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The Linkage-Disequilibrium and Recombinational Landscape in Daphnia pulex
By revealing the influence of recombinational activity beyond what can be achieved with controlled crosses, measures of linkage disequilibrium (LD) in natural populations provide a powerful means of defining the recombinational landscape within which genes evolve. In one of the most comprehensive st...
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/PMC9642108/ https://www.ncbi.nlm.nih.gov/pubmed/36170345 http://dx.doi.org/10.1093/gbe/evac145 |
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author | Lynch, Michael Ye, Zhiqiang Urban, Lina Maruki, Takahiro Wei, Wen |
author_facet | Lynch, Michael Ye, Zhiqiang Urban, Lina Maruki, Takahiro Wei, Wen |
author_sort | Lynch, Michael |
collection | PubMed |
description | By revealing the influence of recombinational activity beyond what can be achieved with controlled crosses, measures of linkage disequilibrium (LD) in natural populations provide a powerful means of defining the recombinational landscape within which genes evolve. In one of the most comprehensive studies of this sort ever performed, involving whole-genome analyses on nearly 1,000 individuals of the cyclically parthenogenetic microcrustacean Daphnia pulex, the data suggest a relatively uniform pattern of recombination across the genome. Patterns of LD are quite consistent among populations; average rates of recombination are quite similar for all chromosomes; and although some chromosomal regions have elevated recombination rates, the degree of inflation is not large, and the overall spatial pattern of recombination is close to the random expectation. Contrary to expectations for models in which crossing-over is the primary mechanism of recombination, and consistent with data for other species, the distance-dependent pattern of LD indicates excessively high levels at both short and long distances and unexpectedly low levels of decay at long distances, suggesting significant roles for factors such as nonindependent mutation, population subdivision, and recombination mechanisms unassociated with crossing over. These observations raise issues regarding the classical LD equilibrium model widely applied in population genetics to infer recombination rates across various length scales on chromosomes. |
format | Online Article Text |
id | pubmed-9642108 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-96421082022-11-14 The Linkage-Disequilibrium and Recombinational Landscape in Daphnia pulex Lynch, Michael Ye, Zhiqiang Urban, Lina Maruki, Takahiro Wei, Wen Genome Biol Evol Research Article By revealing the influence of recombinational activity beyond what can be achieved with controlled crosses, measures of linkage disequilibrium (LD) in natural populations provide a powerful means of defining the recombinational landscape within which genes evolve. In one of the most comprehensive studies of this sort ever performed, involving whole-genome analyses on nearly 1,000 individuals of the cyclically parthenogenetic microcrustacean Daphnia pulex, the data suggest a relatively uniform pattern of recombination across the genome. Patterns of LD are quite consistent among populations; average rates of recombination are quite similar for all chromosomes; and although some chromosomal regions have elevated recombination rates, the degree of inflation is not large, and the overall spatial pattern of recombination is close to the random expectation. Contrary to expectations for models in which crossing-over is the primary mechanism of recombination, and consistent with data for other species, the distance-dependent pattern of LD indicates excessively high levels at both short and long distances and unexpectedly low levels of decay at long distances, suggesting significant roles for factors such as nonindependent mutation, population subdivision, and recombination mechanisms unassociated with crossing over. These observations raise issues regarding the classical LD equilibrium model widely applied in population genetics to infer recombination rates across various length scales on chromosomes. Oxford University Press 2022-09-28 /pmc/articles/PMC9642108/ /pubmed/36170345 http://dx.doi.org/10.1093/gbe/evac145 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of 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 (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 Lynch, Michael Ye, Zhiqiang Urban, Lina Maruki, Takahiro Wei, Wen The Linkage-Disequilibrium and Recombinational Landscape in Daphnia pulex |
title | The Linkage-Disequilibrium and Recombinational Landscape in Daphnia pulex |
title_full | The Linkage-Disequilibrium and Recombinational Landscape in Daphnia pulex |
title_fullStr | The Linkage-Disequilibrium and Recombinational Landscape in Daphnia pulex |
title_full_unstemmed | The Linkage-Disequilibrium and Recombinational Landscape in Daphnia pulex |
title_short | The Linkage-Disequilibrium and Recombinational Landscape in Daphnia pulex |
title_sort | linkage-disequilibrium and recombinational landscape in daphnia pulex |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9642108/ https://www.ncbi.nlm.nih.gov/pubmed/36170345 http://dx.doi.org/10.1093/gbe/evac145 |
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