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Grieshop, K. H.

Publications and source records attributed to Grieshop, K. H..

2 recordsLinked to original sources

The capacity for adaptation to climate warming in an annual plant (Brassica rapa)

The persistence of a declining population in the face of environmental change may depend on how fast natural selection restores fitness, a process called "evolutionary rescue". In turn, evolutionary rescue depends on a populations adaptive potential. Fishers theorem states that a populations adaptive potential equals the additive genetic variance for fitness (VA(W)) divided by mean fitness [Formula]. Both the numerator and denominator of this rate can differ across environments even when holding allele frequencies constant. However, little is known about how these rates change in wild populations during adaptation, including changes in additive and dominance variance. We assessed the change in adaptive potential and dominance variance in fitness (VD(W)) for a Quebec population of wild mustard (Brassica rapa) under climate warming. We also assessed adaptive constraints that could arise from negative genetic correlations across environments. We grew a pedigreed population of 7000 plants under ambient and heated (+4{degrees}C) temperatures and estimated the change in [Formula], VA(W), VD(W), and the cross-environment genetic correlations (rA). As predicted, estimates of VA(W) and adaptive potentials were higher under heated conditions but non-significantly so. This is perhaps because, surprisingly, plants exposed to a warmer climate exhibited greater [Formula]. Nevertheless, increased fitness in the warmer environment suggests a plasticity-based short-term potential for adaptation, and that weak but non-significant genetic correlations across environments will enable slow on-going adaptation to warming. Overall, this population of B. rapa harbours existing genetic architecture to persist under warmer temperatures through pre-adaptation but not through evolutionary rescue.

evolutionary biology↗

Cis-regulatory variation in relation to sex and sexual dimorphism in Drosophila melanogaster

Much of sexual dimorphism is likely due to sex-biased gene expression, which results from differential regulation of a genome that is largely shared between males and females. Here we use allele-specific expression to explore cis-regulatory variation in Drosophila melanogaster in relation to sex. We develop a Bayesian framework to infer the transcriptome-wide joint distribution of cis-regulatory effects across the sexes. We use this approach to quantify transcriptome-wide sex differences in cis-regulatory effects as well as examine patterns of cis-regulatory variation with respect to two other levels of variation in sexual dimorphism: (i) across genes varying in their degree of sex-biased expression, and (ii) among tissues that vary in their degree of dimorphism (e.g., relatively low dimorphism in heads vs high dimorphism in gonads). We uncover evidence of widespread cis-regulatory variation in all tissues examined, with female-biased genes being especially enriched for this variation. A sizeable proportion of cis-regulatory variation is inferred to have sex-specific effects, with sex-dependent cis effects being much more frequent in gonads than in heads. Finally, we detect some genes with reversed allelic imbalance between the sexes. Such variants could provide a mechanism for sex-specific dominance reversals, a phenomenon important for sexually antagonistic balancing selection.

evolutionary biology↗