Methylation patterns at fledging predict delayed dispersal in a cooperatively breeding bird.

Individuals may delay dispersing from their natal habitat, even after maturation to adulthood. Such delays can have broad consequences from determining population structure to allowing an individual to gain indirect fitness by helping parents rear future offspring. Dispersal in species that use dela...

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Main Authors: Andrea L Liebl, Jeff S Wesner, Andrew F Russell, Aaron W Schrey
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0252227
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spelling doaj-459717934aa6405081ee00a5a6d5a3a32021-06-10T04:32:46ZengPublic Library of Science (PLoS)PLoS ONE1932-62032021-01-01166e025222710.1371/journal.pone.0252227Methylation patterns at fledging predict delayed dispersal in a cooperatively breeding bird.Andrea L LieblJeff S WesnerAndrew F RussellAaron W SchreyIndividuals may delay dispersing from their natal habitat, even after maturation to adulthood. Such delays can have broad consequences from determining population structure to allowing an individual to gain indirect fitness by helping parents rear future offspring. Dispersal in species that use delayed dispersal is largely thought to be opportunistic; however, how individuals, particularly inexperienced juveniles, assess their environments to determine the appropriate time to disperse is unknown. One relatively unexplored possibility is that dispersal decisions are the result of epigenetic mechanisms interacting between a genome and environment during development to generate variable dispersive phenotypes. Here, we tested this using epiRADseq to compare genome-wide levels of DNA methylation of blood in cooperatively breeding chestnut-crowned babblers (Pomatostomus ruficeps). We measured dispersive and philopatric individuals at hatching, before fledging, and at 1 year (following when first year dispersal decisions would be made). We found that individuals that dispersed in their first year had a reduced proportion of methylated loci than philopatric individuals before fledging, but not at hatching or as adults. Further, individuals that dispersed in the first year had a greater number of loci change methylation state (i.e. gain or lose) between hatching and fledging. The existence and timing of these changes indicate some influence of development on epigenetic changes that may influence dispersal behavior. However, further work needs to be done to address exactly how developmental environments may be associated with dispersal decisions and which loci in particular are manipulated to generate such changes.https://doi.org/10.1371/journal.pone.0252227
collection DOAJ
language English
format Article
sources DOAJ
author Andrea L Liebl
Jeff S Wesner
Andrew F Russell
Aaron W Schrey
spellingShingle Andrea L Liebl
Jeff S Wesner
Andrew F Russell
Aaron W Schrey
Methylation patterns at fledging predict delayed dispersal in a cooperatively breeding bird.
PLoS ONE
author_facet Andrea L Liebl
Jeff S Wesner
Andrew F Russell
Aaron W Schrey
author_sort Andrea L Liebl
title Methylation patterns at fledging predict delayed dispersal in a cooperatively breeding bird.
title_short Methylation patterns at fledging predict delayed dispersal in a cooperatively breeding bird.
title_full Methylation patterns at fledging predict delayed dispersal in a cooperatively breeding bird.
title_fullStr Methylation patterns at fledging predict delayed dispersal in a cooperatively breeding bird.
title_full_unstemmed Methylation patterns at fledging predict delayed dispersal in a cooperatively breeding bird.
title_sort methylation patterns at fledging predict delayed dispersal in a cooperatively breeding bird.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2021-01-01
description Individuals may delay dispersing from their natal habitat, even after maturation to adulthood. Such delays can have broad consequences from determining population structure to allowing an individual to gain indirect fitness by helping parents rear future offspring. Dispersal in species that use delayed dispersal is largely thought to be opportunistic; however, how individuals, particularly inexperienced juveniles, assess their environments to determine the appropriate time to disperse is unknown. One relatively unexplored possibility is that dispersal decisions are the result of epigenetic mechanisms interacting between a genome and environment during development to generate variable dispersive phenotypes. Here, we tested this using epiRADseq to compare genome-wide levels of DNA methylation of blood in cooperatively breeding chestnut-crowned babblers (Pomatostomus ruficeps). We measured dispersive and philopatric individuals at hatching, before fledging, and at 1 year (following when first year dispersal decisions would be made). We found that individuals that dispersed in their first year had a reduced proportion of methylated loci than philopatric individuals before fledging, but not at hatching or as adults. Further, individuals that dispersed in the first year had a greater number of loci change methylation state (i.e. gain or lose) between hatching and fledging. The existence and timing of these changes indicate some influence of development on epigenetic changes that may influence dispersal behavior. However, further work needs to be done to address exactly how developmental environments may be associated with dispersal decisions and which loci in particular are manipulated to generate such changes.
url https://doi.org/10.1371/journal.pone.0252227
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