and fitness similar to digitized yeast chromosomes and provide mutational purging capabilities superior to those of randomly generated or unclustered architectures. Our study demonstrates the importance of sexual cycles in the context of lethal mutations.

Introduction

Mating and meiosis are the masterpieces of an evolutionary invention thought to meet the challenges of changing environmental conditions that need to be solved by mutational inventions. Among the many hypotheses that govern the various benefits of mating and meiosis [1], two main hypotheses stand out: enhanced purging of deleterious mutations [2] and the combination of beneficial alleles into one genome [3]. It remains a matter of discussion, however, which of these advantages constitutes the main reason for the evolution of sexual recombination and, furthermore, its continuing prevalence in most eukaryotic life forms [4],[5].

Mutations take the form of DNA lesions that are caused by environmental factors, e.g. radiation, but they are also a natural byproduct of DNA replication. Genotypes that exhibit an elevated mutation rate are frequent in nature and can be induced in studies on experimental evolution. The complex interplay of factors that govern the adaptive significance of “mutator alleles” (i.e. alleles that cause higher mutation rates) has been studied in experimental and theoretical work in unicellular organisms [6][8] and during cancer progression [9],[10]. In asexual yeast populations, a selective advantage of mutator alleles has been demonstrated, serving as a prerequisite for expanding the spectrum of mutations typically not accessible in non-mutator genotypes [11]. In this study with yeast, the mutator advantage was found to be more prominent in diploid rather than haploid cells, which can be explained by the presumed dominance of beneficial mutations [11],[12] and by the recessive nature of most deleterious mutations in yeast [13]. Furthermore, the accumulation of recessive deleterious mutations in yeast may not significantly decrease the fitness of the genotype or population growth rates, as long as the diploid nuclear condition is maintained [14].

S. cerevisiae and many other yeast and fungal species seek to maintain the diploid state of the genome, if possible; after meiosis this usually happens by immediate mating of the gametes following germination. Mating occurs mostly between closely related spores, either among products of the same meiosis, or between spores from related cells according to population structure [15]. Outcrossing between unrelated strains [16] and even between closely related species of the sensu stricto yeast group does occur [17]; these events appear to be extremely rare, but they might be important for generating new persisting lineages. However, whether these rare events suffice to create a selective pressure towards maintaining a sexual cycle is doubtable.

Upon inbreeding, high rates of homozygotisation occur at various loci. This is reduced for loci linked to the MAT locus, since mating type heterozygosity is the prerequisite for a mating event. A MAT-linkage to centromeres is frequently observed in yeast and other fungi [18]. In S. cerevisiae, the genetic distance between the two loci is in the range of 18–30 cM [19], which is much smaller than expected from the physical length and caused by a region intervening these two loci that is cold for meiotic recombination [20]. In Neurospora tetrasperma MAT linkage to the centromere is enforced by crossover suppression in a long region of the chromosome, which correlates with an extensive unpaired region at pachytene [21]. Reasoning for such arrangements is provided by population genetic models that suggest a selective advantage arising from shielding of recurrent deleterious load via linkage to the MAT locus [22]. Population genetic modifier models that investigate alteration of the inbreeding frequency predict the evolution of high inbreeding rates, in particular for spores from the same tetrad (i.e. automixis), and the linkage of load loci to the MAT locus [23],[24]. These MAT linked chromosomal recombination abnormalities are believed to have initiated the evolution of sex chromosomes, which was then continued by expansion of the recombination suppressed region through the recruitment of other sex-related factors [25],[26].

Non-random distribution of meiotic recombination throughout the genomes into cold and hot regions has been reported for many species [27], but the molecular mechanisms as well as the selective forces that generate these patterns are still not fully understood.

Similarly, the distribution of genes along chromosomes appears to be non-random, and in many species a significant clustering of essential genes (“housekeeping genes”) has been reported [28],[29]. In budding yeast, a prominent genome-wide enrichment of essential genes has been observed in regions that are cold for meiotic recombination [30]. This finding is consistent with the observation of a slight enrichement of essential genes near the centromeres [31], which are known to be cold for meiotic recombination [32],[33]. Current models speculate about mechanisms of co-expression and reduction of gene expression noise as the driving force that shaped these patterns [29], [30], [34][36]. However, the selective advantage of such a scenario has not been demonstrated, and proof that single rearrangements associate with an advantage sufficient for their selection has not been provided.

An alternative mechanism that may pool essential genes into clusters with a reduced probability of disruption by frequent crossovers could be a selection based on their common denominator. This appears to be their essential nature only, as no functional correlation of essential genes within the same cluster has been observed [30].

Meiotic recombination is favorable for purging deleterious load from populations. We hypothesize that clustering of essential genes may further enhance purging efficiency of lethal load from sexual populations, since non-uniform distributions of essential genes and crossover sites change the global genetic linkage relationship of all essential genes (as compared to situations with uniform or random distributions). In the context of a scenario with more than one lethal mutation in the genome, this will influence the segregation of mutations during meiosis and subsequent mating.

In order to address this question, we computationally studied the correlation between non-random distributions of essential genes and meiotic recombination with lethal load affecting essential genes. A Monte-Carlo-simulation of breeding diploid yeast populations and chromosome architectures, termed S. digitalis, allowed us to investigate the fitness of any genome architecture upon exposure to lethal mutations. We find that several hallmarks of yeast chromosome crossing over during meiosis are consistent with natural selection imposed by recessive lethal mutations affecting essential genes (see Figure 1 for an overview of our approach and the results).

Figure 1
Conceptual overview of the methods and main results of this study.

Our simulations imply that lethal phenotypes are frequently caused by single essential gene inactivation. Alternatively, lethal phenotypes may arise from genetic interactions between only weakly deleterious mutations. We explored both possibilities using a conditional yeast mutator strain and analyzed the causes of the accumulation of haploid lethal phenotypes. By determining the global effect on germination and mating, we tested whether the associated load is being transmitted into the next round of diploid growth.

Our combined results suggest an evolutionary history for yeast where sex and meiosis fulfilled a need for efficient purging of mutational load in important/essential genes.

Results

Simulation of digital yeast genomes with S. digitalis

We sought to assay the consequences of non-random distributions of essential genes and meiotic recombination hotspots for the fitness of populations upon frequent inactivation of essential genes by lethal mutations. This analysis requires a direct comparison of the fitness of yeast strains with the same genomic content but different arrangements of the genetic elements. Conducting an experiment such that this question can be addressed in isolation from the many other possible consequences of human-designed genomic architectures is far from trivial. Therefore, we developed a computer simulation of populations of digital genomes subjected to digital life cycles of mitosis, meiosis and mating, modeled according to a simple yeast life cycle (Figure 2A). We used this simulation to study the relationship between genome architecture and the fitness of populations as well as the evolution of genome architectures upon exposure of populations to essential gene inactivating mutations (Figure 2B).

Figure 2
Yeast life cycles and mutation homeostasis.

Haploid lethal mutations are frequently observed in yeast and constitute approximately 40% of all deleterious mutations [37],[38] (see also below). The remaining fraction of deleterious mutations has been reported to exhibit a weak impact on fitness [37] and both types of mutations are shielded well in heterozygous diploids [39]. Therefore, we decided to focus on heterozygous lethal mutations, which confer a lethal phenotype either on the level of haploids or upon homozygotisation of mutations in diploids (Supplementary Figure 1A in Text S1).

S. digitalis simulates populations of diploid digital organisms with one chromosome, which consists of different building blocks: genes, intergenic elements, centromeres and mating type loci (MATa and MATα). The digital genes are either non-essential or essential. Each gene of the latter category carries a unique identifier. Genes are separated by intergenic elements (IE). IEs are either cold for crossing over ( = coldspots) or hot ( = hotspots). Each feature is represented by an element in the matrix of the population genome, and mutations only affect elements that represent essential genes (Figure 3A). Typical natural yeast chromosomes contain a few hundred genes, and so do our digital counterparts. Populations have a finite size and typically consist of a few hundred to ten thousand diploid individuals.

Figure 3
Digital genomes and the life cycle of digital populations.

Mitosis yields a copy of the original genome. It differs from the template genome by mutations, which are introduced at random and lead to the inactivation of essential genes (Figure 3B). The statistical frequency of essential gene mutations per diploid genome and mitosis is given by the genomic recessive lethal mutation rate R [40] (for example, R = 1 corresponds to an average of one essential gene inactivation per diploid genome and mitosis).

Genomic rearrangements can be simulated. They manifest themselves either as positional swapping of genes and associated intergenic elements, or as segmental inversions (Figure 3B). Genomic rearrangements occur in mitosis and always affect both homologous chromosomes.

In meiosis, the genome duplicates and the homologous chromosomes undergo meiotic recombination (crossing over). The distribution of crossover sites considers meiotic recombination hotspots and crossover interference based on a genetic distance definition (hotspot distribution). The crossover frequency can be adjusted by the shape factor of the Erlang distribution that is used to describe crossover interference (Figure 3C). The four meiotic haploid progenitor genomes constitute a tetrad.

