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Nutrient restriction synergizes with retinoic acid to induce mammalian meiotic initiation in vitro
The molecular machinery and chromosome structures carrying out meiosis are frequently conserved from yeast to mammals. However, signals initiating meiosis appear divergent: while nutrient restriction induces meiosis in the yeast system, retinoic acid (RA) and its target Stra8 have been shown to be n...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7979727/ https://www.ncbi.nlm.nih.gov/pubmed/33741948 http://dx.doi.org/10.1038/s41467-021-22021-6 |
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author | Zhang, Xiaoyu Gunewardena, Sumedha Wang, Ning |
author_facet | Zhang, Xiaoyu Gunewardena, Sumedha Wang, Ning |
author_sort | Zhang, Xiaoyu |
collection | PubMed |
description | The molecular machinery and chromosome structures carrying out meiosis are frequently conserved from yeast to mammals. However, signals initiating meiosis appear divergent: while nutrient restriction induces meiosis in the yeast system, retinoic acid (RA) and its target Stra8 have been shown to be necessary but not sufficient to induce meiotic initiation in mammalian germ cells. Here, we use primary culture of mouse undifferentiated spermatogonia without the support of gonadal somatic cells to show that nutrient restriction in combination with RA is sufficient to induce Stra8- and Spo11-dependent meiotic gene and chromosome programs that recapitulate the transcriptomic and cytologic features of in vivo meiosis. We demonstrate that neither nutrient restriction nor RA alone exerts these effects. Moreover, we identify a distinctive network of 11 nutrient restriction-upregulated transcription factor genes, which are associated with early meiosis in vivo and whose expression does not require RA. Our study proposes a conserved model, in which nutrient restriction induces meiotic initiation by upregulating key transcription factor genes for the meiotic gene program and provides an in vitro platform for meiotic induction that could facilitate research and haploid gamete production. |
format | Online Article Text |
id | pubmed-7979727 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79797272021-04-16 Nutrient restriction synergizes with retinoic acid to induce mammalian meiotic initiation in vitro Zhang, Xiaoyu Gunewardena, Sumedha Wang, Ning Nat Commun Article The molecular machinery and chromosome structures carrying out meiosis are frequently conserved from yeast to mammals. However, signals initiating meiosis appear divergent: while nutrient restriction induces meiosis in the yeast system, retinoic acid (RA) and its target Stra8 have been shown to be necessary but not sufficient to induce meiotic initiation in mammalian germ cells. Here, we use primary culture of mouse undifferentiated spermatogonia without the support of gonadal somatic cells to show that nutrient restriction in combination with RA is sufficient to induce Stra8- and Spo11-dependent meiotic gene and chromosome programs that recapitulate the transcriptomic and cytologic features of in vivo meiosis. We demonstrate that neither nutrient restriction nor RA alone exerts these effects. Moreover, we identify a distinctive network of 11 nutrient restriction-upregulated transcription factor genes, which are associated with early meiosis in vivo and whose expression does not require RA. Our study proposes a conserved model, in which nutrient restriction induces meiotic initiation by upregulating key transcription factor genes for the meiotic gene program and provides an in vitro platform for meiotic induction that could facilitate research and haploid gamete production. Nature Publishing Group UK 2021-03-19 /pmc/articles/PMC7979727/ /pubmed/33741948 http://dx.doi.org/10.1038/s41467-021-22021-6 Text en © The Author(s) 2021 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zhang, Xiaoyu Gunewardena, Sumedha Wang, Ning Nutrient restriction synergizes with retinoic acid to induce mammalian meiotic initiation in vitro |
title | Nutrient restriction synergizes with retinoic acid to induce mammalian meiotic initiation in vitro |
title_full | Nutrient restriction synergizes with retinoic acid to induce mammalian meiotic initiation in vitro |
title_fullStr | Nutrient restriction synergizes with retinoic acid to induce mammalian meiotic initiation in vitro |
title_full_unstemmed | Nutrient restriction synergizes with retinoic acid to induce mammalian meiotic initiation in vitro |
title_short | Nutrient restriction synergizes with retinoic acid to induce mammalian meiotic initiation in vitro |
title_sort | nutrient restriction synergizes with retinoic acid to induce mammalian meiotic initiation in vitro |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7979727/ https://www.ncbi.nlm.nih.gov/pubmed/33741948 http://dx.doi.org/10.1038/s41467-021-22021-6 |
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