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DNA methylation reprogramming, TE derepression, and postzygotic isolation of nascent animal species

The genomic shock hypothesis stipulates that the stress associated with divergent genome admixture can cause transposable element (TE) derepression, which could act as a postzygotic isolation mechanism. TEs affect gene structure, expression patterns, and chromosome organization and may have deleteri...

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Autores principales: Laporte, M., Le Luyer, J., Rougeux, C., Dion-Côté, A.-M., Krick, M., Bernatchez, L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6795504/
https://www.ncbi.nlm.nih.gov/pubmed/31663013
http://dx.doi.org/10.1126/sciadv.aaw1644
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author Laporte, M.
Le Luyer, J.
Rougeux, C.
Dion-Côté, A.-M.
Krick, M.
Bernatchez, L.
author_facet Laporte, M.
Le Luyer, J.
Rougeux, C.
Dion-Côté, A.-M.
Krick, M.
Bernatchez, L.
author_sort Laporte, M.
collection PubMed
description The genomic shock hypothesis stipulates that the stress associated with divergent genome admixture can cause transposable element (TE) derepression, which could act as a postzygotic isolation mechanism. TEs affect gene structure, expression patterns, and chromosome organization and may have deleterious consequences when released. For these reasons, they are silenced by heterochromatin formation, which includes DNA methylation. Here, we show that a significant proportion of TEs are differentially methylated between the “dwarf” (limnetic) and the “normal” (benthic) whitefish, two nascent species that diverged some 15,000 generations ago within the Coregonus clupeaformis species complex. Moreover, TEs are overrepresented among loci that were demethylated in hybrids, indicative of their transcriptional derepression. These results are consistent with earlier studies in this system that revealed TE transcriptional derepression causes abnormal embryonic development and death of hybrids. Hence, this supports a role of DNA methylation reprogramming and TE derepression in postzygotic isolation of nascent animal species.
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spelling pubmed-67955042019-10-29 DNA methylation reprogramming, TE derepression, and postzygotic isolation of nascent animal species Laporte, M. Le Luyer, J. Rougeux, C. Dion-Côté, A.-M. Krick, M. Bernatchez, L. Sci Adv Research Articles The genomic shock hypothesis stipulates that the stress associated with divergent genome admixture can cause transposable element (TE) derepression, which could act as a postzygotic isolation mechanism. TEs affect gene structure, expression patterns, and chromosome organization and may have deleterious consequences when released. For these reasons, they are silenced by heterochromatin formation, which includes DNA methylation. Here, we show that a significant proportion of TEs are differentially methylated between the “dwarf” (limnetic) and the “normal” (benthic) whitefish, two nascent species that diverged some 15,000 generations ago within the Coregonus clupeaformis species complex. Moreover, TEs are overrepresented among loci that were demethylated in hybrids, indicative of their transcriptional derepression. These results are consistent with earlier studies in this system that revealed TE transcriptional derepression causes abnormal embryonic development and death of hybrids. Hence, this supports a role of DNA methylation reprogramming and TE derepression in postzygotic isolation of nascent animal species. American Association for the Advancement of Science 2019-10-16 /pmc/articles/PMC6795504/ /pubmed/31663013 http://dx.doi.org/10.1126/sciadv.aaw1644 Text en Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Laporte, M.
Le Luyer, J.
Rougeux, C.
Dion-Côté, A.-M.
Krick, M.
Bernatchez, L.
DNA methylation reprogramming, TE derepression, and postzygotic isolation of nascent animal species
title DNA methylation reprogramming, TE derepression, and postzygotic isolation of nascent animal species
title_full DNA methylation reprogramming, TE derepression, and postzygotic isolation of nascent animal species
title_fullStr DNA methylation reprogramming, TE derepression, and postzygotic isolation of nascent animal species
title_full_unstemmed DNA methylation reprogramming, TE derepression, and postzygotic isolation of nascent animal species
title_short DNA methylation reprogramming, TE derepression, and postzygotic isolation of nascent animal species
title_sort dna methylation reprogramming, te derepression, and postzygotic isolation of nascent animal species
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6795504/
https://www.ncbi.nlm.nih.gov/pubmed/31663013
http://dx.doi.org/10.1126/sciadv.aaw1644
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