Mutations are allowed to occur in mitosis (see Text S1, section “Supplementary Results and Discussion” for an analysis of meiotic mutations). This implementation considers one single mitotic cycle between consecutive meiotic cycles. This mimics a situation in which many consecutive rounds of mitoses occur without exponential growth. This applies to scenarios where a high loss of individuals occurs (e.g. many individuals eaten by predators or washed away into non-fertile grounds) that keeps the size of a local population more or less constant. Under circumstances where deleterious mutations are recessive and do not influence the fitness of the cells (as indicated by literature [39]), this would lead to the accumulation of mutations during the vegetative period of the life cycle. This simplified scenario should come close to a realistic description of natural S. cerevisiae that is consistent with the absence of reports of large natural cultures of S. cerevisiae (outside of human-engineered fermentation processes). Moreover, this approximation allows us to simulate large numbers of complete life cycles, which would otherwise be inaccessible due to computational limitations.

Upon germination, the haploid genomes directly engage in mating with other haploid genomes (Figure 3D). Mating can occur between genomes from the same meiosis, which is called intratetrad mating and more generally referred to as automixis or inbreeding. Mating between haploid genomes from different tetrads can also occur, and is referred to as amphimixis or outbreeding. In this article, we use the terms inbreeding and outbreeding to distinguish between the two principal types of mating partner selection in the simulation: mating inside and outside the tetrad. Outbreeding events may nevertheless bring closely related genomes together, simply due to the finite size of the simulated populations. The total fraction of inbreeding matings per round of mating can be specified. Mating optionally considers mating types, of which two exist (MATa and MATα). The MAT locus can be placed anywhere on the chromosome. In this case, the modeled chromosome can be considered to be the sex chromosome. Alternatively, the simulation can employ a virtual second chromosome that contains the MAT locus next to its centromere. In intratetrad mating, this causes a linkage of the MAT locus to the centromeric region of the investigated chromosome [41].

Diploid genomes with different gene order belong to different species. Individuals from different species are not able to mate with each other. These species represent sub-populations, which emerge in simulation scenarios with genomic rearrangements. Alternatively, different sub-populations can be specified at the beginning of the simulation, e.g. in order to compare the fitness of different genome architectures (species) in survival competition assays.

Fitness of the individuals is assessed in the diploid stage before mitotic or meiotic cell division. We furthermore assumed that mating is not prevented by a haploid lethal mutation in an essential gene (this assumption was experimentally tested; see below, section “Mating rescues genomes associated with lethal mutations”). We decided to use a simple fitness denominator for individuals: a 1 is assigned for diploid genomes that contain at least one functional copy of each essential gene, while a 0 is assigned for genomes, in which both copies of at least one essential gene are non-functional. Individuals with a fitness of 0 are removed. Hence, the only criterion underlying the loss of an individual due to mutations is the homozygotisation of a mutated essential gene. This can occur in two different ways: a new mutation inactivates the second wild type copy or a mating event brings together two chromosomes that both contain a mutated allele at the same position.

Populations were limited in size according to a defined maximum (the population size cap). Excess individuals are removed at random before the next round of mitotic or meiotic division. This simulates limited availability of nutrients. As a result, a selective pressure is introduced that has the potential of driving the evolution of species ( = different genome architectures) that are better adapted to handle lethal mutations. Supplementary Figure 1A and 1B in Text S1 provides an overview of the mechanisms of the simulation.

The simulation provides modules for different types of experiments, including mutational robustness benchmarks of populations with specific genomic architectures, selection advantage assessments with two or more isolated populations that compete for nutrients and evolution experiments of large in- and out-breeding populations that constantly undergo genomic rearrangements (see Text S1). Detailed descriptions of all simulation modules and the implementation of yeast and model chromosomes are provided in Text S1.

S. cerevisiae chromosome architecture provides enhanced mutational robustness

Using S. digitalis we first assessed the maximum mutation rate R populations with random distributions of genes and recombination hotspots can resist before becoming extinct (the mutational robustness Rmax). We compared the results with the mutational robustness obtained for the S. cerevisiae chromosome IX architecture, which deviates significantly from a random arrangement of essential genes and meiotic recombination hotspots distribution [30]. This revealed a superior mutational robustness of the yeast chromosome architecture for the entire spectrum of inbreeding fractions (Supplementary Figure 4A; Supplementary Figure 2A in Text S1). We obtained the same result when allowing mutations to occur in meiosis only, or both in mitosis and meiosis (Supplementary Figure 2B and 2C in Text S1).

Using a survival competition assay, we directly compared the persistence of populations with random chromosomes and of populations with yeast chromosome IX at different mutation rates and for different population sizes. The competition experiments revealed a clear selective advantage of the yeast chromosome IX architecture for most regions of the investigated parameter space (Figure 4B). A stalemate situation was only observed at low mutation rates R<0.01 and for extreme inbreeding fractions (i = 0 and i = 1) (Figure 4B and 4C). We performed a control experiment to demonstrate that the quantitative outcome of the survival competition assay is unaffected by the choice, in which life cycle state mutations are simulated (mitosis and/or meiosis) (Figure 2D in Text S1).

Figure 4
Competitive fitness advantage of yeast chromosomes in the presence of lethal mutations.

An analysis of the recently recorded distribution of 4,300 single crossover events in 50 meioses of yeast [42] indicated non-random distributions of crossovers and essential genes for the entire yeast genome. We found that the resulting average level of clustering is more than 2.5σ higher than the level expected for random distributions (Table 1 in Text S1). Using S. digitalis, we obtained comparative data by subjecting digitalized implementations of all chromosomes (Text S1) to a survival competition against randomly generated chromosomes. The simulation outcome attests a superior fitness to almost all of the yeast chromosomes (Figure 4D).

Taken together, our data suggest that yeast-like chromosome architectures contain evolved features consistent with selection imposed by lethal mutations.

CEN-linked and peripheral essential gene clusters provide cumulative benefits

The fitness advantage for the structure of chromosome IX relative to randomly structured chromosomes may result from essential gene clusters that are either centromere-linked or peripheral to the chromosome, or cumulatively from both. We designed synthetic chromosome architectures to discern the potential impact of these structural relationships. First, in simulations without MAT loci, the highest average Rmax were obtained for synthetic chromosomes, in which essential genes were distributed in a few large clusters (Figure 5A). Moreover, the variability of Rmax as a function of the inbreeding ratio was larger in the case of the chromosomes with less essential gene clustering. The number of clusters providing the best performance depends on the population size: the larger the population the smaller the optimal number of clusters the pool of essential genes must be distributed to (Figure 5B). For clustered architectures, the introduction of a MAT locus (which constitutes an obligatory heterozygosity) into one of the clusters increased the persistence compared to genotypes without a MAT locus (Figure 5A, inset; and Supplementary Figure 3 in Text S1). Using survival competition assays in genomes with MAT-linked clusters, we compared the fitness of genotypes with peripheral essential genes either in clusters or in random distributions. We obtained a fitness advantage of peripheral clustering for a wide range of inbreeding ratios and mutation rates (Figure 5C). Thus, MAT-centromere-linked clusters and peripheral essential gene clusters provide cumulative fitness benefits.

Figure 5
Effect of essential gene clustering on mutational robustness.

Achiasmate meiosis enhances the mutational robustness of digital genomes

The tight physical linkage of all essential genes into a single, large cluster is not a very likely configuration for natural genomes. However, achiasmate meiosis (the absence of meiotic crossovers) results in a comparable situation, since it genetically links together all essential genes on a chromosome. In the following, we will use the word “achiasmate” to denote the absence of meiotic crossing over between all essential genes present on a chromosome. Meiosis without crossovers has been reported for several species [43] and was also suggested to occur in the hemiascomycete yeast Saccharomycodes ludwigii [44],[45]. Using our survival competition assay we found that achiasmate meiosis exhibits a high mutational robustness Rmax (Supplementary Figure 3 in Text S1, genomes with one essential gene cluster and with mating types, +MAT) and provides a particularly strong fitness advantage in the entire investigated parameter space (considering the inbreeding fraction i and the mutation rate R) when a MAT was present (Figure 6A, top panel).

Figure 6
Fitness advantage of achiasmate meiosis.

Generally, no advantage of achiasmate meiosis would be expected for pure outbreeding. The advantage of achiasmate meiosis observed in our simulations in the pure outbreeding domain can be explained by the finite population size, which implies that all individuals are related to a certain degree.

