Abstract:Yeasts are leading model organisms for mitochondrial genome studies. The explosion of complete sequence of yeast mitochondrial (mt) genomes revealed a wide diversity of organization and structure between species. Recently, genome-wide polymorphism survey on the mt genome of isolates of a single species, Lachancea kluyveri, was also performed. To compare the mitochondrial genome evolution at two hierarchical levels: within and among closely related species, we focused on five species of the Lachancea genus, whi… Show more
“…In L. kluyveri , a recent study found evidence for mobility of both cox1 and cob introns, noting presence/absence polymorphisms for three out of four cob and three out of five cox1 introns (Jung et al 2012). In line with widespread mobility in this species, all introns with the exception of the first cob intron encode endonucleases (Friedrich et al 2012). As predicted under a model where gene identity is secondary but mobility plays a pivotal role in nonrandom nucleotide diversity at intron–exon boundaries, we observe SNP density gradients across both cob (τ = −0.21, P = 0.03, Figure 2D) and cox1 exons (τ = −0.29, P = 0.002) in L. kluyveri , whereas in S. pombe a negative SNP gradient is evident for cob (τ = −0.31, P = 0.002) but not cox1 (τ = 0.16, P = 0.1).…”
“…In L. kluyveri , a recent study found evidence for mobility of both cox1 and cob introns, noting presence/absence polymorphisms for three out of four cob and three out of five cox1 introns (Jung et al 2012). In line with widespread mobility in this species, all introns with the exception of the first cob intron encode endonucleases (Friedrich et al 2012). As predicted under a model where gene identity is secondary but mobility plays a pivotal role in nonrandom nucleotide diversity at intron–exon boundaries, we observe SNP density gradients across both cob (τ = −0.21, P = 0.03, Figure 2D) and cox1 exons (τ = −0.29, P = 0.002) in L. kluyveri , whereas in S. pombe a negative SNP gradient is evident for cob (τ = −0.31, P = 0.002) but not cox1 (τ = 0.16, P = 0.1).…”
“…Few population genetic investigations on intraspecific mtDNAs in yeasts exist [45–47], and none for Saccharomyces species. To provide a window onto recent evolutionary changes in the mtDNA, we compared the intraspecific genetic variation in mitochondrial genomes from 100 strains of S. cerevisiae.…”
BackgroundRigorous study of mitochondrial functions and cell biology in the budding yeast, Saccharomyces cerevisiae has advanced our understanding of mitochondrial genetics. This yeast is now a powerful model for population genetics, owing to large genetic diversity and highly structured populations among wild isolates. Comparative mitochondrial genomic analyses between yeast species have revealed broad evolutionary changes in genome organization and architecture. A fine-scale view of recent evolutionary changes within S. cerevisiae has not been possible due to low numbers of complete mitochondrial sequences.ResultsTo address challenges of sequencing AT-rich and repetitive mitochondrial DNAs (mtDNAs), we sequenced two divergent S. cerevisiae mtDNAs using a single-molecule sequencing platform (PacBio RS). Using de novo assemblies, we generated highly accurate complete mtDNA sequences. These mtDNA sequences were compared with 98 additional mtDNA sequences gathered from various published collections. Phylogenies based on mitochondrial coding sequences and intron profiles revealed that intraspecific diversity in mitochondrial genomes generally recapitulated the population structure of nuclear genomes. Analysis of intergenic sequence indicated a recent expansion of mobile elements in certain populations. Additionally, our analyses revealed that certain populations lacked introns previously believed conserved throughout the species, as well as the presence of introns never before reported in S. cerevisiae.ConclusionsOur results revealed that the extensive variation in S. cerevisiae mtDNAs is often population specific, thus offering a window into the recent evolutionary processes shaping these genomes. In addition, we offer an effective strategy for sequencing these challenging AT-rich mitochondrial genomes for small scale projects.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-015-1664-4) contains supplementary material, which is available to authorized users.
“…Recent report suggested that the alteration of the gene order within yeast genera could be related to the mitochondrial genome size (Sulo et al 2017). While the Lachancea and Yarrowia clades, with mitochondrial genome less than 50 kb, show high synteny across species (Friedrich et al 2012;Gaillardin et al 2012), the Saccharomyces clade (mitochondrial genome size > 65 kb) is more prone to rearrangements (Sulo et al 2017). Indeed structural rearrangements were also detected in the mitochondrial genome of S. paradoxus (Yue et al 2017).…”
Section: Structural Rearrangements Are Rare In Mitochondrial Genomesmentioning
AbstractMitochondria are essential organelles partially regulated by their own genomes. The mitochondrial genome maintenance and inheritance differ from nuclear genome, potentially uncoupling their evolutionary trajectories. Here, we analysed mitochondrial sequences obtained from the 1,011 Saccharomyces cerevisiae strain collection and identified pronounced differences with their nuclear genome counterparts. In contrast with most fungal species, S. cerevisiae mitochondrial genomes show higher genetic diversity compared to the nuclear genomes. Strikingly, mitochondrial genomes appear to be highly admixed, resulting in a complex interconnected phylogeny with weak grouping of isolates, whereas interspecies introgressions are very rare. Complete genome assemblies revealed that structural rearrangements are nearly absent with rare inversions detected. We tracked introns variation in COX1 and COB to infer gain and loss events throughout the species evolutionary history. Mitochondrial genome copy number is connected with the nuclear genome and linearly scale up with ploidy. We observed rare cases of naturally occurring mitochondrial DNA loss, petite, with a subset of them that do not suffer fitness growth defects. Overall, our results illustrate how differences in the biology of two genomes coexisting in the same cells can lead to discordant evolutionary histories.
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