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The m6A methylation regulates gonadal sex differentiation in chicken embryo

BACKGROUND: As a ubiquitous reversible epigenetic RNA modification, N6-methyladenosine (m6A) plays crucial regulatory roles in multiple biological pathways. However, its functional mechanisms in sex determination and differentiation during gonadal development of chicken embryos are not clear. Theref...

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Autores principales: Li, Jianbo, Zhang, Xiuan, Wang, Xiqiong, Sun, Congjiao, Zheng, Jiangxia, Li, Junying, Yi, Guoqiang, Yang, Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9115958/
https://www.ncbi.nlm.nih.gov/pubmed/35581635
http://dx.doi.org/10.1186/s40104-022-00710-6
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author Li, Jianbo
Zhang, Xiuan
Wang, Xiqiong
Sun, Congjiao
Zheng, Jiangxia
Li, Junying
Yi, Guoqiang
Yang, Ning
author_facet Li, Jianbo
Zhang, Xiuan
Wang, Xiqiong
Sun, Congjiao
Zheng, Jiangxia
Li, Junying
Yi, Guoqiang
Yang, Ning
author_sort Li, Jianbo
collection PubMed
description BACKGROUND: As a ubiquitous reversible epigenetic RNA modification, N6-methyladenosine (m6A) plays crucial regulatory roles in multiple biological pathways. However, its functional mechanisms in sex determination and differentiation during gonadal development of chicken embryos are not clear. Therefore, we established a transcriptome-wide m6A map in the female and male chicken left gonads of embryonic day 7 (E7) by methylated RNA immunoprecipitation sequencing (MeRIP-seq) to offer insight into the landscape of m6A methylation and investigate the post-transcriptional modification underlying gonadal differentiation. RESULTS: The chicken embryonic gonadal transcriptome was extensively methylated. We found 15,191 and 16,111 m6A peaks in the female and male left gonads, respectively, which were mainly enriched in the coding sequence (CDS) and stop codon. Among these m6A peaks, we identified that 1013 and 751 were hypermethylated in females and males, respectively. These differential peaks covered 281 and 327 genes, such as BMP2, SMAD2, SOX9 and CYP19A1, which were primarily associated with development, morphogenesis and sex differentiation by functional enrichment. Further analysis revealed that the m6A methylation level was positively correlated with gene expression abundance. Furthermore, we found that YTHDC2 could regulate the expression of sex-related genes, especially HEMGN and SOX9, in male mesonephros/gonad mingle cells, which was verified by in vitro experiments, suggesting a regulatory role of m6A methylation in chicken gonad differentiation. CONCLUSIONS: This work provided a comprehensive m6A methylation profile of chicken embryonic gonads and revealed YTHDC2 as a key regulator responsible for sex differentiation. Our results contribute to a better understanding of epigenetic factors involved in chicken sex determination and differentiation and to promoting the future development of sex manipulation in poultry industry. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40104-022-00710-6.
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spelling pubmed-91159582022-05-19 The m6A methylation regulates gonadal sex differentiation in chicken embryo Li, Jianbo Zhang, Xiuan Wang, Xiqiong Sun, Congjiao Zheng, Jiangxia Li, Junying Yi, Guoqiang Yang, Ning J Anim Sci Biotechnol Research BACKGROUND: As a ubiquitous reversible epigenetic RNA modification, N6-methyladenosine (m6A) plays crucial regulatory roles in multiple biological pathways. However, its functional mechanisms in sex determination and differentiation during gonadal development of chicken embryos are not clear. Therefore, we established a transcriptome-wide m6A map in the female and male chicken left gonads of embryonic day 7 (E7) by methylated RNA immunoprecipitation sequencing (MeRIP-seq) to offer insight into the landscape of m6A methylation and investigate the post-transcriptional modification underlying gonadal differentiation. RESULTS: The chicken embryonic gonadal transcriptome was extensively methylated. We found 15,191 and 16,111 m6A peaks in the female and male left gonads, respectively, which were mainly enriched in the coding sequence (CDS) and stop codon. Among these m6A peaks, we identified that 1013 and 751 were hypermethylated in females and males, respectively. These differential peaks covered 281 and 327 genes, such as BMP2, SMAD2, SOX9 and CYP19A1, which were primarily associated with development, morphogenesis and sex differentiation by functional enrichment. Further analysis revealed that the m6A methylation level was positively correlated with gene expression abundance. Furthermore, we found that YTHDC2 could regulate the expression of sex-related genes, especially HEMGN and SOX9, in male mesonephros/gonad mingle cells, which was verified by in vitro experiments, suggesting a regulatory role of m6A methylation in chicken gonad differentiation. CONCLUSIONS: This work provided a comprehensive m6A methylation profile of chicken embryonic gonads and revealed YTHDC2 as a key regulator responsible for sex differentiation. Our results contribute to a better understanding of epigenetic factors involved in chicken sex determination and differentiation and to promoting the future development of sex manipulation in poultry industry. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40104-022-00710-6. BioMed Central 2022-05-18 /pmc/articles/PMC9115958/ /pubmed/35581635 http://dx.doi.org/10.1186/s40104-022-00710-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Li, Jianbo
Zhang, Xiuan
Wang, Xiqiong
Sun, Congjiao
Zheng, Jiangxia
Li, Junying
Yi, Guoqiang
Yang, Ning
The m6A methylation regulates gonadal sex differentiation in chicken embryo
title The m6A methylation regulates gonadal sex differentiation in chicken embryo
title_full The m6A methylation regulates gonadal sex differentiation in chicken embryo
title_fullStr The m6A methylation regulates gonadal sex differentiation in chicken embryo
title_full_unstemmed The m6A methylation regulates gonadal sex differentiation in chicken embryo
title_short The m6A methylation regulates gonadal sex differentiation in chicken embryo
title_sort m6a methylation regulates gonadal sex differentiation in chicken embryo
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9115958/
https://www.ncbi.nlm.nih.gov/pubmed/35581635
http://dx.doi.org/10.1186/s40104-022-00710-6
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