Conditional expression explains molecular evolution of social genes in a microbe

Autor: Christopher R. L. Thompson, Reinaldo Alves de Brito, Atahualpa Castillo Morales, Balint Stewart, Laurence D. Hurst, Nicole Gruenheit, Jennifer Engelmoer, Janaina Lima de Oliveira, Araxi O. Urrutia, Suzanne Battom Brown, Jason B. Wolf
Jazyk: angličtina
Rok vydání: 2019
Předmět:
Zdroj: Nature Communications
Nature Communications, Vol 10, Iss 1, Pp 1-12 (2019)
ISSN: 2041-1723
Popis: Conflict is thought to play a critical role in the evolution of social interactions by promoting diversity or driving accelerated evolution. However, despite our sophisticated understanding of how conflict shapes social traits, we have limited knowledge of how it impacts molecular evolution across the underlying social genes. Here we address this problem by analyzing the genome-wide impact of social interactions using genome sequences from 67 Dictyostelium discoideum strains. We find that social genes tend to exhibit enhanced polymorphism and accelerated evolution. However, these patterns are not consistent with conflict driven processes, but instead reflect relaxed purifying selection. This pattern is most likely explained by the conditional nature of social interactions, whereby selection on genes expressed only in social interactions is diluted by generations of inactivity. This dilution of selection by inactivity enhances the role of drift, leading to increased polymorphism and accelerated evolution, which we call the Red King process.
Genetic diversity in social genes is expected to be shaped by conflict. Here, the authors show that in Dictyostelium discoideum, social genes in fact exhibit diversification patterns consistent with relaxed purifying selection, likely due to their expression only in intermittent social generations.
Databáze: OpenAIRE