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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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Autores principales: Liebl, Andrea L., Wesner, Jeff S., Russell, Andrew F., Schrey, Aaron W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8177507/
https://www.ncbi.nlm.nih.gov/pubmed/34086730
http://dx.doi.org/10.1371/journal.pone.0252227
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author Liebl, Andrea L.
Wesner, Jeff S.
Russell, Andrew F.
Schrey, Aaron W.
author_facet Liebl, Andrea L.
Wesner, Jeff S.
Russell, Andrew F.
Schrey, Aaron W.
author_sort Liebl, Andrea L.
collection PubMed
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.
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spelling pubmed-81775072021-06-07 Methylation patterns at fledging predict delayed dispersal in a cooperatively breeding bird Liebl, Andrea L. Wesner, Jeff S. Russell, Andrew F. Schrey, Aaron W. PLoS One Research Article 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. Public Library of Science 2021-06-04 /pmc/articles/PMC8177507/ /pubmed/34086730 http://dx.doi.org/10.1371/journal.pone.0252227 Text en © 2021 Liebl et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Liebl, Andrea L.
Wesner, Jeff S.
Russell, Andrew F.
Schrey, Aaron W.
Methylation patterns at fledging predict delayed dispersal in a cooperatively breeding bird
title 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_short 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
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8177507/
https://www.ncbi.nlm.nih.gov/pubmed/34086730
http://dx.doi.org/10.1371/journal.pone.0252227
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