Abstract

Killer toxins are extracellular antifungal proteins that are produced by a wide variety of fungi, including Saccharomyces yeasts. Although many Saccharomyces killer toxins have been previously identified, their evolutionary origins remain uncertain given that many of these genes have been mobilized by double-stranded RNA (dsRNA) viruses. A survey of yeasts from the Saccharomyces genus has identified a novel killer toxin with a unique spectrum of activity produced by Saccharomyces paradoxus. The expression of this killer toxin is associated with the presence of a dsRNA totivirus and a satellite dsRNA. Genetic sequencing of the satellite dsRNA confirmed that it encodes a killer toxin with homology to the canonical ionophoric K1 toxin from Saccharomyces cerevisiae and has been named K1-like (K1L). Genomic homologs of K1L were identified in six non-Saccharomyces yeast species of the Saccharomycotina subphylum, predominantly in subtelomeric regions of the genome. When ectopically expressed in S. cerevisiae from cloned cDNAs, both K1L and its homologs can inhibit the growth of competing yeast species, confirming the discovery of a family of biologically active K1-like killer toxins. The sporadic distribution of these genes supports their acquisition by horizontal gene transfer followed by diversification. The phylogenetic relationship between K1L and its genomic homologs suggests a common ancestry and gene flow via dsRNAs and DNAs across taxonomic divisions. This appears to enable the acquisition of a diverse arsenal of killer toxins by different yeast species for potential use in niche competition.

Highlights

  • Many different species of fungi have been observed to produce proteinaceous killer toxins that inhibit the growth of competing fungal species [1,2,3,4,5,6,7,8,9,10]

  • Antifungal killer toxins produced by Saccharomyces yeasts can be found mostly encoded by cytoplasmic double-stranded RNAs rather than the DNA genome

  • The common ancestry of K1L and homologous killer toxins suggests the transfer of these genes via double-stranded RNA (dsRNA) and DNAs between different yeast species that inhabit similar natural and artificial environments

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Summary

Introduction

Many different species of fungi have been observed to produce proteinaceous killer toxins that inhibit the growth of competing fungal species [1,2,3,4,5,6,7,8,9,10]. There is evidence to support the sporadic genomic capture of killer toxins that are encoded by DNAs and RNAs that are derived from plasmids, viruses, and satellites [19,20]. These examples suggest that mobilization of killer toxins can occur by different mechanisms and that extrachromosomal elements play a role in gene flow between species

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