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Endogenous retroviruses drive species-specific germline transcriptomes in mammals
Gene regulation in the germline ensures the production of high-quality gametes, long-term maintenance of the species, and speciation. Male germline transcriptomes undergo dynamic changes after the mitosis-to-meiosis transition and have been subject to evolutionary divergence among mammals. However,...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246630/ https://www.ncbi.nlm.nih.gov/pubmed/32895553 http://dx.doi.org/10.1038/s41594-020-0487-4 |
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author | Sakashita, Akihiko Maezawa, So Takahashi, Kazuki Alavattam, Kris G. Yukawa, Masashi Hu, Yueh-Chiang Kojima, Shohei Parrish, Nicholas F. Barski, Artem Pavlicev, Mihaela Namekawa, Satoshi H. |
author_facet | Sakashita, Akihiko Maezawa, So Takahashi, Kazuki Alavattam, Kris G. Yukawa, Masashi Hu, Yueh-Chiang Kojima, Shohei Parrish, Nicholas F. Barski, Artem Pavlicev, Mihaela Namekawa, Satoshi H. |
author_sort | Sakashita, Akihiko |
collection | PubMed |
description | Gene regulation in the germline ensures the production of high-quality gametes, long-term maintenance of the species, and speciation. Male germline transcriptomes undergo dynamic changes after the mitosis-to-meiosis transition and have been subject to evolutionary divergence among mammals. However, the mechanisms underlying germline regulatory divergence remain undetermined. Here, we show that endogenous retroviruses (ERVs) influence species-specific germline transcriptomes. After the mitosis-to-meiosis transition in male mice, specific ERVs function as active enhancers to drive germline genes, including a mouse-specific gene set, and bear binding motifs for critical regulators of spermatogenesis such as A-MYB. This raises the possibility that a genome-wide transposition of ERVs rewired germline gene expression in a species-specific manner. Of note, independently evolved ERVs are associated with the expression of human-specific germline genes, demonstrating the prevalence of ERV-driven mechanisms in mammals. Together, we propose that ERVs fine-tune species-specific transcriptomes in the mammalian germline. |
format | Online Article Text |
id | pubmed-8246630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-82466302021-07-01 Endogenous retroviruses drive species-specific germline transcriptomes in mammals Sakashita, Akihiko Maezawa, So Takahashi, Kazuki Alavattam, Kris G. Yukawa, Masashi Hu, Yueh-Chiang Kojima, Shohei Parrish, Nicholas F. Barski, Artem Pavlicev, Mihaela Namekawa, Satoshi H. Nat Struct Mol Biol Article Gene regulation in the germline ensures the production of high-quality gametes, long-term maintenance of the species, and speciation. Male germline transcriptomes undergo dynamic changes after the mitosis-to-meiosis transition and have been subject to evolutionary divergence among mammals. However, the mechanisms underlying germline regulatory divergence remain undetermined. Here, we show that endogenous retroviruses (ERVs) influence species-specific germline transcriptomes. After the mitosis-to-meiosis transition in male mice, specific ERVs function as active enhancers to drive germline genes, including a mouse-specific gene set, and bear binding motifs for critical regulators of spermatogenesis such as A-MYB. This raises the possibility that a genome-wide transposition of ERVs rewired germline gene expression in a species-specific manner. Of note, independently evolved ERVs are associated with the expression of human-specific germline genes, demonstrating the prevalence of ERV-driven mechanisms in mammals. Together, we propose that ERVs fine-tune species-specific transcriptomes in the mammalian germline. 2020-09-07 2020-10 /pmc/articles/PMC8246630/ /pubmed/32895553 http://dx.doi.org/10.1038/s41594-020-0487-4 Text en http://www.nature.com/authors/editorial_policies/license.html#termsUsers may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Sakashita, Akihiko Maezawa, So Takahashi, Kazuki Alavattam, Kris G. Yukawa, Masashi Hu, Yueh-Chiang Kojima, Shohei Parrish, Nicholas F. Barski, Artem Pavlicev, Mihaela Namekawa, Satoshi H. Endogenous retroviruses drive species-specific germline transcriptomes in mammals |
title | Endogenous retroviruses drive species-specific germline transcriptomes in mammals |
title_full | Endogenous retroviruses drive species-specific germline transcriptomes in mammals |
title_fullStr | Endogenous retroviruses drive species-specific germline transcriptomes in mammals |
title_full_unstemmed | Endogenous retroviruses drive species-specific germline transcriptomes in mammals |
title_short | Endogenous retroviruses drive species-specific germline transcriptomes in mammals |
title_sort | endogenous retroviruses drive species-specific germline transcriptomes in mammals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246630/ https://www.ncbi.nlm.nih.gov/pubmed/32895553 http://dx.doi.org/10.1038/s41594-020-0487-4 |
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