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Overdominant Mutations Restrict Adaptive Loss of Heterozygosity at Linked Loci

Loss of heterozygosity is a common mode of adaptation in asexual diploid populations. Because mitotic recombination frequently extends the full length of a chromosome arm, the selective benefit of loss of heterozygosity may be constrained by linked heterozygous mutations. In a previous laboratory ev...

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Autores principales: Fisher, Kaitlin J, Vignogna, Ryan C, Lang, Gregory I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8382679/
https://www.ncbi.nlm.nih.gov/pubmed/34363476
http://dx.doi.org/10.1093/gbe/evab181
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author Fisher, Kaitlin J
Vignogna, Ryan C
Lang, Gregory I
author_facet Fisher, Kaitlin J
Vignogna, Ryan C
Lang, Gregory I
author_sort Fisher, Kaitlin J
collection PubMed
description Loss of heterozygosity is a common mode of adaptation in asexual diploid populations. Because mitotic recombination frequently extends the full length of a chromosome arm, the selective benefit of loss of heterozygosity may be constrained by linked heterozygous mutations. In a previous laboratory evolution experiment with diploid yeast, we frequently observed homozygous mutations in the WHI2 gene on the right arm of Chromosome XV. However, when heterozygous mutations arose in the STE4 gene, another common target on Chromosome XV, loss of heterozygosity at WHI2 was not observed. Here, we show that mutations at WHI2 are partially dominant and that mutations at STE4 are overdominant. We test whether beneficial heterozygous mutations at these two loci interfere with one another by measuring loss of heterozygosity at WHI2 over 1,000 generations for ∼300 populations that differed initially only at STE4 and WHI2. We show that the presence of an overdominant mutation in STE4 reduces, but does not eliminate, loss of heterozygosity at WHI2. By sequencing 40 evolved clones, we show that populations with linked overdominant and partially dominant mutations show less parallelism at the gene level, more varied evolutionary outcomes, and increased rates of aneuploidy. Our results show that the degree of dominance and the phasing of heterozygous beneficial mutations can constrain loss of heterozygosity along a chromosome arm, and that conflicts between partially dominant and overdominant mutations can affect evolutionary outcomes.
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spelling pubmed-83826792021-08-24 Overdominant Mutations Restrict Adaptive Loss of Heterozygosity at Linked Loci Fisher, Kaitlin J Vignogna, Ryan C Lang, Gregory I Genome Biol Evol Research Article Loss of heterozygosity is a common mode of adaptation in asexual diploid populations. Because mitotic recombination frequently extends the full length of a chromosome arm, the selective benefit of loss of heterozygosity may be constrained by linked heterozygous mutations. In a previous laboratory evolution experiment with diploid yeast, we frequently observed homozygous mutations in the WHI2 gene on the right arm of Chromosome XV. However, when heterozygous mutations arose in the STE4 gene, another common target on Chromosome XV, loss of heterozygosity at WHI2 was not observed. Here, we show that mutations at WHI2 are partially dominant and that mutations at STE4 are overdominant. We test whether beneficial heterozygous mutations at these two loci interfere with one another by measuring loss of heterozygosity at WHI2 over 1,000 generations for ∼300 populations that differed initially only at STE4 and WHI2. We show that the presence of an overdominant mutation in STE4 reduces, but does not eliminate, loss of heterozygosity at WHI2. By sequencing 40 evolved clones, we show that populations with linked overdominant and partially dominant mutations show less parallelism at the gene level, more varied evolutionary outcomes, and increased rates of aneuploidy. Our results show that the degree of dominance and the phasing of heterozygous beneficial mutations can constrain loss of heterozygosity along a chromosome arm, and that conflicts between partially dominant and overdominant mutations can affect evolutionary outcomes. Oxford University Press 2021-08-07 /pmc/articles/PMC8382679/ /pubmed/34363476 http://dx.doi.org/10.1093/gbe/evab181 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Fisher, Kaitlin J
Vignogna, Ryan C
Lang, Gregory I
Overdominant Mutations Restrict Adaptive Loss of Heterozygosity at Linked Loci
title Overdominant Mutations Restrict Adaptive Loss of Heterozygosity at Linked Loci
title_full Overdominant Mutations Restrict Adaptive Loss of Heterozygosity at Linked Loci
title_fullStr Overdominant Mutations Restrict Adaptive Loss of Heterozygosity at Linked Loci
title_full_unstemmed Overdominant Mutations Restrict Adaptive Loss of Heterozygosity at Linked Loci
title_short Overdominant Mutations Restrict Adaptive Loss of Heterozygosity at Linked Loci
title_sort overdominant mutations restrict adaptive loss of heterozygosity at linked loci
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8382679/
https://www.ncbi.nlm.nih.gov/pubmed/34363476
http://dx.doi.org/10.1093/gbe/evab181
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