Cargando…

Y-chromosomes can constrain adaptive evolution via epistatic interactions with other chromosomes

BACKGROUND: Variation in the non-coding regions of Y-chromosomes have been shown to influence gene regulation throughout the genome in some systems; a phenomenon termed Y-linked regulatory variation (YRV). This type of sex-specific genetic variance could have important implications for the evolution...

Descripción completa

Detalles Bibliográficos
Autores principales: Kutch, Ian C., Fedorka, Kenneth M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307184/
https://www.ncbi.nlm.nih.gov/pubmed/30587105
http://dx.doi.org/10.1186/s12862-018-1327-6
_version_ 1783382948217618432
author Kutch, Ian C.
Fedorka, Kenneth M.
author_facet Kutch, Ian C.
Fedorka, Kenneth M.
author_sort Kutch, Ian C.
collection PubMed
description BACKGROUND: Variation in the non-coding regions of Y-chromosomes have been shown to influence gene regulation throughout the genome in some systems; a phenomenon termed Y-linked regulatory variation (YRV). This type of sex-specific genetic variance could have important implications for the evolution of male and female traits. If YRV contributes to the additive genetic variation of an autosomally coded trait shared between the sexes (e.g. body size), then selection could facilitate sexually dimorphic evolution via the Y-chromosome. In contrast, if YRV is entirely non-additive (i.e. interacts epistatically with other chromosomes), then Y-chromosomes could constrain trait evolution in both sexes whenever they are selected for the same trait value. The ability for this phenomenon to influence such fundamental evolutionary dynamics remains unexplored. RESULTS: Here we address the evolutionary contribution of Y-linked variance by selecting for improved male geotaxis in populations possessing multiple Y-chromosomes (i.e. possessed Y-linked additive and/or epistatic variation) or a single Y-chromosome variant (i.e. possessed no Y-linked variation). We found that males from populations possessing Y-linked variation did not significantly respond to selection; however, males from populations with no Y-linked variation did respond. These patterns suggest the presence of a large quantity of Y-linked epistatic variance in the multi-Y population that dramatically slowed its response. CONCLUSIONS: Our results imply that YRV is unlikely to facilitate the evolution of sexually dimorphic traits (at least for the trait examined here), but can interfere with the rate of trait evolution in both males and females. This result could have real biological implications as it suggests that YRV can affect how quickly a population responds to new selective pressures (e.g. invasive species, novel pathogens, or climate change). Considering that YRV influences hundreds of genes and is likely typical of other independently-evolved hemizygous chromosomes, YRV-like phenomena may represent common and significant costs to hemizygous sex determination.
format Online
Article
Text
id pubmed-6307184
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-63071842019-01-02 Y-chromosomes can constrain adaptive evolution via epistatic interactions with other chromosomes Kutch, Ian C. Fedorka, Kenneth M. BMC Evol Biol Research Article BACKGROUND: Variation in the non-coding regions of Y-chromosomes have been shown to influence gene regulation throughout the genome in some systems; a phenomenon termed Y-linked regulatory variation (YRV). This type of sex-specific genetic variance could have important implications for the evolution of male and female traits. If YRV contributes to the additive genetic variation of an autosomally coded trait shared between the sexes (e.g. body size), then selection could facilitate sexually dimorphic evolution via the Y-chromosome. In contrast, if YRV is entirely non-additive (i.e. interacts epistatically with other chromosomes), then Y-chromosomes could constrain trait evolution in both sexes whenever they are selected for the same trait value. The ability for this phenomenon to influence such fundamental evolutionary dynamics remains unexplored. RESULTS: Here we address the evolutionary contribution of Y-linked variance by selecting for improved male geotaxis in populations possessing multiple Y-chromosomes (i.e. possessed Y-linked additive and/or epistatic variation) or a single Y-chromosome variant (i.e. possessed no Y-linked variation). We found that males from populations possessing Y-linked variation did not significantly respond to selection; however, males from populations with no Y-linked variation did respond. These patterns suggest the presence of a large quantity of Y-linked epistatic variance in the multi-Y population that dramatically slowed its response. CONCLUSIONS: Our results imply that YRV is unlikely to facilitate the evolution of sexually dimorphic traits (at least for the trait examined here), but can interfere with the rate of trait evolution in both males and females. This result could have real biological implications as it suggests that YRV can affect how quickly a population responds to new selective pressures (e.g. invasive species, novel pathogens, or climate change). Considering that YRV influences hundreds of genes and is likely typical of other independently-evolved hemizygous chromosomes, YRV-like phenomena may represent common and significant costs to hemizygous sex determination. BioMed Central 2018-12-27 /pmc/articles/PMC6307184/ /pubmed/30587105 http://dx.doi.org/10.1186/s12862-018-1327-6 Text en © The Author(s). 2018 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
Kutch, Ian C.
Fedorka, Kenneth M.
Y-chromosomes can constrain adaptive evolution via epistatic interactions with other chromosomes
title Y-chromosomes can constrain adaptive evolution via epistatic interactions with other chromosomes
title_full Y-chromosomes can constrain adaptive evolution via epistatic interactions with other chromosomes
title_fullStr Y-chromosomes can constrain adaptive evolution via epistatic interactions with other chromosomes
title_full_unstemmed Y-chromosomes can constrain adaptive evolution via epistatic interactions with other chromosomes
title_short Y-chromosomes can constrain adaptive evolution via epistatic interactions with other chromosomes
title_sort y-chromosomes can constrain adaptive evolution via epistatic interactions with other chromosomes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307184/
https://www.ncbi.nlm.nih.gov/pubmed/30587105
http://dx.doi.org/10.1186/s12862-018-1327-6
work_keys_str_mv AT kutchianc ychromosomescanconstrainadaptiveevolutionviaepistaticinteractionswithotherchromosomes
AT fedorkakennethm ychromosomescanconstrainadaptiveevolutionviaepistaticinteractionswithotherchromosomes