Adaptive Control of the Meiotic Recombination Landscape by DNA Site-dependent Hotspots With Implications for Evolution

Meiosis is an essential component of the sexual life cycle in eukaryotes. The independent assortment of chromosomes in meiosis increases genetic diversity at the level of whole chromosomes and meiotic recombination increases genetic diversity within chromosomes. The resulting variability fuels evolu...

Full description

Bibliographic Details
Main Authors: Reine U. Protacio, Mari K. Davidson, Wayne P. Wahls
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-06-01
Series:Frontiers in Genetics
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fgene.2022.947572/full
_version_ 1811333540731682816
author Reine U. Protacio
Mari K. Davidson
Wayne P. Wahls
author_facet Reine U. Protacio
Mari K. Davidson
Wayne P. Wahls
author_sort Reine U. Protacio
collection DOAJ
description Meiosis is an essential component of the sexual life cycle in eukaryotes. The independent assortment of chromosomes in meiosis increases genetic diversity at the level of whole chromosomes and meiotic recombination increases genetic diversity within chromosomes. The resulting variability fuels evolution. Interestingly, global mapping of recombination in diverse taxa revealed dramatic changes in its frequency distribution between closely related species, subspecies, and even isolated populations of the same species. New insight into mechanisms for these evolutionarily rapid changes has come from analyses of environmentally induced plasticity of recombination in fission yeast. Many different DNA sites, and where identified their binding/activator proteins, control the positioning of recombination at hotspots. Each different class of hotspots functions as an independently controlled rheostat that modulates rates of recombination over a broad dynamic range in response to changing conditions. Together, this independent modulation can rapidly and dramatically alter the global frequency distribution of recombination. This process likely contributes substantially to (i.e., can largely explain) evolutionarily rapid, Prdm9-independent changes in the recombination landscape. Moreover, the precise control mechanisms allow cells to dynamically favor or disfavor newly arising combinations of linked alleles in response to changing extracellular and intracellular conditions, which has striking implications for the impacts of meiotic recombination on evolution.
first_indexed 2024-04-13T16:54:25Z
format Article
id doaj.art-e471a4a6359e4dc1be23aa326740a981
institution Directory Open Access Journal
issn 1664-8021
language English
last_indexed 2024-04-13T16:54:25Z
publishDate 2022-06-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Genetics
spelling doaj.art-e471a4a6359e4dc1be23aa326740a9812022-12-22T02:38:52ZengFrontiers Media S.A.Frontiers in Genetics1664-80212022-06-011310.3389/fgene.2022.947572947572Adaptive Control of the Meiotic Recombination Landscape by DNA Site-dependent Hotspots With Implications for EvolutionReine U. ProtacioMari K. DavidsonWayne P. WahlsMeiosis is an essential component of the sexual life cycle in eukaryotes. The independent assortment of chromosomes in meiosis increases genetic diversity at the level of whole chromosomes and meiotic recombination increases genetic diversity within chromosomes. The resulting variability fuels evolution. Interestingly, global mapping of recombination in diverse taxa revealed dramatic changes in its frequency distribution between closely related species, subspecies, and even isolated populations of the same species. New insight into mechanisms for these evolutionarily rapid changes has come from analyses of environmentally induced plasticity of recombination in fission yeast. Many different DNA sites, and where identified their binding/activator proteins, control the positioning of recombination at hotspots. Each different class of hotspots functions as an independently controlled rheostat that modulates rates of recombination over a broad dynamic range in response to changing conditions. Together, this independent modulation can rapidly and dramatically alter the global frequency distribution of recombination. This process likely contributes substantially to (i.e., can largely explain) evolutionarily rapid, Prdm9-independent changes in the recombination landscape. Moreover, the precise control mechanisms allow cells to dynamically favor or disfavor newly arising combinations of linked alleles in response to changing extracellular and intracellular conditions, which has striking implications for the impacts of meiotic recombination on evolution.https://www.frontiersin.org/articles/10.3389/fgene.2022.947572/fullmeiosisrecombination evolutionrecombination hotspotlinkage disequiblibriumgenetic mappingevolution
spellingShingle Reine U. Protacio
Mari K. Davidson
Wayne P. Wahls
Adaptive Control of the Meiotic Recombination Landscape by DNA Site-dependent Hotspots With Implications for Evolution
Frontiers in Genetics
meiosis
recombination evolution
recombination hotspot
linkage disequiblibrium
genetic mapping
evolution
title Adaptive Control of the Meiotic Recombination Landscape by DNA Site-dependent Hotspots With Implications for Evolution
title_full Adaptive Control of the Meiotic Recombination Landscape by DNA Site-dependent Hotspots With Implications for Evolution
title_fullStr Adaptive Control of the Meiotic Recombination Landscape by DNA Site-dependent Hotspots With Implications for Evolution
title_full_unstemmed Adaptive Control of the Meiotic Recombination Landscape by DNA Site-dependent Hotspots With Implications for Evolution
title_short Adaptive Control of the Meiotic Recombination Landscape by DNA Site-dependent Hotspots With Implications for Evolution
title_sort adaptive control of the meiotic recombination landscape by dna site dependent hotspots with implications for evolution
topic meiosis
recombination evolution
recombination hotspot
linkage disequiblibrium
genetic mapping
evolution
url https://www.frontiersin.org/articles/10.3389/fgene.2022.947572/full
work_keys_str_mv AT reineuprotacio adaptivecontrolofthemeioticrecombinationlandscapebydnasitedependenthotspotswithimplicationsforevolution
AT marikdavidson adaptivecontrolofthemeioticrecombinationlandscapebydnasitedependenthotspotswithimplicationsforevolution
AT waynepwahls adaptivecontrolofthemeioticrecombinationlandscapebydnasitedependenthotspotswithimplicationsforevolution