Without MAT linkage to the essential gene cluster, the advantage is reduced, but significant for mutation rates R<1.5 and non-extreme inbreeding fractions (0<i<1) (Figure 6A, lower panel). Using direct competition, we found a strong advantage of achiasmate meiosis over random chromosomes for mutation rates R between 10−4 and 1, which further increases with increasing population size (Figure 6B and 6C). In achiasmate meiosis, linkage to the MAT locus either occurs physically (on the chromosome where the MAT locus is located) or via the centromeres (for all other chromosomes due to intratetrad mating). This preserves heterozygosity at autosomal centromeres (see Figure 6D). The resulting selection advantage may provide population-genetic reasoning for the secondary loss of meiotic crossing over in Saccharomycodes ludwigii.

De novo evolution of essential gene clustering in complex chromosomes

Our experiments demonstrated a fitness advantage of clustered chromosome architectures when exposed to deleterious mutations. This fitness advantage is the result of the cumulative effects arising from pre-existing essential gene clusters, but it does not allow us to deduce whether clustered genomes can evolve from unclustered or random architectures solely due to the exposure to lethal mutations. For example, alternative and potentially synergistic mechanisms are conceivable (see Discussion). In order to constitute a driving force, the presence of deleterious load would have to cause the emergence of clusters in a self-organized manner, exclusively based on the rules that govern the evolutionary process of genomes in the context of unicellular breeding populations subjected to deleterious mutations.

In our investigation of the in silico evolution of clustered genomes, we first dissected the complementary process: the maintenance of essential gene clusters in the context of chromosomal rearrangements and the linkage of the MAT locus to a gene cluster. We designed an initial genome that contained all essential genes in one large cluster and all meiotic recombination hotspots outside this cluster. Scenarios with and without MAT loci were considered in an inbreeding-only domain (full intratetrad mating), which is least favorable to successful persistence of the lineage in the situation without a MAT (see Figure 6A). For +MAT scenarios, the MAT locus was placed outside the essential gene cluster. Populations were evolved using different rearrangement rates (r). For rearrangement rates r<10−4, simulated architectures both with and without MAT loci preserved highly significant levels of essential gene clustering and anti-correlated meiotic crossover distributions over periods of at least 150,000 generations (Figure 7A and 7B, Video S1). Without MAT, high preservation of essential gene clustering was only observed in a relatively narrow range of mutation rates (0.6<R<1.4). In the presence of MAT loci, however, clustering was well maintained over a significantly broader range of mutation rates (R≥0.2) and also for higher rearrangement rates (Figure 7A). We found that the mating type locus had always relocated to a position inside the cluster by stochastic rearrangement (usually within the first 1,000 generations, n = 20 experiments) and had remained in the cluster afterwards. This experiment demonstrates that a significant level of clustering can be preserved in the presence of lethal mutations. Less well-clustered architectures that arise in the presence of destructive forces (genomic rearrangements) are quenched due to a selective pressure towards the better-performing clustered architectures, as long as the rearrangement rate is not too high.

Figure 7
Maintenance and de novo evolution of essential gene clustering.

In the next step, we investigated the de novo evolution of MAT-linked essential gene clusters in small model genomes containing five essential genes, five non-essential genes and four recombination hotspots (Figure 7C). We found that genomes evolved MAT linked essential gene clusters over a broad range of mutation rates and rearrangement rates, which is consistent with the fact that inbreeding preserves MAT-linked heterozygosity (Supplementary Figure 7D; and Supplementary Figure 4 in Text S1). Architectures with a single cluster (2+1+1+1, 3+1+1, 4+1 or 5 genes) were consistently favored over multi-cluster architectures (2+2+1 or 2+3 genes) (Figure 7C and 7D; grey rectangles indicate single-cluster architectures in Figure 7D).

In order to investigate the evolution of large yeast-like chromosome architectures we switched to domains with 50% inbreeding, since no advantage of chromosome-peripheral clustering was apparent for the extreme breeding domains at i = 0 and i = 1 (Figure 4 and Figure 5C). For this series of experiments, we implemented a species barrier in the simulation (see also first section of Results, and Text S1, section “Supplementary Results and Discussion”). Thereby, each genomic rearrangement leads to the formation of a new species. This scenario mimics reproductive isolation due to meiotically incompatible chromosomes. A new species might eventually dominate the population or become extinct depending on the reproductive success arising from the fitness (dis-)advantage of its particular genome architecture. We found that the simple life cycle of mitosis, meiosis and mating was sufficient to reproducibly evolve genomes with MAT-linked as well as non-random peripheral essential gene distributions (Figure 8A and Video S2). In order to obtain good statistics on this phenomenon, we parallelized the assay by using grid computing, which allowed us to simultaneously evolve many unrelated populations (n = 3,000 experiments). On average after 15,000 generations, high-R +MAT populations reproducibly evolved a level of clustering 2σ above the mean level encountered in random architectures. The evolution of the same level of clustering in low-R +MAT populations and in −MAT populations required a 2–3 fold longer period. Importantly, all high-R +MAT populations and even a small fraction of the other populations eventually arrived at the level of clustering of the natural yeast chromosome IX (emerging after 30,000–70,000 generations, statistics are provided in the legend of Figure 8A). Genomes with one MAT-linked cluster dominated at high mutation rates (R = 1), whereas genomes with several clusters, one of which associated with the MAT locus, typically evolved at lower mutation rates (R = 0.1).

Figure 8
Evolution of yeast-like essential gene clustering.

We must point out that the parameter space explored in the evolution of clustering constitutes a compromise enforced by limitations in computation time. The computation of all events during one generation requires approximately ten seconds of CPU time in a population of 4,000 individuals. In order to be able to perform a statistically meaningful number of experiments under different conditions, we applied relatively high rearrangement rates close to a “destructive regime”, in which any emerging cluster quickly became scrambled. This setting allowed us to simulate genomic restructuring as would quantitatively occur over long evolutionary timescales using reasonable amounts of computation time. However, up-scaling the rearrangement rate also necessitates up-scaling the mutation rate, in order to arrive at a selective pressure on par with the potential destructive force introduced by the random rearrangements. If computation time was unlimited, we would also expect a qualitatively comparable outcome for lower values of R in the context of lower rearrangement rates.

We were able to qualitatively reproduce our results with respect to the evolution of essential gene clustering in three additional series of experiments. In these experiments, we provided the simulation framework with unclustered architectures assembled from the genetic building blocks of S. cerevisiae chromosomes VI, VII and X (Supplementary Figure 5A in Text S1 and data not shown). Even in large chromosomes with chromosome VII- and X-like sizes, highly significant levels of essential gene clustering were reproducibly established. Moreover, similar results were obtained when using an externally linked mating type locus as well as when using lower rearrangement rates over longer evolution periods (r = 10−5 for 200,000 generations, Supplementary Figure 5A in Text S1).

Taken together, these in silico experiments demonstrate that deleterious mutations inactivating important genes can provide a sufficient driving force to reproducibly evolve chromosome architectures resembling their natural counterparts with respect to essential gene distributions, meiotic recombination hotspot distributions and MAT-centromere linkage. Therefore, a recurrent exposure to lethal mutations can select for genome architectures in order to account for the associated load in the context of a sexual cycle.

Competitive advantage of de novo evolved genome architectures

Any evolutionary process, when successful, should generate individuals that perform better under the conditions of their evolution than their ancestors. In order to determine the level of success of our evolutionary simulation, we performed survival competition experiments between the evolved genomes discussed above and random chromosomes or yeast chromosome IX. We observed a strong fitness advantage of +MAT genomes evolved at R = 1.0 when competing with random chromosomes and yeast chromosome IX (Figure 8B). As expected from the presence of large MAT-associated essential gene clusters in these genomes, the fitness advantage results for a wide range of mutation rates (R≥10−3) and for the entire inbreeding/outbreeding domain. The genomes of +MAT populations evolved at R = 0.1 also performed significantly better than random architectures, but only slightly better than the chromosome IX architecture, with the exception of mixed breeding ratios and high mutation rates (R = 1.0), for which chromosome IX performed better. In the statistical average, low-R +MAT populations exhibited almost the same overall performance as the chromosome IX architecture (Figure 8C).

To further expand this analysis, we also performed competitions of the chromosome X-like products of the evolution experiment shown in Supplementary Figure 5A in Text S1 with random architectures as well as with the actual S. cerevisiae chromosome X, using a chromosome description derived from [42]. The results of the competition experiments were qualitatively comparable to those obtained for chromosome IX (Supplementary Figure 5B and 5C in Text S1). The reproduction of our results in the context of chromosome X is particularly striking, since the digitalized chromosome X architecture exhibits the highest level of essential gene clustering of all sixteen yeast chromosomes (see Table 1 in Text S1) and therefore constitutes a particularly challenging opponent for the evolution products in the survival competition.

We conclude that, in the context of our reference life cycle, architectures with chromosome IX-like purging evolve in the regime characterized by the lower mutation rate. The high-R regime promotes the evolution of single large gene clusters, the extreme of which represents achiasmate meiosis.

