Functional constraints of wtf killer meiotic drivers

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AI-generated summary by claude@2026-07, 2026-07-17

This study found that self-assembly of Wtf poison proteins is conserved and linked to toxicity, and that Wtf poison-antidote co-assembly is crucial for neutralization, revealing constraints on Wtf driver evolution.

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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. Author Summary Diploid organisms, such as humans, have two copies of most genes. Only one copy, however, is transmitted through gametes (e.g., sperm and egg) to any given offspring. Alternate copies of the same gene are expected to be equally represented in the gametes, resulting in random transmission to the next generation. However, some genes can "cheat" to be transmitted to more than half of the gametes, often at a cost to the host organism. Killer meiotic drivers are one such class of cheater genes that act by eliminating gametes lacking the driver. In this work, we studied the wtf family of killer meiotic drivers found in fission yeasts. Each wtf driver encodes a poison and an antidote protein to specifically kill gametes that do not inherit the driver. Through analyzing a large suite of diverse natural and engineered mutant wtf genes, we identified multiple properties—such as poison self-assembly and poison-antidote co-assembly—that can constrain poison toxicity and antidote rescue. These constraints could influence the evolution of wtf genes. Additionally, we discovered several incompatible wtf poison-antidote pairs, demonstrating expanded potential for self-killing wtf alleles. Such alleles could potentially arise spontaneously in populations cause infertility.

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europepmc
last seen: 2026-05-20T01:45:00.602351+00:00