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Recombination, selection, and the evolution of tandem gene arrays
Multigene families—immunity genes or sensory receptors, for instance—are often subject to diversifying selection. Allelic diversity may be favored not only through balancing or frequency-dependent selection at individual loci but also by associating different alleles in multicopy gene families. Usin...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9252282/ https://www.ncbi.nlm.nih.gov/pubmed/35460227 http://dx.doi.org/10.1093/genetics/iyac052 |
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author | Otto, Moritz Zheng, Yichen Wiehe, Thomas |
author_facet | Otto, Moritz Zheng, Yichen Wiehe, Thomas |
author_sort | Otto, Moritz |
collection | PubMed |
description | Multigene families—immunity genes or sensory receptors, for instance—are often subject to diversifying selection. Allelic diversity may be favored not only through balancing or frequency-dependent selection at individual loci but also by associating different alleles in multicopy gene families. Using a combination of analytical calculations and simulations, we explored a population genetic model of epistatic selection and unequal recombination, where a trade-off exists between the benefit of allelic diversity and the cost of copy abundance. Starting from the neutral case, where we showed that gene copy number is Gamma distributed at equilibrium, we derived also the mean and shape of the limiting distribution under selection. Considering a more general model, which includes variable population size and population substructure, we explored by simulations mean fitness and some summary statistics of the copy number distribution. We determined the relative effects of selection, recombination, and demographic parameters in maintaining allelic diversity and shaping the mean fitness of a population. One way to control the variance of copy number is by lowering the rate of unequal recombination. Indeed, when encoding recombination by a rate modifier locus, we observe exactly this prediction. Finally, we analyzed the empirical copy number distribution of 3 genes in human and estimated recombination and selection parameters of our model. |
format | Online Article Text |
id | pubmed-9252282 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-92522822022-07-05 Recombination, selection, and the evolution of tandem gene arrays Otto, Moritz Zheng, Yichen Wiehe, Thomas Genetics Investigation Multigene families—immunity genes or sensory receptors, for instance—are often subject to diversifying selection. Allelic diversity may be favored not only through balancing or frequency-dependent selection at individual loci but also by associating different alleles in multicopy gene families. Using a combination of analytical calculations and simulations, we explored a population genetic model of epistatic selection and unequal recombination, where a trade-off exists between the benefit of allelic diversity and the cost of copy abundance. Starting from the neutral case, where we showed that gene copy number is Gamma distributed at equilibrium, we derived also the mean and shape of the limiting distribution under selection. Considering a more general model, which includes variable population size and population substructure, we explored by simulations mean fitness and some summary statistics of the copy number distribution. We determined the relative effects of selection, recombination, and demographic parameters in maintaining allelic diversity and shaping the mean fitness of a population. One way to control the variance of copy number is by lowering the rate of unequal recombination. Indeed, when encoding recombination by a rate modifier locus, we observe exactly this prediction. Finally, we analyzed the empirical copy number distribution of 3 genes in human and estimated recombination and selection parameters of our model. Oxford University Press 2022-04-23 /pmc/articles/PMC9252282/ /pubmed/35460227 http://dx.doi.org/10.1093/genetics/iyac052 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Genetics Society of America. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Investigation Otto, Moritz Zheng, Yichen Wiehe, Thomas Recombination, selection, and the evolution of tandem gene arrays |
title | Recombination, selection, and the evolution of tandem gene arrays |
title_full | Recombination, selection, and the evolution of tandem gene arrays |
title_fullStr | Recombination, selection, and the evolution of tandem gene arrays |
title_full_unstemmed | Recombination, selection, and the evolution of tandem gene arrays |
title_short | Recombination, selection, and the evolution of tandem gene arrays |
title_sort | recombination, selection, and the evolution of tandem gene arrays |
topic | Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9252282/ https://www.ncbi.nlm.nih.gov/pubmed/35460227 http://dx.doi.org/10.1093/genetics/iyac052 |
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