Mating type switching influences the lethal load in populations

So far, we have investigated the correlation between lethal mutations in essential genes and the parameters that govern population fitness with respect to crossing over and population genetics via simulations of simple life cycles. There are also other processes that may influence the lethal load present in populations (see also Discussion). In particular, mating type switching followed by mating of daughter cells (termed “haplo-selfing”) with their respective mothers is a prominent feature of the life cycle of S. cerevisiae (but not of all yeasts, see Discussion). Mating type switching leads to a homozygous diploid, but only if it involves a haploid genome that is free of lethal mutations. Hence, if occurring at significant rates, haplo-selfing would be expected to decrease the lethal load in populations. However, if the mutagenic load in the population is too high, there is only a small probability of generating viable diploids by haplo-selfing. Comparing pre-loaded chromosomes with and without haplo-selfing revealed a sharp transition of the competitive advantage in favor of non-switching populations for a load higher than two lethal mutations per diploid (Supplementary Figure 6 in Text S1). In this regime, already a small percentage of diploidisation via haplo-selfing (2%) constituted a strong disadvantage.

To assay the impact of haplo-selfing on the fitness of different chromosome configurations, we performed several analyses. First, we compared the mutational robustness (Rmax) of chromosome IX and of random chromosomes for different levels of haplo-selfing. A high haplo-selfing rate of 50% leads to a significant increase in the mutational robustness Rmax, both for random architectures and for chromosome IX. At the lower rate of 10% haplo-selfing, the advantage of the chromosome IX architecture remained, but the mutational robustness decreased as compared to the situation without haplo-selfing (see Supplementary Figure 2A and 2E in Text S1). We further performed competitive advantage experiments of chromosome IX vs. random chromosomes at 10% haplo-selfing and for mutation rates between 10−3 and Rmax. In the absence of a mutagenic pre-load, we noticed the emergence of a phase transition in parameter space at high mutation rates, indicating a region that is dominated by random architectures (Figure 9). However, even in this extreme scenario the chromosome IX architectures, on average, still performed better than the random architectures (57% competition wins of chromosome IX vs. 43% competition wins of random architectures).

Figure 9
The effect of mating type switching on population fitness.

Meiotic crossover rates in S. cerevisiae are optimal

Using S. digitalis, we determined the influence of the meiotic crossover rate of chromosomes on fitness and on the ability to purge mutational load. In yeasts, crossover rates vary considerably, from 0 (achiasmate meiosis) up to approximately 20–40 crossovers per chromosome in S. pombe. The genomic mean for all S. cerevisiae chromosomes is 5.6 crossovers per meiosis (derived from the genetic map, www.yeastgenome.org) [46]. This value was confirmed by the direct assessment of crossover frequency and distribution [42]. The chromosome-specific number of crossovers scales linearly with the number of genes (R2 = 0.89), in a range of 2.5–9 crossovers for individual chromosomes (Supplementary Figure 7 in Text S1). We used random genomes of different sizes (250–1,500 genes) to assess the mutational robustness Rmax as a function of crossover frequency and inbreeding fraction. This revealed an increase of Rmax with increasing crossover rates, reaching saturation levels (95–99.5%) in the range of 4.5–8 crossovers. The observed variability of Rmax as a function of the inbreeding fraction was minimal in the 95–99.5% saturation interval (Figure 10A). A slight dependency on chromosome length was apparent (Figure 10A, inset). Direct competition of chromosome IX populations subjected to the natural crossover rate with chromosome IX populations at modified crossover rates demonstrated that crossing over rates higher or lower than the naturally observed average lead to a decrease in the fitness advantage (Figure 10B; see Supplementary Figure 8 in Text S1 for a plot of the average performance). Moreover, when assessing competition experiments of chromosome IX versus random architectures as a function of the crossover rate, chromosome IX performed best in a regime of yeast-like crossing over rates (Figure 10C; see Supplementary Figure 8 in Text S1 for a plot of the average performance). This suggests that the natural rates of meiotic crossovers in S. cerevisiae are adapted to handle deleterious load.

Figure 10
Natural crossing over rates for yeast chromosomes are optimal.

Lethal mutations are frequently associated with single loci

Haploid lethal phenotypes may be caused by mutational inactivation of one essential gene, or they may arise as a consequence of cumulative effects of non-lethal mutations in essential and non-essential genes. Dissecting synthetic lethal relationships demonstrated a 0.8–4% chance of lethality when two non-essential genes are deleted [47]; a simple extrapolation predicts a 50% chance for a lethal phenotype upon inactivation of approximately 7–14 non-essential genes, assuming scalability (and ignoring the possibility of non-linear network properties, such as positive epistasis [48]). In this case, however, most of the cells would have died before reaching such a high load, due to inactivation of one of the 19% essential genes. This rather empirical analysis might indicate that many haploid lethal phenotypes are caused by inactivation of a single essential gene, as we hypothesized for the purpose of our investigation.

In order to test this hypothesis directly, we generated a diploid strain containing MSH2 under control of the weak and fully repressible GalS promoter in order to perform mutation accumulation experiments. Deletion of the mismatch repair gene MSH2 leads to greatly elevated levels of point mutations [49],[50]. Additionally, reduced sequence specificity for homologous recombination was observed [51],[52], leading to increased levels of recombination between similar sequences at separate loci (ectopic recombination). Mismatch repair deficient strains accumulate high levels of lethal mutations, which are however not associated with an increase in gross chromosomal rearrangements [53].

Growth of this conditional mutator strain on glucose-containing medium led to depletion of Msh2 from the cells (Figure 11A and 11B) and to the accumulation of mutant phenotypes with reduced viability. In order to restrict the accumulation of mutations to vegetative growth, we shifted the cells to galactose-containing medium to induce MSH2 expression prior to sporulation (Figure 11A), which also prevents aberrant post-meiotic segregation events and ectopic recombination associated with the MSH2 deletion [54]. When grown exclusively on galactose-containing medium, the GalS-MSH2 strain exhibited wild type spore viability (Figure 11C). Upon mutation accumulation for approximately 30–36 generations (three growth periods of one day each), tetrad analysis (n = 400) revealed little 3-spore or 1-spore viability (8% and 15.5%). The majority of tetrads with unviable spores contained two viable spores (36%), which could be caused by single locus events leading to haploid lethality. Alternatively, some 2-spore viability may have resulted from meiosis I non-disjunction. We tested this option by measuring the linkage of the lethal load in 2-spore viable asci to the heterozygous leu2/LEU2 locus, which itself is centromere-linked (5 cM), and found that the lethal load exhibited on average only partial linkage to leu2 (27 cM). Since the load locus is different in each analyzed tetrad, only in approximately 25% of all cases crossing over between the centromere/leu2 locus is prevented (see Text S1, section “Supplementary Results and Discussion”), either due to tight centromere linkage of the load or as the consequence of homologous non-disjunction in meiosis I. Therefore the prominent fraction of tetrads with two viable spores is likely to be caused by freely segregating single mutagenic events affecting an essential function/gene. Importantly, the frequency of tetrads with only one dead spore was low, indicating low cumulative lethal effects of non-lethal mutations recombined into a haploid genome during meiosis. Taken together, these data suggest that losses of genomes associated with random mutagenic events are frequently associated with single events leading to a lethal haploid phenotype.

Figure 11
Mutation accumulation and genetic analysis of lethality and mating.

Mating rescues genomes associated with lethal mutations

In this scenario, any linked mutation providing an advantage is lost as soon as the lethal mutation becomes exposed, e.g. by haploid growth following meiosis or homozygotisation. However, the genome with the lethal mutation may be preserved via mating with a spore containing the wild type allele. In order to test whether haploid lethal mutations have a high or a low chance to render spores unable to mate, we investigated the rates of diploid colony formation of single dyads using fluorescence activated cell sorting (FACS) after different mutation accumulation periods (Supplementary Figure 9 in Text S1). The observed frequency of diploid colonies did not change significantly as a function of accumulated mutations, when compared to the wild type. If spores associated with lethal mutations were frequently unable to mate – either due to the lethal mutation itself or due to co-accumulated non-lethal mutations – a greater than two-fold decrease of diploid colonies during the course of the experiment would have been expected (Figure 11C). Consistently, we found that only a very minor fraction of viable spores were impaired in mating and that dead spores would still germinate and often form microcolonies (see Text S1, section “Supplementary Results and Discussion”; and Supplementary Figure 10 in Text S1 for a histogram of the colony sizes). This latter result is also consistent with our observation that the majority of lethal phenotypes are not caused by meiosis I non-disjunction, as spores that lack entire chromosomes usually fail to germinate. Taken together, our results show that the majority of randomly occurring lethal mutations did not prevent the spores from mating.

Discussion

We investigated the influence of deleterious mutations on the evolution of genome architectures. In breeding unicellular diploid organisms subjected to high mutation rates, the frequent inactivation of important genes selects for non-random distributions of important/essential genes and meiotic recombination hotspots. In simulated experiments architectures evolve, which bear a striking resemblance to the architectures of natural yeast chromosomes and provide a competitive advantage over a wide range of mutation rates.

