A natural variant of the essential host gene MMS21 restricts the parasitic 2-micron plasmid in Saccharomyces cerevisiae

Author:

Hays Michelle12ORCID,Young Janet M2ORCID,Levan Paula F2,Malik Harmit S23ORCID

Affiliation:

1. Molecular and Cellular Biology program, University of Washington, Seattle, United States

2. Division of Basic Sciences & Fred Hutchinson Cancer Research Center, Seattle, United States

3. Howard Hughes Medical Institute, Fred Hutchinson Cancer Research Center, Seattle, United States

Abstract

Antagonistic coevolution with selfish genetic elements (SGEs) can drive evolution of host resistance. Here, we investigated host suppression of 2-micron (2μ) plasmids, multicopy nuclear parasites that have co-evolved with budding yeasts. We developed SCAMPR (Single-Cell Assay for Measuring Plasmid Retention) to measure copy number heterogeneity and 2μ plasmid loss in live cells. We identified threeS. cerevisiaestrains that lack endogenous 2μ plasmids and reproducibly inhibit mitotic plasmid stability. Focusing on the Y9 ragi strain, we determined that plasmid restriction is heritable and dominant. Using bulk segregant analysis, we identified a high-confidence Quantitative Trait Locus (QTL) with a single variant ofMMS21associated with increased 2μ instability.MMS21encodes a SUMO E3 ligase and an essential component of the Smc5/6 complex, involved in sister chromatid cohesion, chromosome segregation, and DNA repair. Our analyses leverage natural variation to uncover a novel means by which budding yeasts can overcome highly successful genetic parasites.

Funder

National Institute of General Medical Sciences

National Science Foundation

National Human Genome Research Institute

Howard Hughes Medical Institute

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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