Functional and evolutionary constraints of wtf killer meiotic drivers

Abstract

Killer meiotic drivers are selfish DNA loci that sabotage the gametes that do not inherit them from a driver+/driver- heterozygote. These drivers often employ toxic proteins that target essential cellular functions to cause the destruction of driver- gametes. Identifying the mechanisms of drivers can expand our understanding of infertility and reveal novel insights about the cellular functions targeted by drivers. In this work, we explore the molecular mechanisms underlying the wtf family of killer meiotic drivers found in fission yeasts. Each wtf killer acts using a toxic Wtf^poison protein that can be neutralized by a corresponding Wtf^antidote protein. The wtf genes are rapidly evolving and extremely diverse. Here we found that self-assembly of Wtf^poison proteins is broadly conserved and associated with toxicity across the gene family, despite minimal amino acid conservation. In addition, we found the toxicity of Wtf^poison assemblies can be modulated by protein tags designed to increase or decrease the extent of the Wtf^poison assembly, implicating assembly size in toxicity. We also identified a conserved, critical role for the specific co-assembly of the Wtf^poison and Wtf^antidote proteins in promoting effective neutralization of Wtf^poison toxicity. Finally, we engineered wtf alleles that encode toxic Wtf^poison proteins that are not effectively neutralized by their corresponding Wtf^antidote proteins. The possibility of such self-destructive alleles reveals functional constraints on wtf evolution and suggests similar alleles could be cryptic contributors to infertility in fission yeast populations. As rapidly evolving killer meiotic drivers are widespread in eukaryotes, analogous self-killing drive alleles could contribute to sporadic infertility in many lineages.