Purging of deleterious mutations

The selective advantage of clustered genomes arises from multiple effects that cumulatively improve the fitness of such genomes. Initially, the average mutational load (An external file that holds a picture, illustration, etc.
Object name is pgen.1000533.e003.jpg) in a simulated population subjected to a mutation rate R increases until an architecture-dependent equilibrium is reached. In this equilibrium, the influx of new stochastic mutations is equal to the outflux associated with loss of individuals from the population (Figure 2B). Upon elimination of an individual, all mutations associated with its genome are also removed from the population (Supplementary Figure 1A in Text S1). Within the simulation framework, the loss of individuals occurs via two factors. First, the random removal of excess genomes due to the population size cap is entirely neutral, since it affects all evolved sub-populations with the same probability. Second, and most importantly, genomes are lost due to homozygotisation of a mutant locus. The probability of a homozygotisation via a new mutation during the vegetative division is proportional to the mutational load present in a genome, irrespective of the genome architecture. A higher mutational load in a population therefore lowers its fitness in mitosis due to the increased sensitivity to new mutations, even if the heterozygous load is entirely neutral. Therefore, the only process whose outcome can be improved is meiosis and the loss of individuals due to homozygotisation after mating. Since homozygotisation of any single recessive lethal mutation removes the whole genome from the population, including the associated mutations, the effect of clustering can be explained generally by a reduction of the total number of individuals that are lost after mating. This maximization of mutation purging is caused by the evolutionary optimization of the genome in the context of a sexual lifestyle. Supplementary Figure 11 in Text S1 illustrates a simple scenario.

Clustering increases the level of genetic load that can be maintained in the genome. In order to obtain a positive overall effect, clustering needs to compensate for increased mitotic losses, which in simulations of random chromosome architectures constitute approximately 20% of all homozygotisation losses during one life cycle. In those simulation scenarios, in which a large EG cluster evolved (R = 1.0), mitotic losses can reach the same magnitude as meiotic losses (Supplementary Figure 12 in Text S1).

In conclusion, the advantage of clustered genomes must arise from an increase in reproductive fitness in mitosis and meiosis. This results from an optimized balancing of all factors that influence the frequency, with which homozygotisation of a lethal load locus occurs (Supplementary Figure 1B in Text S1 and Supplementary Figure 11 in Text S1). In mitosis, homozygotisation of lethal mutations is dependent on new mutations and the global load in the population, while in meiosis, homozygotisation results after mating. This is influenced by crossover distribution and frequencies, the breeding behavior and the genetic linkage relationship between crossover sites and essential gene loci.

In several experiments, we applied mutation rates higher than the average deleterious mutation rate reported for some S. cerevisiae strains [37],[55],[56]. However, as noted in the description of the simulation (see Results, section “Simulation of digital yeast genomes with S. digitalis”), we did not assume an exponential growth of our populations, but rather implemented a scenario where species compete for a limited pool of nutrients. In this scenario our implementation of only one round of mitosis between consecutive meioses mimics a scenario of many mitoses without population growth. Although this may not properly describe the growth of a population in a local niche for a short period of time, it certainly does recapitulate longer evolutionary periods that include many consecutive sexual cycles. It is reasonable to assume that natural yeast populations undergo more mitoses than meioses. Hence, if the mutation rate is to be compared to the natural mutation rate, it must be divided by the average number of consecutive mitoses. This number, however, is currently not known.

Crossing over suppression near centromeres and the hotspot–crossover relation

Crossover suppression near centromeres may also be caused by the interference of pericentromeric crossovers with proper meiotic chromosome segregation [57]. Alternatively, it has been proposed that cold centromeres may be caused by a requirement to protect centromeric repeats [58]. These considerations relate to a general issue in evolutionary biology: frequently, several independent or interacting mechanisms exist or are at least conceivable to explain an observation. As a result, it is often difficult to precisely define the scenario in which one or the other mechanism is dominant and how different mechanisms interact with each other. The situation is further complicated, since there are usually exceptions to each explanation (e.g. species, in which certain aspects are different): yeast does not exhibit centromeric repeats; there are species, in which crossovers occur preferentially in centromere-proximal regions [59], etc. The fact that there are molecular mechanisms that provide support for different scenarios (crossovers close to or further away from centromeres) makes it difficult to deduce the causal connection.

Exploring whether a specific mechanism is singularly able to provide a valid explanation constitutes one strategy to tackling this issue. In the case of S. cerevisiae, our evolutionary scenario is able to recapitulate the evolution of crossover suppression and essential gene enrichment in pericentromeric regions. Our simulation provides evidence that lethal mutations and chromosome evolution interact. But, of course, there is no record for the true historical events that enforced this constellation. The complete answer could be given by exploring the (derived) genomes of all ancestors of S. cerevisiae along with the evolution of the molecular mechanisms that govern centromeric crossover protection (which is still subject to investigation).

While we took advantage of recent data from Mancera et al. [42] in many experiments involving the digitalization of natural yeast chromosomes, our digital implementation of chromosome IX was derived using the hotspot mapping data from Gerton et al. [32]. In the meantime, additional hotspot data sets have been published [60],[61]. Using data sets about double strand breaks to predict the distribution of crossovers is accompanied by the limitation that DSB frequencies do not translate linearly into crossover frequencies. In this sense the Gerton et al. data set (which was the only data set available at time we began our analysis) was very helpful [32], since it provided a correct description of cold centromeres, as confirmed by the yeast genetic map. Two more recent studies [60],[61] detected more DSBs near centromeres, which, however, do not convert into crossovers (www.yeastgenome.org, see Text S1, section “Supplementary Results and Discussion” for a quantitative assessment of the cM-to-kb relationship in pericentromeric regions). These studies do not deviate so much from the Gerton et al. study in the rest of the genome (except for the subtelomeric regions, which are not so relevant in our context).

The mutator scenario for genome evolution

Natural isolates of S. cerevisiae were reported to exhibit large diversity in terms of mutagenic load, yielding a significant fraction of isolates with low to extremely low spore viability. Some proportion of this load, which must have accumulated during mitotic growth and preserved during inbreeding [62],[63], may have been caused by mutator phenotypes. Widespread occurrence of natural variation that can give rise to mutator phenotypes has been reported [64],[65]; this or a similar type of variation may be the reason for the formation of natural yeast strains with highly unstable karyotypes [66]. These may be caused by impaired recombinational repair, as indicated by a certain dependency on Rad52 [67]. Interestingly, these strains can give rise to meiotic offspring with stable karyotypes.

Based on these considerations we speculate that genomic rearrangements, which are associated with the formation of new species or lineages, are frequently also associated with high mutation rates that occasionally – and in particular during the periods that shape the genome – exert a selective pressure by means of high levels of lethal mutations.

The yeast evolutionary history governs several hundred million years and includes many species with (at least nowadays) predominantly diploid life cycles [19],[68],[69]. Although the average frequency of meioses is unknown (from the general perspective as well as for individual species), a more than sufficient number of sexual cycles and genomic rearrangements must have taken place to allow for the maintenance and selection for particular genome architectures.

Mating type switching and loss of heterozygosity (LOH)

In yeast, mating is a highly favored process that occurs whenever two cells of opposite mating type meet − in dense populations or on the level of the spores of a tetrad [31],[70]. Even considering that S. cerevisiae sometimes aborts the formation of one to three spores during sporulation (due to limited availability of nutrients), the overall formation of spores with a mating partner available from within the same tetrad is well above 80% for a broad range of conditions [31]. This circumstance as well as the possibility of mating of spores from different tetrads indicates that mating type switching is most likely not the dominant way of diploidisation in S. cerevisiae. Thus, it appears safe to assume that the relative effects we observed at a level of 10% haplo-selfing represents an overestimation of the actual situation, rather than an underestimation.

Mating type switching was one of the key inventions of lifestyle variation that emerged around the time point of the whole genome duplication [68],[71]. One may wonder about the reasons for this evolutionary invention in the first place, and what causes its recurrent secondary loss (mating type switching deficient S. cerevisiae may constitute up to 10% of the strains isolated from natural wine fermentation, [72]). Lifestyles seem to evolve towards a preference for diploid stages [73], in which heterozygosity can be maintained. An associated need for efficient purging of load may have influenced the evolution of mating type switching. Occasionally, when mutation rates become too high or meiotic cycles too infrequent, a resulting high lethal load may also be able to select against mating type switching. Diploidy in the context of lethal load can enforce the evolution of very high levels of intratetrad mating in unicellular eukaryotes [23], as observed in the non-switching pre-WGD duplication yeast species Saccharomyces kluyveri [74] and Saccharomycodes ludwigii [45],[75]. These considerations together do not exclude additional or other roles for mating type switching and intratetrad mating, but they suggest that lethal mutations and mutagenic load may frequently accompany diploid life cycles in unicellular organisms.

