Cargando…

Recombination rate plasticity: revealing mechanisms by design

For over a century, scientists have known that meiotic recombination rates can vary considerably among individuals, and that environmental conditions can modify recombination rates relative to the background. A variety of external and intrinsic factors such as temperature, age, sex and starvation ca...

Descripción completa

Detalles Bibliográficos
Autores principales: Stevison, Laurie S., Sefick, Stephen, Rushton, Chase, Graze, Rita M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698621/
https://www.ncbi.nlm.nih.gov/pubmed/29109222
http://dx.doi.org/10.1098/rstb.2016.0459
_version_ 1783280796396683264
author Stevison, Laurie S.
Sefick, Stephen
Rushton, Chase
Graze, Rita M.
author_facet Stevison, Laurie S.
Sefick, Stephen
Rushton, Chase
Graze, Rita M.
author_sort Stevison, Laurie S.
collection PubMed
description For over a century, scientists have known that meiotic recombination rates can vary considerably among individuals, and that environmental conditions can modify recombination rates relative to the background. A variety of external and intrinsic factors such as temperature, age, sex and starvation can elicit ‘plastic’ responses in recombination rate. The influence of recombination rate plasticity on genetic diversity of the next generation has interesting and important implications for how populations evolve. Further, many questions remain regarding the mechanisms and molecular processes that contribute to recombination rate plasticity. Here, we review 100 years of experimental work on recombination rate plasticity conducted in Drosophila melanogaster. We categorize this work into four major classes of experimental designs, which we describe via classic studies in D. melanogaster. Based on these studies, we highlight molecular mechanisms that are supported by experimental results and relate these findings to studies in other systems. We synthesize lessons learned from this model system into experimental guidelines for using recent advances in genotyping technologies, to study recombination rate plasticity in non-model organisms. Specifically, we recommend (1) using fine-scale genome-wide markers, (2) collecting time-course data, (3) including crossover distribution measurements, and (4) using mixed effects models to analyse results. To illustrate this approach, we present an application adhering to these guidelines from empirical work we conducted in Drosophila pseudoobscura. This article is part of the themed issue ‘Evolutionary causes and consequences of recombination rate variation in sexual organisms’.
format Online
Article
Text
id pubmed-5698621
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher The Royal Society
record_format MEDLINE/PubMed
spelling pubmed-56986212017-11-29 Recombination rate plasticity: revealing mechanisms by design Stevison, Laurie S. Sefick, Stephen Rushton, Chase Graze, Rita M. Philos Trans R Soc Lond B Biol Sci Articles For over a century, scientists have known that meiotic recombination rates can vary considerably among individuals, and that environmental conditions can modify recombination rates relative to the background. A variety of external and intrinsic factors such as temperature, age, sex and starvation can elicit ‘plastic’ responses in recombination rate. The influence of recombination rate plasticity on genetic diversity of the next generation has interesting and important implications for how populations evolve. Further, many questions remain regarding the mechanisms and molecular processes that contribute to recombination rate plasticity. Here, we review 100 years of experimental work on recombination rate plasticity conducted in Drosophila melanogaster. We categorize this work into four major classes of experimental designs, which we describe via classic studies in D. melanogaster. Based on these studies, we highlight molecular mechanisms that are supported by experimental results and relate these findings to studies in other systems. We synthesize lessons learned from this model system into experimental guidelines for using recent advances in genotyping technologies, to study recombination rate plasticity in non-model organisms. Specifically, we recommend (1) using fine-scale genome-wide markers, (2) collecting time-course data, (3) including crossover distribution measurements, and (4) using mixed effects models to analyse results. To illustrate this approach, we present an application adhering to these guidelines from empirical work we conducted in Drosophila pseudoobscura. This article is part of the themed issue ‘Evolutionary causes and consequences of recombination rate variation in sexual organisms’. The Royal Society 2017-12-19 2017-11-06 /pmc/articles/PMC5698621/ /pubmed/29109222 http://dx.doi.org/10.1098/rstb.2016.0459 Text en © 2017 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Articles
Stevison, Laurie S.
Sefick, Stephen
Rushton, Chase
Graze, Rita M.
Recombination rate plasticity: revealing mechanisms by design
title Recombination rate plasticity: revealing mechanisms by design
title_full Recombination rate plasticity: revealing mechanisms by design
title_fullStr Recombination rate plasticity: revealing mechanisms by design
title_full_unstemmed Recombination rate plasticity: revealing mechanisms by design
title_short Recombination rate plasticity: revealing mechanisms by design
title_sort recombination rate plasticity: revealing mechanisms by design
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698621/
https://www.ncbi.nlm.nih.gov/pubmed/29109222
http://dx.doi.org/10.1098/rstb.2016.0459
work_keys_str_mv AT stevisonlauries recombinationrateplasticityrevealingmechanismsbydesign
AT sefickstephen recombinationrateplasticityrevealingmechanismsbydesign
AT rushtonchase recombinationrateplasticityrevealingmechanismsbydesign
AT grazeritam recombinationrateplasticityrevealingmechanismsbydesign