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| Funder | Biotechnology and Biological Sciences Research Council |
|---|---|
| Recipient Organization | University of Cambridge |
| Country | United Kingdom |
| Start Date | Mar 01, 2022 |
| End Date | Jan 31, 2026 |
| Duration | 1,432 days |
| Number of Grantees | 1 |
| Roles | Principal Investigator |
| Data Source | UKRI Gateway to Research |
| Grant ID | BB/V01451X/1 |
Animals are hugely varied in their colouration, which can be adapted for a multiplicity of functions including camouflage, warning, sexual signals and thermoregulation. Stable polymorphisms in colouration offer an opportunity to study evolutionary processes including natural selection, gene flow and genetic drift acting in the wild. In some cases, variation in colour is an external indicator of differences between individuals in their physiology, behaviour and other complex traits.
Such genetic correlations among colouration and other traits can be important for the maintenance of variation within populations. In some cases, such correlations are due to multiple genes in tight linkage, so-called supergenes, but in other cases complex polymorphisms seem to have a very simple genetic basis. Here we will study genetic correlations in the wood tiger moth, Arctia plantaginis.
Males have either yellow or white hindwings, but these morphs also differ in behaviour, pheromones, immune responses and defensive chemistry. In contrast, females show continuous variation in hindwing colour, which is negatively correlated with larval warning colour. The system has many advantages for genetic analysis, being tractable to rear in large numbers and well-studied in the wild.
Preliminary work on the male polymorphism has identified a narrow genomic region that controls morph differences, containing just six genes. Here we will identify the gene responsible for the yellow/white polymorphism using gene expression and gene knockdown experiments. Next, we will test whether the complex traits that differ between morphs vary as pleiotropic effects of the major yellow/white locus, or whether they represent variation at other loci perhaps maintained in linkage disequilibrium.
We will also explore the genetic architecture of trade-offs in adult and larval colour traits that show more continuous variation. Here, we will take advantage of large pedigrees that are already available for genetic analysis. Additional breeding and phenotyping of families will be carried out with our Co-I Johanna Mappes in Finland.
Finally, we will take advantage of large numbers of wild caught individuals already available to study patterns of genetic variation in the wild. In particular, we will test for signatures of balancing selection at loci controlling polymorphic and variable colour phenotypes. We will also test for patterns of association (linkage disequilibrium) between loci controlling multiple traits.
In summary, this project offers an exciting opportunity to develop a new evolutionary genetic system. The wood tiger moth is already well studied in the field and laboratory. We know a great deal about its interaction with predators and with the biotic environment, as well as its behaviour and eco-physiology.
However, despite many advantages for genetic analysis including ease of rearing in large numbers and relatively small genome, little genetic analysis has been carried out to date. Here we will explore the genetic basis for key traits in this system and explore the action of natural selection in wild populations at a genetic level. This project has the potential for developing an exciting new text-book example, in which evolutionary forces can be studied through from genotype to phenotype to fitness in the wild.
University of Cambridge
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