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Experimental evolution of recombination and crossover interference in Drosophila caused by directional selection for stress-related traits

BACKGROUND: Population genetics predicts that tight linkage between new and/or pre-existing beneficial and deleterious alleles should decrease the efficiency of natural selection in finite populations. By decoupling beneficial and deleterious alleles and facilitating the combination of beneficial al...

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Autores principales: Aggarwal, Dau Dayal, Rashkovetsky, Eugenia, Michalak, Pawel, Cohen, Irit, Ronin, Yefim, Zhou, Dan, Haddad, Gabriel G., Korol, Abraham B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661966/
https://www.ncbi.nlm.nih.gov/pubmed/26614097
http://dx.doi.org/10.1186/s12915-015-0206-5
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author Aggarwal, Dau Dayal
Rashkovetsky, Eugenia
Michalak, Pawel
Cohen, Irit
Ronin, Yefim
Zhou, Dan
Haddad, Gabriel G.
Korol, Abraham B.
author_facet Aggarwal, Dau Dayal
Rashkovetsky, Eugenia
Michalak, Pawel
Cohen, Irit
Ronin, Yefim
Zhou, Dan
Haddad, Gabriel G.
Korol, Abraham B.
author_sort Aggarwal, Dau Dayal
collection PubMed
description BACKGROUND: Population genetics predicts that tight linkage between new and/or pre-existing beneficial and deleterious alleles should decrease the efficiency of natural selection in finite populations. By decoupling beneficial and deleterious alleles and facilitating the combination of beneficial alleles, recombination accelerates the formation of high-fitness genotypes. This may impose indirect selection for increased recombination. Despite the progress in theoretical understanding, interplay between recombination and selection remains a controversial issue in evolutionary biology. Even less satisfactory is the situation with crossover interference, which is a deviation of double-crossover frequency in a pair of adjacent intervals from the product of recombination rates in the two intervals expected on the assumption of crossover independence. Here, we report substantial changes in recombination and interference in three long-term directional selection experiments with Drosophila melanogaster: for desiccation (~50 generations), hypoxia, and hyperoxia tolerance (>200 generations each). RESULTS: For all three experiments, we found a high interval-specific increase of recombination frequencies in selection lines (up to 40–50 % per interval) compared to the control lines. We also discovered a profound effect of selection on interference as expressed by an increased frequency of double crossovers in selection lines. Our results show that changes in interference are not necessarily coupled with increased recombination. CONCLUSIONS: Our results support the theoretical predictions that adaptation to a new environment can promote evolution toward higher recombination. Moreover, this is the first evidence of selection for different recombination-unrelated traits potentially leading, not only to evolution toward increased crossover rates, but also to changes in crossover interference, one of the fundamental features of recombination. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-015-0206-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-46619662015-11-28 Experimental evolution of recombination and crossover interference in Drosophila caused by directional selection for stress-related traits Aggarwal, Dau Dayal Rashkovetsky, Eugenia Michalak, Pawel Cohen, Irit Ronin, Yefim Zhou, Dan Haddad, Gabriel G. Korol, Abraham B. BMC Biol Research Article BACKGROUND: Population genetics predicts that tight linkage between new and/or pre-existing beneficial and deleterious alleles should decrease the efficiency of natural selection in finite populations. By decoupling beneficial and deleterious alleles and facilitating the combination of beneficial alleles, recombination accelerates the formation of high-fitness genotypes. This may impose indirect selection for increased recombination. Despite the progress in theoretical understanding, interplay between recombination and selection remains a controversial issue in evolutionary biology. Even less satisfactory is the situation with crossover interference, which is a deviation of double-crossover frequency in a pair of adjacent intervals from the product of recombination rates in the two intervals expected on the assumption of crossover independence. Here, we report substantial changes in recombination and interference in three long-term directional selection experiments with Drosophila melanogaster: for desiccation (~50 generations), hypoxia, and hyperoxia tolerance (>200 generations each). RESULTS: For all three experiments, we found a high interval-specific increase of recombination frequencies in selection lines (up to 40–50 % per interval) compared to the control lines. We also discovered a profound effect of selection on interference as expressed by an increased frequency of double crossovers in selection lines. Our results show that changes in interference are not necessarily coupled with increased recombination. CONCLUSIONS: Our results support the theoretical predictions that adaptation to a new environment can promote evolution toward higher recombination. Moreover, this is the first evidence of selection for different recombination-unrelated traits potentially leading, not only to evolution toward increased crossover rates, but also to changes in crossover interference, one of the fundamental features of recombination. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-015-0206-5) contains supplementary material, which is available to authorized users. BioMed Central 2015-11-27 /pmc/articles/PMC4661966/ /pubmed/26614097 http://dx.doi.org/10.1186/s12915-015-0206-5 Text en © Aggarwal et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Aggarwal, Dau Dayal
Rashkovetsky, Eugenia
Michalak, Pawel
Cohen, Irit
Ronin, Yefim
Zhou, Dan
Haddad, Gabriel G.
Korol, Abraham B.
Experimental evolution of recombination and crossover interference in Drosophila caused by directional selection for stress-related traits
title Experimental evolution of recombination and crossover interference in Drosophila caused by directional selection for stress-related traits
title_full Experimental evolution of recombination and crossover interference in Drosophila caused by directional selection for stress-related traits
title_fullStr Experimental evolution of recombination and crossover interference in Drosophila caused by directional selection for stress-related traits
title_full_unstemmed Experimental evolution of recombination and crossover interference in Drosophila caused by directional selection for stress-related traits
title_short Experimental evolution of recombination and crossover interference in Drosophila caused by directional selection for stress-related traits
title_sort experimental evolution of recombination and crossover interference in drosophila caused by directional selection for stress-related traits
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4661966/
https://www.ncbi.nlm.nih.gov/pubmed/26614097
http://dx.doi.org/10.1186/s12915-015-0206-5
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