Additional mechanisms exist that influence the lethal load in diploid populations. Loss of heterozygosity associated with mitosis acts in a position-specific manner with increased frequency further away from the centromere. It could therefore provide an additional reason for essential gene enrichment in pericentromeric regions. However, its frequency is low (approximately 0.5 to 10 per 10,000 cell divisions in young cells and 50 to 500 in old mother cells [76]) and it is therefore unlikely to significantly influence the global lethal load of the populations.

“Survival of the flattest” and how to improve further

In a race for beneficial mutations upon exposure to new conditions, essential genes would effectively reduce genetic drift, if their inactivation caused a significant fitness reduction in the diploid organism. Consequently, the chance of acquiring new mutations not immediately accessible to the original genome would decrease, e.g. reducing the frequency of beneficial mutations that are accompanied by a mutation that causes the loss of an essential function.

The occurrence of deleterious mutations is predicted to select for the evolution of properties that increase robustness, even if the evolved genomes have a lower maximum fitness in the mutation-free environment. This is compensated by the higher mean fitness of the variants present in a mutant population, known as “survival of the flattest” [77]. Support is provided by studies of viruses and bacteria, but also by studies using digital organisms [78]. An important body of literature is summarized in Wilke and Adami (2003) [79]).

In yeast, several mechanisms exist that account for buffering mutational load. One is global buffering or positive epistasis of the fitness reduction in combinations of non-essential gene deletions [48]. Essential genes exhibit less expression noise than non-essential genes [80],[81]. Batada and Hurst [36] have proposed that the evolution of essential gene clustering was driven by their accumulation into chromosomal regions of low average nucleosome occupancy (open chromatin), which are domains with lower expression noise and which coincide with the domains of low meiotic recombination [82]. Although this idea is intriguing, no support has been provided that this scenario results in a fitness advantage sufficient to select for the relocation of an essential gene into a cluster. S. cerevisiae grows predominantly as diploid. Since the individual intrinsic noise from one copy of a gene is uncorrelated to the noise from the other copy, a lower total noise level is present in diploids as compared to haploids [83]. Selection of low noise for essential genes would thus be less effective in diploids than in haploids. Only about 9% of heterozygous deletion strains of essential genes exhibit haplo-insufficiency in S. cerevisiae [84], indicating that low noise may be particularly important in a diploid situation, where one copy of an essential gene is inactivated due to a mutation. This would minimize noise in the context of an overall reduced protein level. This result would suggest that a significant interaction may exist between the low noise model and purging of mutations from diploids, which could act synergistically towards improving the clustering of essential genes.

Proliferation of tumor cells depends on the inactivation of tumor suppressor genes by subsequent multiple mutations. Due to early-acquired mutations in DNA mismatch repair and other pathways required for genetic stability [10], [85][87], mutator phenotypes have the potential of accelerating the progression of cancer development by enhancement of the variability upon which Darwinian selection can act [9],[10],[88]. In this scenario, evolved robustness towards haploid lethal load is an important factor that has implications for the understanding of genetic instability in cancer development.

Conclusions

Purging of deleterious load depends on the tendency to accumulate load and on the presence of alleles that increase the rate at which mutations occur (i.e. mutator alleles). The robustness inherent to the genome architecture of yeast therefore indicates that high mutation rates and genetic load have played an important role during evolution, when the ability to deal with deleterious load co-evolved with better suited genome architectures. Altogether there is increasing evidence that deleterious load is common to evolving yeast populations and that many aspects of the cellular physiology evolved to allow survival as fit but “flat” species.

Methods

Yeast mutator experiment

A diploid strain carrying chromosomal MSH2 under control of the inducible GalS promoter was constructed [89] in the well-sporulating SK1 genetic background [90]. The cells were constantly maintained under GalS inducing conditions (YP-galactose/raffinose (YP-Gal), see also Text S1, section “Supplementary Methods”) and exhibited wild type spore viability. In order to allow random mutations to occur, the GalS promoter was repressed using glucose while cells were grown for 24, 48 and 72 hours (24 hours≈10–12 generations) using serial dilution. At each time point, an aliquot of the cells (5·107 cells) was plated on YP-Gal for 16 hours. The cells were then washed off, plated on a sporulation plate (1% KAc, 0.02% raffinose, 0.02% galactose) and incubated for 40 hours at room temperature. Ascus formation occurred in all cases with frequencies >99%. After disrupting the asci, FACS sorting was used to spot single spores and dyads on large YP-Gal plates (1536 spores or 384 dyads per plate). Sorted spores and dyads were analyzed for colony formation (viability) and mating type (MATa, MATα and no mating type = diploid cells) using mating type tester strains and a halo assay (Text S1, section “Supplementary Methods;” and Supplementary Figure 9 in Text S1). The viability of the spores from 400 different tetrads was analyzed by tetrad dissection.

Simulation framework of yeast genome evolution—S. digitalis

The source code of the simulation S. digitalis is provided as Protocol S1. A detailed description of the simulation is included in Text S1, section “The Computer Simulation S. digitalis;” and in Table 2 in Text S1.

Supporting Information

Text S1

The computer simulation S. digitalis; supplementary results and discussion; supplementary materials and methods; supplementary figures and tables; S. digitalis simulation settings.

(1.26 MB PDF)

Protocol S1

S. digitalis simulation. Matlab source code. Version 1.79 (2005–2009), Philipp J. Keller, EMBL Heidelberg.

(0.05 MB ZIP)

Video S1

Maintenance of EG clustering at low and at high mutation rates. Maintenance of essential gene clustering in evolving inbreeding populations for two of the data points in Figure 7A in Main Text. The right panel corresponds to data point #1, while the one to the left corresponds to data point #2. The graphs at the top show the genomic element densities for the entire population. Chromosomes are vertically aligned. The color-coding reports the differences in density of EGs and recombination hotspots (sliding window analyses of individual genomes, window size is 20 elements). Histograms of the sliding window analyses are shown at the bottom. Initially, all EGs are located on one side of the chromosomes, while recombination hotspots form a cluster in the middle of the non-essential genes (at the other end of the chromosome). At high mutation rates, the EG clustering is maintained (left, movie shows a period of 100,000 generations). At low mutation rates, EG clustering is not maintained and the EGs become distributed in random patterns (right). Both simulations used identical values for all parameters except for R.

(1.26 MB MOV)

Video S2

Evolution of EG clustering. Visualization of the evolution of clustered genome architectures as a function of time in a population representative for the high-R +MAT evolution experiment shown in Figure 8A in Main Text. The top left panel shows a density difference sliding window plot of all genomes (red = only essential genes, blue = only hotspots, green = equal densities of essential genes and hotspots). The bottom two panels show essential gene and hotspot densities in the entire population. The average clustering score in the population (white, SD in red) is indicated in the top right panel (dashed white line = level of clustering in random architectures [107±17]). The simulation starts with a maximally unclustered genome architecture. The inbreeding percentage is 50%. Movie playback speed: 6,000 generations per second (400 generations per frame).

(7.17 MB MOV)

Acknowledgments

We thank Sarah Otto, Lars Juhl Jensen, Michael Hood, Darren Gilmour, and our unknown reviewers for valuable comments and constructive discussions; Nicola Hastings and Audun Lier for helpful comments on the manuscript. We very much appreciate the generous support by Manfred Alef, Urban Liebel, Marc Hemberger, and Michael Wahlers in using the computer clusters at EMBL and at the Karlsruhe Institute for Technology. We thank Andrew Riddell and Alexis Perez Gonzalez for help with flow cytometry. Franklin Stahl is kindly acknowledged for advice on modeling crossover interference in yeast and Deepankar Pal for contributions to early experiments. We are grateful to Ernst Stelzer for supporting PJK. Eugenio Mancera, Wolfgang Huber, and Lars Steinmetz are kindly acknowledged for sharing data prior to publication.

Footnotes

The authors have declared that no competing interests exist.

