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Spontaneous and ART-induced large offspring syndrome: similarities and differences in DNA methylome

Large/abnormal offspring syndrome (LOS/AOS) is a congenital overgrowth syndrome reported in ruminants produced by assisted reproduction (ART-LOS) which exhibit global disruption of the epigenome and transcriptome. LOS/AOS shares phenotypes and epigenotypes with the human congenital overgrowth condit...

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Autores principales: Li, Yahan, Sena Lopes, Jordana, Coy-Fuster, Pilar, Rivera, Rocío Melissa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9586674/
https://www.ncbi.nlm.nih.gov/pubmed/35466858
http://dx.doi.org/10.1080/15592294.2022.2067938
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author Li, Yahan
Sena Lopes, Jordana
Coy-Fuster, Pilar
Rivera, Rocío Melissa
author_facet Li, Yahan
Sena Lopes, Jordana
Coy-Fuster, Pilar
Rivera, Rocío Melissa
author_sort Li, Yahan
collection PubMed
description Large/abnormal offspring syndrome (LOS/AOS) is a congenital overgrowth syndrome reported in ruminants produced by assisted reproduction (ART-LOS) which exhibit global disruption of the epigenome and transcriptome. LOS/AOS shares phenotypes and epigenotypes with the human congenital overgrowth condition Beckwith-Wiedemann syndrome. We have reported that LOS occurs spontaneously (SLOS); however, to date, no study has been conducted to determine if SLOS has the same methylome epimutations as ART-LOS. In this study, we performed whole-genome bisulphite sequencing to examine global DNA methylation in bovine SLOS and ART-LOS tissues. We observed unique patterns of global distribution of differentially methylated regions (DMRs) over different genomic contexts, such as promoters, CpG Islands, shores and shelves, as well as at repetitive sequences. In addition, we included data from two previous LOS studies to identify shared vulnerable genomic loci in LOS. Overall, we identified 320 genomic loci in LOS that have alterations in DNA methylation when compared to controls. Specifically, there are 25 highly vulnerable loci that could potentially serve as molecular markers for the diagnosis of LOS, including at the promoters of DMRT2 and TBX18, at the imprinted gene bodies of IGF2R, PRDM8, and BLCAP/NNAT, and at multiple CpG Islands. We also observed tissue-specific DNA methylation patterns between muscle and blood, and conservation of ART-induced DNA methylation changes between muscle and blood. We conclude that as ART-LOS, SLOS is an epigenetic condition. In addition, SLOS and ART-LOS share similarities in methylome epimutations.
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spelling pubmed-95866742022-10-22 Spontaneous and ART-induced large offspring syndrome: similarities and differences in DNA methylome Li, Yahan Sena Lopes, Jordana Coy-Fuster, Pilar Rivera, Rocío Melissa Epigenetics Research Paper Large/abnormal offspring syndrome (LOS/AOS) is a congenital overgrowth syndrome reported in ruminants produced by assisted reproduction (ART-LOS) which exhibit global disruption of the epigenome and transcriptome. LOS/AOS shares phenotypes and epigenotypes with the human congenital overgrowth condition Beckwith-Wiedemann syndrome. We have reported that LOS occurs spontaneously (SLOS); however, to date, no study has been conducted to determine if SLOS has the same methylome epimutations as ART-LOS. In this study, we performed whole-genome bisulphite sequencing to examine global DNA methylation in bovine SLOS and ART-LOS tissues. We observed unique patterns of global distribution of differentially methylated regions (DMRs) over different genomic contexts, such as promoters, CpG Islands, shores and shelves, as well as at repetitive sequences. In addition, we included data from two previous LOS studies to identify shared vulnerable genomic loci in LOS. Overall, we identified 320 genomic loci in LOS that have alterations in DNA methylation when compared to controls. Specifically, there are 25 highly vulnerable loci that could potentially serve as molecular markers for the diagnosis of LOS, including at the promoters of DMRT2 and TBX18, at the imprinted gene bodies of IGF2R, PRDM8, and BLCAP/NNAT, and at multiple CpG Islands. We also observed tissue-specific DNA methylation patterns between muscle and blood, and conservation of ART-induced DNA methylation changes between muscle and blood. We conclude that as ART-LOS, SLOS is an epigenetic condition. In addition, SLOS and ART-LOS share similarities in methylome epimutations. Taylor & Francis 2022-05-03 /pmc/articles/PMC9586674/ /pubmed/35466858 http://dx.doi.org/10.1080/15592294.2022.2067938 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Research Paper
Li, Yahan
Sena Lopes, Jordana
Coy-Fuster, Pilar
Rivera, Rocío Melissa
Spontaneous and ART-induced large offspring syndrome: similarities and differences in DNA methylome
title Spontaneous and ART-induced large offspring syndrome: similarities and differences in DNA methylome
title_full Spontaneous and ART-induced large offspring syndrome: similarities and differences in DNA methylome
title_fullStr Spontaneous and ART-induced large offspring syndrome: similarities and differences in DNA methylome
title_full_unstemmed Spontaneous and ART-induced large offspring syndrome: similarities and differences in DNA methylome
title_short Spontaneous and ART-induced large offspring syndrome: similarities and differences in DNA methylome
title_sort spontaneous and art-induced large offspring syndrome: similarities and differences in dna methylome
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9586674/
https://www.ncbi.nlm.nih.gov/pubmed/35466858
http://dx.doi.org/10.1080/15592294.2022.2067938
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