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Conservation of the genome-wide recombination rate in white-footed mice
Despite being linked to the fundamental processes of chromosome segregation and offspring diversification, meiotic recombination rates vary within and between species. Recent years have seen progress in quantifying recombination rate evolution across multiple temporal and genomic scales. Nevertheles...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6781155/ https://www.ncbi.nlm.nih.gov/pubmed/31366913 http://dx.doi.org/10.1038/s41437-019-0252-9 |
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author | Peterson, April L. Miller, Nathan D. Payseur, Bret A. |
author_facet | Peterson, April L. Miller, Nathan D. Payseur, Bret A. |
author_sort | Peterson, April L. |
collection | PubMed |
description | Despite being linked to the fundamental processes of chromosome segregation and offspring diversification, meiotic recombination rates vary within and between species. Recent years have seen progress in quantifying recombination rate evolution across multiple temporal and genomic scales. Nevertheless, the level of variation in recombination rate within wild populations—a key determinant of evolution in this trait—remains poorly documented on the genomic scale. To address this notable gap, we used immunofluorescent cytology to quantify genome-wide recombination rates in males from a wild population of the white-footed mouse, Peromyscus leucopus. For comparison, we measured recombination rates in a second population of male P. leucopus raised in the laboratory and in male deer mice from the subspecies Peromyscus maniculatus bairdii. Although we found differences between individuals in the genome-wide recombination rate, levels of variation were low—within populations, between populations, and between species. Quantification of synaptonemal complex length and crossover positions along chromosome 1 using a novel automated approach also revealed conservation in broad-scale crossover patterning, including strong crossover interference. We propose stabilizing selection targeting recombination or correlated processes as the explanation for these patterns. |
format | Online Article Text |
id | pubmed-6781155 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-67811552019-10-09 Conservation of the genome-wide recombination rate in white-footed mice Peterson, April L. Miller, Nathan D. Payseur, Bret A. Heredity (Edinb) Article Despite being linked to the fundamental processes of chromosome segregation and offspring diversification, meiotic recombination rates vary within and between species. Recent years have seen progress in quantifying recombination rate evolution across multiple temporal and genomic scales. Nevertheless, the level of variation in recombination rate within wild populations—a key determinant of evolution in this trait—remains poorly documented on the genomic scale. To address this notable gap, we used immunofluorescent cytology to quantify genome-wide recombination rates in males from a wild population of the white-footed mouse, Peromyscus leucopus. For comparison, we measured recombination rates in a second population of male P. leucopus raised in the laboratory and in male deer mice from the subspecies Peromyscus maniculatus bairdii. Although we found differences between individuals in the genome-wide recombination rate, levels of variation were low—within populations, between populations, and between species. Quantification of synaptonemal complex length and crossover positions along chromosome 1 using a novel automated approach also revealed conservation in broad-scale crossover patterning, including strong crossover interference. We propose stabilizing selection targeting recombination or correlated processes as the explanation for these patterns. Springer International Publishing 2019-07-31 2019-10 /pmc/articles/PMC6781155/ /pubmed/31366913 http://dx.doi.org/10.1038/s41437-019-0252-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Peterson, April L. Miller, Nathan D. Payseur, Bret A. Conservation of the genome-wide recombination rate in white-footed mice |
title | Conservation of the genome-wide recombination rate in white-footed mice |
title_full | Conservation of the genome-wide recombination rate in white-footed mice |
title_fullStr | Conservation of the genome-wide recombination rate in white-footed mice |
title_full_unstemmed | Conservation of the genome-wide recombination rate in white-footed mice |
title_short | Conservation of the genome-wide recombination rate in white-footed mice |
title_sort | conservation of the genome-wide recombination rate in white-footed mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6781155/ https://www.ncbi.nlm.nih.gov/pubmed/31366913 http://dx.doi.org/10.1038/s41437-019-0252-9 |
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