Funding of the project occurred entirely through internal resources of EMBL. PJK is supported by a predoctoral fellowship of the EMBL International PhD Programme and by the German National Academic Foundation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

References

1. Kondrashov AS. Classification of hypotheses on the advantage of amphimixis. J Hered. 1993;84:372–387. [PubMed]
2. Muller HJ. Some Genetic Aspects of Sex. American Naturalist. 1932;66:118–138.
3. Fisher RA. The Genetical Theory of Natural Selection. Oxford, UK: Oxford University Press; 1930.
4. Zeyl CW, Otto SP. A short history of recombination in yeast. Trends Ecol Evol. 2007;22:223–225. [PubMed]
5. Maynard Smith J, Szathmary E. The major transitions in eovlution. Oxford, UK: Oxford University Press; 1995.
6. Metzgar D, Wills C. Evidence for the adaptive evolution of mutation rates. Cell. 2000;101:581–584. [PubMed]
7. Sniegowski PD, Gerrish PJ, Lenski RE. Evolution of high mutation rates in experimental populations of E. coli. Nature. 1997;387:703–705. [PubMed]
8. Taddei F, Radman M, MaynardSmith J, Toupance B, Gouyon PH, et al. Role of mutator alleles in adaptive evolution. Nature. 1997;387:700–702. [PubMed]
9. Beckman Ra, Loeb La. Efficiency of carcinogenesis with and without a mutator mutation. Proc Natl Acad Sci USA a. 2006;103:14140–14145. [PMC free article] [PubMed]
10. Nowak MA, Michor F, Komarova NL, Iwasa Y. Evolutionary dynamics of tumor suppressor gene inactivation. Proc Natl Acad Sci USA. 2004;101:10635–10638. [PMC free article] [PubMed]
11. Thompson DA, Desai MM, Murray AW. Ploidy controls the success of mutators and nature of mutations during budding yeast evolution. Curr Biol. 2006;16:1581–1590. [PubMed]
12. Kondrashov AS, Crow JF. Haploidy or diploidy: which is better? Nature. 1991;351:314–315. [PubMed]
13. Papp B, Pal C, Hurst LD. Dosage sensitivity and the evolution of gene families in yeast. Nature. 2003;424:194–197. [PubMed]
14. Sliwa P, Kluz J, Korona R. Mutational load and the transition between diploidy and haploidy inexperimental populations of the yeast Saccharomyces cerevisiae. Genetica. 2004;121:285–293. [PubMed]
15. Aa E, Townsend JP, Adams RI, Nielsen KM, Taylor JW. Population structure and gene evolution in Saccharomyces cerevisiae. FEMS Yeast Res. 2006;6:702–715. [PubMed]
16. Ruderfer DM, Pratt SC, Seidel HS, Kruglyak L. Population genomic analysis of outcrossing and recombination in yeast. Nature Genet. 2006;38:1077–1081. [PubMed]
17. Wei W, McCusker JH, Hyman RW, Jones T, Ning Y, et al. Genome sequencing and comparative analysis of Saccharomyces cerevisiae strain YJM789. Proc Natl Acad Sci USA. 2007;104:12825–12830. [PMC free article] [PubMed]
18. Zakharov IA. Intratetrad mating and its genetic and evolutionary consequences. Genetika. 2005;41:508–519. [PubMed]
19. Knop M. Evolution of the hemiascomycete yeasts: on life styles and the importance of inbreeding. BioEssays. 2006;28:696–708. [PubMed]
20. Baudat F, Nicolas A. Clustering of meiotic double-strand breaks on yeast chromosome III. Proc Natl Acad Sci USA. 1997;94:5213–5218. [PMC free article] [PubMed]
21. Gallegos A, Jacobson DJ, Raju NB, Skupski MP, Natvig DO. Suppressed recombination and a pairing anomaly on the mating-type chromosome of Neurospora tetrasperma. Genetics. 2000;154:623–633. [PMC free article] [PubMed]
22. Hood ME, Antonovics J. Mating within the meiotic tetrad and the maintenance of genomic heterozygosity. Genetics. 2004;166:1751–1759. [PMC free article] [PubMed]
23. Johnson LJ, Antonovics J, Hood ME. The evolution of intratetrad mating rates. Evolution. 2005;59:2525–2532. [PubMed]
24. Antonovics J, Abrams JY. Intratetrad mating and the evolution of linkage relationships. Evolution. 2004;58:702–709. [PubMed]
25. Ohno S. Sex chromosomes and sex-linked genes. New York, NY: Springer-Verlag; 1967.
26. Rice WR. The Accumulation of Sexually Antagonistic Genes as a Selective Agent Promoting the Evolution of Reduced Recombination between Primitive Sex-Chromosomes. Evolution. 1987;41:911–914.
27. Petes TD. Meiotic recombination hot spots and cold spots. Nature Rev Genet. 2001;2:360–369. [PubMed]
28. Hurst LD, Pal C, Lercher MJ. The evolutionary dynamics of eukaryotic gene order. Nature Rev Genet. 2004;5:299–310. [PubMed]
29. Lercher MJ, Urrutia AO, Hurst LD. Clustering of housekeeping genes provides a unified model of gene order in the human genome. Nature Genet. 2002;31:180–183. [PubMed]
30. Pal C, Hurst LD. Evidence for co-evolution of gene order and recombination rate. Nature Genet. 2003;33:392–395. [PubMed]
31. Taxis C, Keller P, Kavagiou Z, Jensen LJ, Colombelli J, et al. Spore number control and breeding in Saccharomyces cerevisiae: a key role for a self-organizing system. J Cell Biol. 2005;171:627–640. [PMC free article] [PubMed]
32. Gerton JL, DeRisi J, Shroff R, Lichten M, Brown PO, et al. Inaugural article: global mapping of meiotic recombination hotspots and coldspots in the yeast Saccharomyces cerevisiae. Proc Natl Acad Sci USA. 2000;97:11383–11390. [PMC free article] [PubMed]
33. Lambie EJ, Roeder GS. A Yeast Centromere Acts in Cis to Inhibit Meiotic Gene Conversion of Adjacent Sequences. Cell. 1988;52:863–873. [PubMed]
34. Lercher MJ, Hurst LD. Co-expressed yeast genes cluster over a long range but are not regularly spaced. J Mol Biol. 2006;359:825–831. [PubMed]
35. Poyatos JF, Hurst LD. Is optimal gene order impossible? Trends Genet. 2006;22:420–423. [PubMed]
36. Batada NN, Hurst LD. Evolution of chromosome organization driven by selection for reduced gene expression noise. Nature Genet. 2007;39:945–949. [PubMed]
37. Wloch DM, Szafraniec K, Borts RH, Korona R. Direct estimate of the mutation rate and the distribution of fitness effects in the yeast Saccharomyces cerevisiae. Genetics. 2001;159:441–452. [PMC free article] [PubMed]
38. Eyre-Walker A, Keightley PD. The distribution of fitness effects of new mutations. Nature Rev Genet. 2007;8:610–618. [PubMed]
39. Szafraniec K, Wloch DM, Sliwa P, Borts RH, Korona R. Small fitness effects and weak genetic interactions between deleterious mutations in heterozygous loci of the yeast Saccharomyces cerevisiae. Genet Res. 2003;82:19–31. [PubMed]
40. Kondrashov AS. Sex and U. Trends Genet. 2001;17:75–77. [PubMed]
41. Zakharov IA. Intratetrad mating and its genetic and evolutionary consequences. Russian J Genet. 2005;41:402–411.
42. Mancera E, Bourgon R, Brozzi A, Huber W, Steinmetz LM. High-resolution mapping of meiotic crossovers and non-crossovers in yeast. Nature. 2008;454:479–U471. [PMC free article] [PubMed]
43. Zickler D, Kleckner N. Meiotic chromosomes: integrating structure and function. Ann Rev Genet. 1999;33:603–754. [PubMed]
44. Yamazaki T, Ohara Y, Oshima Y. Rare occurrence of the tetratype tetrads in Saccharomycodes ludwigii. J Bacteriol. 1976;125:461–466. [PMC free article] [PubMed]
45. Lindegren CC. Yeast Genetics: Life Cycles, Cytology, Hybridization, Vitamin Synthesis, and Adaptive Enzymes. Microbiol Mol Biol Rev. 1945;9:111–170. [PMC free article] [PubMed]
46. Stahl FW, Foss HM, Young LS, Borts RH, Abdullah MFF, et al. Does crossover interference count in Saccharomyces cerevisiae? Genetics. 2004;168:35–48. [PMC free article] [PubMed]
47. Tong aHY, Lesage G, Bader GD, Ding HM, Xu H, et al. Global mapping of the yeast genetic interaction network. Science. 2004;303:808–813. [PubMed]
48. Jasnos L, Korona R. Epistatic buffering of fitness loss in yeast double deletion strains. Nature Genet. 2007;39:550–554. [PubMed]
49. Alani E. The Saccharomyces cerevisiae Msh2 and Msh6 proteins form a complex that specifically binds to duplex oligonucleotides containing mismatched DNA base pairs. Mol Cell Biol. 1996;16:5604–5615. [PMC free article] [PubMed]
50. Huang ME, Rio AG, Galibert MD, Galibert F. Pol32, a subunit of Saccharomyces cerevisiae DNA polymerase delta, suppresses genomic deletions and is involved in the mutagenic bypass pathway. Genetics. 2002;160:1409–1422. [PMC free article] [PubMed]
