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Bezmenova, A. V.

Publications and source records attributed to Bezmenova, A. V..

3 recordsLinked to original sources

Rapid divergence of male and female mitochondrial genomes in a basal protobranch bivalve Yoldia hyperborea

Doubly uniparental inheritance (DUI) of mitochondrial DNA (mtDNA) is a mode of mtDNA transmission whereby the male mitogenome is inherited predominately by males and the female mitogenome is inherited by females. DUI is unique to bivalve mollusks and has been identified in all major bivalve clades, including Protobranchia, the most basal bivalve subclade. Meanwhile, the mechanisms underlying the emergence and evolution of DUI remain poorly understood. Here, we focus on the early stages of divergence of male and female mitochondrial genomes by sequencing them in a basal Protobranchia species Yoldia hyperborea where they are characterized by low level of divergence, suggesting a recent origin of this system. Despite the relatively high relatedness of female and male genomes, we find that they have undergone rapid divergence both on the sequence and the structural level, including an origin of a novel gene, the ORFan, in the male genome. This novel gene is functional, as evidenced by the fact that it is transcribed and is subject to purifying selection. We show that this gene is a result of duplication and rapid evolution of another mitochondrial gene, NAD2. Additionally, the female mitogenome carries a duplicated cassette containing the cytochrome b gene, resulting in two different transcripts in female gonads both of which are subject to purifying selection, although their transcription levels differ by two orders of magnitude. These results showcase the rapid evolution of mitochondrial genes following their duplication, which occurred near the time of divergence of M- and F- mitochondrial genomes within a doubly uniparental inheritance system.

evolutionary biology↗

Rapid accumulation of mutations in growing mycelia of a hypervariable fungus Schizophyllum commune

The number of mutations that occur per nucleotide per generation varies between species by several orders of magnitude. In multicellular eukaryotes, the per generation mutation rate depends both on the per cell division mutation rate and on the number of germline cell divisions per generation. In a range of species, from fungi to humans, the number of germline cell divisions is lower than that of somatic cells, reducing the mutation burden on the offspring. The basidiomycete Schizophyllum commune has the highest level of genetic polymorphism known among eukaryotes. In a previous study, it was also found to have a high per generation mutation rate, probably contributing to its high polymorphism. However, this rate has been measured only in a breeding experiment on Petri dishes, and it is unclear how this result translates to natural populations. Here, we used an experimental design that measures the rate of accumulation of de novo mutations in a linearly growing mycelium. We show that S. commune accumulates mutations at a uniform rate of 1.4{middle dot}10-7 substitutions per nucleotide per meter of growth, which is 3 orders of magnitude higher than the corresponding rates in the oak Quercus robur and the fungus Armillaria gallica. This figure is consistent with the estimate obtained before, and suggests the lack of a dedicated germline in this system. If so, even a low per cell division mutation rate can translate into a very high per generation mutation rate when the number of cell divisions between consecutive meioses is large.

evolutionary biology↗

Prevalence of loss-of-function alleles does not correlate with lifetime fecundity and other life-history traits in metazoans

Natural selection is possible only because all species produce more offspring than what is needed to maintain the population. Still, the lifetime number of offspring varies widely across species. One can expect natural selection to be stronger in high-fecundity species. We analyzed the prevalence of loss-of-function alleles in 32 metazoan species and have found that, in contrast to this expectation, the strength of negative selection does not correlate with lifetime fecundity, as well as with other life-history traits. Perhaps, higher random mortality in high-fecundity species negates the effect of increased opportunity for selection.

evolutionary biology↗