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Genome-wide DNA methylation differences between conservation and breeding populations of Shaoxing ducks

The genome-wide DNA methylation assay was used to analyze the difference in methylation between the breeding and conservation populations of Shaoxing ducks. The methylation level of the breeding population was higher than that of the two conservation populations, and the proportion of CG methylation...

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Autores principales: Xu, Ligen, Shi, Zhenzhen, Li, Haiying, He, Jun, Chen, Bindan, Tao, Zeng, Tian, Yong, Chen, Li, Li, Guoqin, Tao, Zhengrong, Gu, Tiantian, Xu, Wenwu, Lu, Lizhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9694084/
https://www.ncbi.nlm.nih.gov/pubmed/36439710
http://dx.doi.org/10.1016/j.heliyon.2022.e11644
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author Xu, Ligen
Shi, Zhenzhen
Li, Haiying
He, Jun
Chen, Bindan
Tao, Zeng
Tian, Yong
Chen, Li
Li, Guoqin
Tao, Zhengrong
Gu, Tiantian
Xu, Wenwu
Lu, Lizhi
author_facet Xu, Ligen
Shi, Zhenzhen
Li, Haiying
He, Jun
Chen, Bindan
Tao, Zeng
Tian, Yong
Chen, Li
Li, Guoqin
Tao, Zhengrong
Gu, Tiantian
Xu, Wenwu
Lu, Lizhi
author_sort Xu, Ligen
collection PubMed
description The genome-wide DNA methylation assay was used to analyze the difference in methylation between the breeding and conservation populations of Shaoxing ducks. The methylation level of the breeding population was higher than that of the two conservation populations, and the proportion of CG methylation sites was the largest in the three populations, most of the methylation sites were located in the exon region. There were 1247 different methylation regions in the two populations (group A and B), and 927 different methylation regions in the two groups (group A and group C). The differential methylation regions of the three groups were evenly distributed in the gene and intergene regions. GO and KEGG enrichment analysis showed that the differentially expressed genes in the A and B groups were mainly involved in synaptic and cell connections and the signaling pathways were significantly enriched in cAMP and oxytocin signaling pathways. The results showed that the group C was significantly enriched in eight signaling pathways, including the cAMP signaling pathway and long-term enhancement, compared to the group A. There were thirty-five differentially methylated genes, including CACNA1C, GRIA1, GRIA2, GABBR2, PDE10A, BRAF, GRM5, CPEB3, FMn2, GABRB2, PTK2, and CNTN1. These genes were involved in the development and ovulation of ovaries and follicles and were closely related to the excellent production performance of the breeding population. In addition, ATP2B1, ATP2B2, and other genes related to eggshell quality were identified, which can be used as molecular markers to improve eggshell quality in the future.
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spelling pubmed-96940842022-11-26 Genome-wide DNA methylation differences between conservation and breeding populations of Shaoxing ducks Xu, Ligen Shi, Zhenzhen Li, Haiying He, Jun Chen, Bindan Tao, Zeng Tian, Yong Chen, Li Li, Guoqin Tao, Zhengrong Gu, Tiantian Xu, Wenwu Lu, Lizhi Heliyon Research Article The genome-wide DNA methylation assay was used to analyze the difference in methylation between the breeding and conservation populations of Shaoxing ducks. The methylation level of the breeding population was higher than that of the two conservation populations, and the proportion of CG methylation sites was the largest in the three populations, most of the methylation sites were located in the exon region. There were 1247 different methylation regions in the two populations (group A and B), and 927 different methylation regions in the two groups (group A and group C). The differential methylation regions of the three groups were evenly distributed in the gene and intergene regions. GO and KEGG enrichment analysis showed that the differentially expressed genes in the A and B groups were mainly involved in synaptic and cell connections and the signaling pathways were significantly enriched in cAMP and oxytocin signaling pathways. The results showed that the group C was significantly enriched in eight signaling pathways, including the cAMP signaling pathway and long-term enhancement, compared to the group A. There were thirty-five differentially methylated genes, including CACNA1C, GRIA1, GRIA2, GABBR2, PDE10A, BRAF, GRM5, CPEB3, FMn2, GABRB2, PTK2, and CNTN1. These genes were involved in the development and ovulation of ovaries and follicles and were closely related to the excellent production performance of the breeding population. In addition, ATP2B1, ATP2B2, and other genes related to eggshell quality were identified, which can be used as molecular markers to improve eggshell quality in the future. Elsevier 2022-11-17 /pmc/articles/PMC9694084/ /pubmed/36439710 http://dx.doi.org/10.1016/j.heliyon.2022.e11644 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Xu, Ligen
Shi, Zhenzhen
Li, Haiying
He, Jun
Chen, Bindan
Tao, Zeng
Tian, Yong
Chen, Li
Li, Guoqin
Tao, Zhengrong
Gu, Tiantian
Xu, Wenwu
Lu, Lizhi
Genome-wide DNA methylation differences between conservation and breeding populations of Shaoxing ducks
title Genome-wide DNA methylation differences between conservation and breeding populations of Shaoxing ducks
title_full Genome-wide DNA methylation differences between conservation and breeding populations of Shaoxing ducks
title_fullStr Genome-wide DNA methylation differences between conservation and breeding populations of Shaoxing ducks
title_full_unstemmed Genome-wide DNA methylation differences between conservation and breeding populations of Shaoxing ducks
title_short Genome-wide DNA methylation differences between conservation and breeding populations of Shaoxing ducks
title_sort genome-wide dna methylation differences between conservation and breeding populations of shaoxing ducks
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9694084/
https://www.ncbi.nlm.nih.gov/pubmed/36439710
http://dx.doi.org/10.1016/j.heliyon.2022.e11644
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