by professor Leif Andersson Uppsala University, Texas A&M University, Swedish University of Agricultural Sciences
Professor Leif Andersson has devoted his research to investigate the connection and interplay between the genome, its regulation, and the occurring phenotype. In the current lecture he will give examples from natural populations of ruff (Philomachus pugnax) and Atlantic herring (Clupea harengus) where whole genome sequencing has given novel insight into the relationship between genetic and phenotypic variation.
Abstract: The possibility to assemble any genome and resequence multiple individuals from the same species has radically changed the field of evolutionary biology. In this presentation I will present how we have used whole genome sequencing to resolve two enigmas that have been under debate for decades. One concerns how it is possible that the three male morphs in the ruff with strikingly different mating strategies, plumage and body size can be inherited as a simple monogenic trait. The other concerns the Atlantic herring (Clupea harengus), which is one of the most abundant vertebrates on earth and constitutes a huge biomass in the North Atlantic. Earlier studies based on a limited number of genetic markers (isozymes and microsatellites) had hardly revealed any genetic differentiation at all between populations living in strikingly different environments, such as the Atlantic Ocean and the brackish Baltic Sea, or spawning on different times of the year (early spring to late fall). How is this possible? Whole genome sequencing of multiple populations has now revealed that the FST distribution in this species deviates significantly from the one expected under selective neutrality with the great majority of loci showing no genetic differentiation while a small percentage show highly significant differentiation. This makes this species an ideal model organism for detecting signatures of natural selection. These studies revealed a new enigma namely that the Atlantic herring has only a moderate nucleotide diversity (π=0.3%), “only” three-fold higher than humans, despite a huge census population size. The possible explanation for this enigma will be discussed.
The Volterra Lectures, named in honor of Vito Volterra, one of the first mathematical biologists, is a high-profile lecture series supported by Centre for Digital Life Norway (DLN). The current lecture is hosted by the Faculty of Mathematics and Natural Sciences, UiO. Everyone is welcome!