51. Harfe BD, Jinks-Robertson S. DNA mismatch repair and genetic instability. Ann Rev Genet. 2000;34:359–399. [PubMed]
52. Selva EM, New L, Crouse GF, Lahue RS. Mismatch Correction Acts as a Barrier to Homeologous Recombination in Saccharomyces cerevisiae. Genetics. 1995;139:1175–1188. [PMC free article] [PubMed]
53. Heck Ja, Gresham D, Botstein D, Alani E. Accumulation of recessive lethal mutations in Saccharomyces cerevisiae mlh1 mismatch repair mutants is not associated with gross chromosomal rearrangements. Genetics. 2006;174:519–523. [PMC free article] [PubMed]
54. Reenan RaG, Kolodner RD. Characterization of Insertion Mutations in the Saccharomyces cerevisiae Msh1 and Msh2 Genes - Evidence for Separate Mitochondrial and Nuclear Functions. Genetics. 1992;132:975–985. [PMC free article] [PubMed]
55. Hill Ja, Otto SP. The role of pleiotropy in the maintenance of sex in yeast. Genetics. 2007;175:1419–1427. [PMC free article] [PubMed]
56. Joseph SB, Hall DW. Spontaneous mutations in diploid Saccharomyces cerevisiae: more beneficial than expected. Genetics. 2004;168:1817–1825. [PMC free article] [PubMed]
57. Brar Ga, Hochwagen A, Ee LS, Amon A. The Multiple Roles of Cohesin in Meiotic Chromosome Morphogenesis and Pairing. Mol Biol Cell. 2009;20:1030–1047. [PMC free article] [PubMed]
58. Charlesworth B, Langley CH, Stephan W. The Evolution of Restricted Recombination and the Accumulation of Repeated DNA-Sequences. Genetics. 1986;112:947–962. [PMC free article] [PubMed]
59. Guo XM, Allen SK. Complete interference and nonrandom distribution of meiotic crossover in a mollusc, Mulinia lateralis (Say). Biolog Bulletin. 1996;191:145–148. [PubMed]
60. Blitzblau HG, Bell GW, Rodriguez J, Bell SP, Hochwagen A. Mapping of meiotic single-stranded DNA reveals double-strand-break hotspots near centromeres and telomeres. Curr Biol. 2007;17:2003–2012. [PubMed]
61. Buhler C, Borde V, Lichten M. Mapping meiotic single-strand DNA reveals a new landscape of DNA double-strand breaks in Saccharomyces cerevisiae. PLoS Biol. 2007;5:2797–2808. doi:10.1371/journal.pbio.0050324. [PMC free article] [PubMed]
62. Johnston JR, Baccari C, Mortimer RK. Genotypic characterization of strains of commercial wine yeasts by tetrad analysis. Res Microbiol. 2000;151:583–590. [PubMed]
63. Mortimer RK, Romano P, Suzzi G, Polsinelli M. Genome renewal: a new phenomenon revealed from a genetic study of 43 strains of Saccharomyces cerevisiae derived from natural fermentation of grape musts. Yeast. 1994;10:1543–1552. [PubMed]
64. Demogines A, Smith E, Kruglyak L, Alani E. Incompatibilities Involving Yeast Mismatch Repair Genes: A Role for Genetic Modifiers and Implications for Disease Penetrance and Variation in Genomic Mutation Rates. PLoS Genet. 2008;4:e1000103. doi:10.1371/journal.pgen.1000103. [PMC free article] [PubMed]
65. Heck JA, Argueso JL, Gemici Z, Reeves RG, Bernard A, et al. Negative epistasis between natural variants of the Saccharomyces cerevisiae MLH1 and PMS1 genes results in a defect in mismatch repair. Proc Natl Acad Sci USA. 2006;103:3256–3261. [PMC free article] [PubMed]
66. Carro D, Pina B. Genetic analysis of the karyotype instability in natural wine yeast strains. Yeast. 2001;18:1457–1470. [PubMed]
67. Carro D, Bartra E, Pina B. Karyotype rearrangements in a wine yeast strain by rad52-dependent and rad52-independent mechanisms. Appl Environ Microbiol. 2003;69:2161–2165. [PMC free article] [PubMed]
68. Fabre E, Muller H, Therizols P, Lafontaine I, Dujon B, et al. Comparative genomics in hemiascomycete yeasts: Evolution of sex, silencing, and subtelomeres. Mol Biol Evo. 2005;22:856–873. [PubMed]
69. Piskur J, Langkjaer RB. Yeast genome sequencing: the power of comparative genomics. Mol Microbiol. 2004;53:381–389. [PubMed]
70. Barkai N, Rose MD, Wingreen NS. Protease helps yeast find mating partners. Nature. 1998;396:422–423. [PubMed]
71. Wolfe KH, Shields DC. Molecular evidence for an ancient duplication of the entire yeast genome. Nature. 1997;387:708–713. [PubMed]
72. Mortimer RK. Evolution and variation of the yeast (Saccharomyces) genome. Genome Research. 2000;10:403–409. [PubMed]
73. Bell G. Kirkpatrick M, editor. The comparative biology of the alteration of generations. 1994. Lectures on mathematics in the life sciences: theories for the evolution of haploid-diploid life cycles: Am Math Soc, Providence, R. I. pp 1-26.
74. Mccullough J, Herskowitz I. Mating Pheromones of Saccharomyces kluyveri - Pheromone Interactions between Saccharomyces kluyveri and Saccharomyces cerevisiae. J Bacteriol. 1979;138:146–154. [PMC free article] [PubMed]
75. Winge LO. Saccharomycodes ludwigii Hansen, a balanced heterozygote. C R Trav Lab Carlsberg Ser Physiol. 1939;22:357–380.
76. McMurray MA, Gottschling DE. An age-induced switch to a hyper-recombinational state. Science. 2003;301:1908–1911. [PubMed]
77. Wilke CO, Wang JL, Ofria C, Lenski RE, Adami C. Evolution of digital organisms at high mutation rates leads to survival of the flattest. Nature. 2001;412:331–333. [PubMed]
78. Elena SF, Wilke CO, Ofria C, Lenski RE. Effects of population size and mutation rate on the evolution of mutational robustness. Evolution. 2007;61:666–674. [PubMed]
79. Wilke CO, Adami C. Evolution of mutational robustness. Mut Res. 2003;522:3–11. [PubMed]
80. Fraser HB, Hirsh AE, Giaever G, Kumm J, Eisen MB. Noise minimization in eukaryotic gene expression. PLoS Biol. 2004;2:e137. doi:10.1371/journal.pbio.0020137. [PMC free article] [PubMed]
81. Newman JR, Ghaemmaghami S, Ihmels J, Breslow DK, Noble M, et al. Single-cell proteomic analysis of S. cerevisiae reveals the architecture of biological noise. Nature. 2006;441:840–846. [PubMed]
82. Nishant KT, Rao MRS. Molecular features of meiotic recombination hot spots. BioEssays. 2006;28:45–56. [PubMed]
83. Raser JM, O'Shea EK. Noise in gene expression: origins, consequences, and control. Science. 2005;309:2010–2013. [PMC free article] [PubMed]
84. Deutschbauer AM, Jaramillo DF, Proctor M, Kumm J, Hillenmeyer ME, et al. Mechanisms of haploinsufficiency revealed by genome-wide profiling in yeast. Genetics. 2005;169:1915–1925. [PMC free article] [PubMed]
85. LIU B, Nicolaides NC, Markowitz S, Willson JKV, Parsons RE, et al. Mismatch Repair Gene Defects in Sporadic Colorectal Cancers with Microsatellite Instability. Nature Genet. 1995;9:48–55. [PubMed]
86. Fishel R, Lescoe MK, Rao MRS, Copeland NG, Jenkins Na, et al. The Human Mutator Gene Homolog Msh2 and Its Association with Hereditary Nonpolyposis Colon-Cancer. Cell. 1993;75:1027–1038. [PubMed]
87. Crespi B, Summers K. Evolutionary biology of cancer. Trends Ecol Evo. 2005;20:545–552. [PubMed]
88. Cahill DP, Kinzler KW, Vogelstein B, Lengauer C. Genetic instability and darwinian selection in tumours. Trends Biochem Sci. 1999;24:M57–M60. [PubMed]
89. Janke C, Magiera MM, Rathfelder N, Taxis C, Reber S, et al. A versatile toolbox for PCR-based tagging of yeast genes: new fluorescent proteins, more markers and promoter substitution cassettes. Yeast. 2004;21:947–962. [PubMed]
90. Kane SM, Roth R. Carbohydrate metabolism during ascospore development in yeast. J Bacteriol. 1974;118:8–14. [PMC free article] [PubMed]
91. Kurtzman CP, Fell JW. The yeasts: A taxonomic study; In: Kurtzman CP, Fell JW, editors. Elsevier; 1997.
92. Housworth EA, Stahl FW. Crossover interference in humans. Am J Hum Genet. 2003;73:188–197. [PMC free article] [PubMed]
93. Copenhaver GP, Housworth EA, Stahl FW. Crossover interference in Arabidopsis. Genetics. 2002;160:1631–1639. [PMC free article] [PubMed]

Articles from PLoS Genetics are provided here courtesy of Public Library of Science
PubReader format: click here to try

Formats:

Related citations in PubMed

See reviews...See all...

Cited by other articles in PMC

See all...

Links

Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...