The evolution of self‐fertilisation from outcrossing is one of the most frequent evolutionary transitions in hermaphrodite species of plants, animals and fungi. Accordingly, a large body of theoretical and empirical studies has been dedicated to understand the impact of selfing on population genetics and genome evolution. Compared to outcrossing, selfing reduces heterozygosity, effective recombination and migration rate and increases genetic drift. As a consequence, selfing species are expected to show reduced and more structured genetic diversity, genomic degradation and low adaptive potential because they should respond less efficiently to natural selection. Although selfing can have immediate advantages and be selected for, all detrimental genetic effects are thought to drive selfing lineages to extinction on the long run. Human activities (e.g. domestication and breeding, ecosystem alterations) can also induce mating system shifts that could potentially threaten long‐term population viability.
Key Concepts
The transition from outcrossing to selfing affects fundamental population genetics parameters that influence the evolutionary trajectory of populations and species.
Selfing increases homozygosity, which reveals recessive deleterious alleles causing inbreeding depression.
Selfing reduces the effective recombination, which increases genome‐wide linkage disequilibrium.
Selfing increases genetic structure by reducing gene flow.
Selfing reduces the effective population size, making selfing species less diverse and less efficient in responding to selection than outcrossing ones.
The outcome of selection in selfing species depends on the interplay among dominance level and selection strength of mutations and the initial conditions (new mutations or preexisting variation).
In selfing organisms, sexual conflicts and the spread of selfish genetic elements are attenuated.
Overall, the genome of selfing species is prone to the accumulation of deleterious mutations and to low rates of fixation of beneficial mutations, which should make selfing an evolutionary ‘dead‐end’ strategy.
The genetic consequences induced by self‐fertilisation have practical implications for human activities linked to the conservation and management of natural and cultivated resources.