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Kozak, G. M.

Publications and source records attributed to Kozak, G. M..

4 recordsLinked to original sources

Leveraging the joint site frequency spectrum to detect genomic regions of early divergence

Detecting genomic loci underlying local adaptation and population divergence is a central goal in population genetics. Such loci have been detected in genomic data using a variety of approaches, but the statistical performance of these approaches can depend substantially on the frequencies of the alleles underlying phenotypic adaptation. In particular, multiple evolutionary modeling studies have shown that rare alleles of large effect can make substantial contributions to phenotypic differentiation in the early stages of adaptation, but most selection inference methods are not sensitive to rare alleles. We used simulations of evolutionary divergence to compare commonly-used FST scans to a likelihood-based approach that interrogates the whole frequency spectrum. We found that the likelihood-based approach outperforms FST when low frequency alleles play a substantial role in driving trait divergence. We applied both approaches to genomic data from Ostrinia nubilalis (the European Corn Borer), a species in which population-specific variation in circannual rhythms and mate preference phenotypes have driven recent reproductive isolation. The likelihood-based approach recovers previously discovered genomic loci and finds several new candidate regions that may be relevant for reproductive isolation between populations. Our findings demonstrate how the two-dimensional frequency spectrum may help to identify loci contributing to reproductive isolation in contexts when commonly used methods are less powerful.

evolutionary biology↗

Consequences of coupled barriers to gene flow for the build-up of genomic differentiation

Theory predicts that when different barriers to gene flow become coincident, their joint effects enhance reproductive isolation and genomic divergence beyond their individual effects, but empirical tests of this coupling hypothesis are rare. Here, we analyze patterns of gene exchange among populations of European corn borer moths that vary in the number of acting barriers, allowing for comparisons of genomic variation when barrier traits or loci are in coincident or independent states. We find that divergence is mainly restricted to barrier loci when populations differ by a single barrier, whereas the coincidence of temporal and behavioral barriers is associated with divergence of two chromosomes harboring barrier loci. Furthermore, differentiation at temporal barrier loci increases in the presence of behavioral divergence and differentiation at behavioral barrier loci increases in the presence of temporal divergence. Our results demonstrate how the joint action of coincident barrier effects leads to levels of genomic differentiation that far exceed those of single barriers acting alone, consistent with theory arguing that coupling allows indirect selection to combine with direct selection and thereby lead to a stronger overall barrier to gene flow. Thus, the state of barriers - independent or coupled - strongly influences the accumulation of genomic differentiation.

evolutionary biology↗

Genomic landscape of reproductive isolation in Lucania killifish: The role of sex chromosomes and salinity

Understanding how speciation occurs and how reproductive barriers contribute to population structure at a genomic scale requires elucidating the genetic architecture of reproductive isolating barriers. In particular, it is crucial to determine if loci underlying reproductive isolation are genetically linked or if they are located on sex chromosomes, which have unique inheritance and population genetic properties. Bluefin killifish (Lucania goodei) and rainwater killifish (L. parva) are closely related species that have diverged across a salinity gradient and are reproductively isolated by assortative mating, hybrid male infertility, viability of hybrid offspring at high salinities, as well as reduced overall fitness of F2 offspring and backcrosses to L. goodei. We conducted QTL mapping in backcrosses between L. parva and L. goodei to determine the genetic architecture of sex determination, mate attractiveness, fertility, and salinity tolerance. We find that the sex locus appears to be male determining and located on a chromosome that has undergone a Robertsonian fusion in L. parva relative to L. goodei. We find that the sex locus on the fused chromosome is involved in several genomic incompatibilities, which affect the survival of backcrossed offspring. Among the backcrossed offspring that survived to adulthood, we find that one QTL for male attractiveness to L. goodei females is closely linked to this sex locus on chromosome 1. Males homozygous for L. goodei alleles at the sex locus laid more eggs with L. goodei females. QTL associated with salinity tolerance were spread across the genome but did not tend to co-localize with reproductive isolation. Thus, speciation in this system appears to be driven by reinforcement and indirect selection against hybrids rather than direct natural selection for salinity tolerance. Our work adds to growing evidence that sex chromosome evolution may contribute to speciation.

evolutionary biology↗

Genomic basis of circannual rhythm in the European corn borer moth

Genetic variation in life-history timing allows populations to synchronize with seasonal cycles but little is known about the molecular mechanisms that produce differences in circannual rhythm in nature. Changes in diapause timing in the European corn borer moth (Ostrinia nubilalis) have facilitated rapid response to shifts in winter length encountered during range expansion and from climate change, with some populations emerging from diapause earlier to produce an additional generation per year. We identify genomic variation associated with changes in the time spent in winter diapause and show evidence that the circadian clock genes period (per) and pigment dispersing factor receptor (Pdfr) interact to underlie this adaptive polymorphism in circannual rhythm. Per and Pdfr are located within two epistatic QTL, strongly differ in allele frequency among individuals that pupate earlier or later, have the highest linkage disequilibrium among gene pairs in the QTL regions despite separation by > 4 megabases, and possess amino-acid changes likely to affect function. One per mutation in linkage disequilibrium with Pdfr creates a novel putative clock-cycle binding site found exclusively in populations that pupate later. We find associated changes in free-running daily circadian rhythm, with longer daily rhythms in individuals that end diapause early. These results support a modular connection between circadian and circannual timers and provide testable hypotheses about the physiological role of the circadian clock in seasonal synchrony. Winter length is expected to continually shorten from climate warming and we predict these gene candidates will be targets of selection for future adaptation and population persistence.

evolutionary biology↗