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Kyriazis, C.

Publications and source records attributed to Kyriazis, C..

4 recordsLinked to original sources

The impact of non-neutral synonymous mutations when inferring selection on non-synonymous mutations

The distribution of fitness effects (DFE) describes the proportions of new mutations that have different effects on reproductive fitness. Accurate measurements of the DFE are important because the DFE is a fundamental parameter in evolutionary genetics and has implications for our understanding of other phenomena like complex disease or inbreeding depression. Current computational methods to infer the DFE for nonsynonymous mutations from natural variation first estimate demographic parameters from synonymous variants to control for the effects of demography and background selection. Then, conditional on these parameters, the DFE is then inferred for nonsynonymous mutations. This approach relies on the assumption that synonymous variants are neutrally evolving. However, some evidence points toward synonymous mutations having measurable effects on fitness. To test whether selection on synonymous mutations affects inference of the DFE of nonsynonymous mutations, we simulated several possible models of selection on synonymous mutations using SLiM and attempted to recover the DFE of nonsynonymous mutations using Fit{partial}a{partial}i, a common method for DFE inference. Our results show that the presence of selection on synonymous variants leads to incorrect inferences of recent population growth. Furthermore, under certain parameter combinations, inferences of the DFE can have an inflated proportion of highly deleterious nonsynonymous mutations. However, this bias can be eliminated if the correct demographic parameters are used for DFE inference instead of the biased ones inferred from synonymous variants. Our work demonstrates how unmodeled selection on synonymous mutations may affect downstream inferences of the DFE.

evolutionary biology↗

Quantifying the fraction of new mutations that are recessive lethal

The presence and impact of recessive lethal mutations has been widely documented in diploid outcrossing species. However, precise estimates in different species of the proportion of mutations that are recessive lethal remain limited. Here, we attempt to quantify the fraction of new mutations that are recessive lethal using Fit{partial}a{partial}i, a commonly-used method for inferring the distribution of fitness effects (DFE) using the site frequency spectrum. Using simulations, we demonstrate that Fit{partial}a{partial}i cannot accurately estimate the fraction of recessive lethal mutations, as expected given that Fit{partial}a{partial}i assumes that all mutations are additive by default. Consistent with the idea that mis-specification of the dominance model can explain this performance, we find that Fit{partial}a{partial}i can accurately infer the fraction of additive lethal mutations. Moreover, we demonstrate that in both additive and recessive cases, inference of the deleterious non-lethal portion of the DFE is minimally impacted by a small proportion (<10%) of lethal mutations. Finally, as an alternative approach to estimate the proportion of mutations that are recessive lethal, we employ models of mutation-selection-drift balance using existing genomic parameters and segregating recessive lethals estimates for humans and Drosophila melanogaster. In both species, we find that the segregating recessive lethal load can be explained by a very small fraction (<1%) of new nonsynonymous mutations being recessive lethal. Our results refute recent assertions of a much higher recessive lethal mutation fraction (4-5%), while highlighting the need for additional information on the joint distribution of selection and dominance coefficients.

evolutionary biology↗

Genomic underpinnings of population persistence in Isle Royale moose

Island ecosystems provide models to assess the impacts of isolation on population persistence. However, most studies of persistence have focused on a single species, without comparisons to other organisms they interact with in the ecosystem. The simple predator-prey system of moose and gray wolves on Isle Royale provides allows a direct contrast of genetic variation in a prey species with their natural predator. Wolves on Isle Royale exhibited signs of severe inbreeding depression, which nearly drove the population to extinction in 2019. In the relative absence of wolves, the moose population has thrived and exhibits no obvious signs of inbreeding depression despite being isolated for [~]120 years and having low genetic diversity. Here, we examine the genomic underpinnings of population persistence in the Isle Royale moose population. We document high levels of inbreeding in the population, roughly as high as the wolf population at the time of its decline. However, inbreeding in the moose population manifests in the form of intermediate-length runs of homozygosity indicative of gradual inbreeding, contrasting with the severe recent inbreeding observed in the wolf population. Using simulations, we demonstrate that this more gradual inbreeding in the moose population has resulted in an estimated 50% purging of the inbreeding load, helping to explain the continued persistence of the population. However, we also document notable increases in genetic load, which could eventually threaten population viability over the long term. Finally, we document low diversity in mainland North American moose populations due to a severe founder event occurring near the end of the Holocene. Overall, our results demonstrate a complex relationship between inbreeding, genetic diversity, and population viability that highlights the importance of maintaining isolated populations at moderate size to avert extinction from genetic factors. Significance statementIsolated wildlife populations face a high risk of extinction due in part to the deleterious consequences of inbreeding. Whether purifying natural selection can overcome these negative impacts by "purging" harmful recessive mutations is a topic of active debate. We characterized the extent of purging in an isolated moose population. Our results demonstrate signatures of gradual inbreeding in the population, ideal circumstances to facilitate purging. Using simulations, we demonstrate substantial potential for purging in the population, though we also show that fitness is reduced by small population size and inbreeding. Our findings provide insight into the mechanisms enabling persistence in isolated populations, with implications for conserving the growing number of isolated populations worldwide.

evolutionary biology↗

Diversification of a cryptic radiation, a closer look at Madagascar’s recently recognized bird family

Despite its status as a global biodiversity hotspot there is still much to be discovered about the birds of Madagascar, including a full accounting of species-level diversity and the avifaunas origins. The Bernieridae is a Malagasy endemic family that went unrecognized by science for decades and unnamed until 2010. This cryptic family has long represented a missing piece of the puzzle of the avian tree of life. We present the first comprehensive phylogeny of Bernieridae in order to examine its diversification history on Madagascar and its place within Passeriformes. In light of recent discoveries of cryptic species-level diversity in Madagascars vertebrate fauna, we used broad geographic sampling and integrative taxonomic methods to investigate the potential for cryptic lineages within every known species of the Bernieridae. Our approach combines phylogenomics using [~]4500 loci of ultraconserved elements (UCEs), genetic clustering of thousands of single nucleotide polymorphisms (SNPs), and statistical analysis of morphological variation. These methods yielded the discovery of two unrecognized species in the previously monotypic genus Bernieria, along with new insights into patterns of fine-scale endemism in Madagascars humid forests. Our phylogenomic analyses provide conclusive support for Donacobiidae and Bernieridae as sister families, a biogeographically intriguing result given that the former is restricted to the Neotropics. We found a significant decline in the rate of speciation over time on Madagascar, consistent with a model of adaptive radiation. Bernieridae therefore joins the Vangidae as a second avian adaptive radiation on the island of Madagascar. These insights into the evolution of Bernieridae represent a step forward in understanding the origins and diversity of Madagascars endemic avifauna.

evolutionary biology↗