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Genomic imprinting-like monoallelic paternal expression determines sex of channel catfish
The X and Y chromosomes of channel catfish have the same gene contents. Here, we report allelic hypermethylation of the X chromosome within the sex determination region (SDR). Accordingly, the X-borne hydin-1 gene was silenced, whereas the Y-borne hydin-1 gene was expressed, making monoallelic expre...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9770954/ https://www.ncbi.nlm.nih.gov/pubmed/36542716 http://dx.doi.org/10.1126/sciadv.adc8786 |
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author | Wang, Wenwen Yang, Yujia Tan, Suxu Zhou, Tao Liu, Yang Tian, Changxu Bao, Lisui Xing, De Su, Baofeng Wang, Jinhai Zhang, Yu Liu, Shikai Shi, Huitong Gao, Dongya Dunham, Rex Liu, Zhanjiang |
author_facet | Wang, Wenwen Yang, Yujia Tan, Suxu Zhou, Tao Liu, Yang Tian, Changxu Bao, Lisui Xing, De Su, Baofeng Wang, Jinhai Zhang, Yu Liu, Shikai Shi, Huitong Gao, Dongya Dunham, Rex Liu, Zhanjiang |
author_sort | Wang, Wenwen |
collection | PubMed |
description | The X and Y chromosomes of channel catfish have the same gene contents. Here, we report allelic hypermethylation of the X chromosome within the sex determination region (SDR). Accordingly, the X-borne hydin-1 gene was silenced, whereas the Y-borne hydin-1 gene was expressed, making monoallelic expression of hydin-1 responsible for sex determination, much like genomic imprinting. Treatment with a methylation inhibitor, 5-aza-dC, erased the epigenetic marks within the SDR and caused sex reversal of genetic females into phenotypic males. After the treatment, hydin-1 and six other genes related to cell cycle control and proliferative growth were up-regulated, while three genes related to female sex differentiation were down-regulated in genetic females, providing additional support for epigenetic sex determination in catfish. This mechanism of sex determination provides insights into the plasticity of genetic sex determination in lower vertebrates and its connection with temperature sex determination where DNA methylation is broadly involved. |
format | Online Article Text |
id | pubmed-9770954 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-97709542022-12-28 Genomic imprinting-like monoallelic paternal expression determines sex of channel catfish Wang, Wenwen Yang, Yujia Tan, Suxu Zhou, Tao Liu, Yang Tian, Changxu Bao, Lisui Xing, De Su, Baofeng Wang, Jinhai Zhang, Yu Liu, Shikai Shi, Huitong Gao, Dongya Dunham, Rex Liu, Zhanjiang Sci Adv Biomedicine and Life Sciences The X and Y chromosomes of channel catfish have the same gene contents. Here, we report allelic hypermethylation of the X chromosome within the sex determination region (SDR). Accordingly, the X-borne hydin-1 gene was silenced, whereas the Y-borne hydin-1 gene was expressed, making monoallelic expression of hydin-1 responsible for sex determination, much like genomic imprinting. Treatment with a methylation inhibitor, 5-aza-dC, erased the epigenetic marks within the SDR and caused sex reversal of genetic females into phenotypic males. After the treatment, hydin-1 and six other genes related to cell cycle control and proliferative growth were up-regulated, while three genes related to female sex differentiation were down-regulated in genetic females, providing additional support for epigenetic sex determination in catfish. This mechanism of sex determination provides insights into the plasticity of genetic sex determination in lower vertebrates and its connection with temperature sex determination where DNA methylation is broadly involved. American Association for the Advancement of Science 2022-12-21 /pmc/articles/PMC9770954/ /pubmed/36542716 http://dx.doi.org/10.1126/sciadv.adc8786 Text en Copyright © 2022 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). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://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 | Biomedicine and Life Sciences Wang, Wenwen Yang, Yujia Tan, Suxu Zhou, Tao Liu, Yang Tian, Changxu Bao, Lisui Xing, De Su, Baofeng Wang, Jinhai Zhang, Yu Liu, Shikai Shi, Huitong Gao, Dongya Dunham, Rex Liu, Zhanjiang Genomic imprinting-like monoallelic paternal expression determines sex of channel catfish |
title | Genomic imprinting-like monoallelic paternal expression determines sex of channel catfish |
title_full | Genomic imprinting-like monoallelic paternal expression determines sex of channel catfish |
title_fullStr | Genomic imprinting-like monoallelic paternal expression determines sex of channel catfish |
title_full_unstemmed | Genomic imprinting-like monoallelic paternal expression determines sex of channel catfish |
title_short | Genomic imprinting-like monoallelic paternal expression determines sex of channel catfish |
title_sort | genomic imprinting-like monoallelic paternal expression determines sex of channel catfish |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9770954/ https://www.ncbi.nlm.nih.gov/pubmed/36542716 http://dx.doi.org/10.1126/sciadv.adc8786 |
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