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Cellular fate of intersex differentiation
Infertile ovotestis (mixture of ovary and testis) often occurs in intersex individuals under certain pathological and physiological conditions. However, how ovotestis is formed remains largely unknown. Here, we report the first comprehensive single-cell developmental atlas of the model ovotestis. We...
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/PMC8041806/ https://www.ncbi.nlm.nih.gov/pubmed/33846307 http://dx.doi.org/10.1038/s41419-021-03676-x |
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author | Wang, Xin Lai, Fengling Shang, Dantong Cheng, Yibin Lan, Tian Cheng, Hanhua Zhou, Rongjia |
author_facet | Wang, Xin Lai, Fengling Shang, Dantong Cheng, Yibin Lan, Tian Cheng, Hanhua Zhou, Rongjia |
author_sort | Wang, Xin |
collection | PubMed |
description | Infertile ovotestis (mixture of ovary and testis) often occurs in intersex individuals under certain pathological and physiological conditions. However, how ovotestis is formed remains largely unknown. Here, we report the first comprehensive single-cell developmental atlas of the model ovotestis. We provide an overview of cell identities and a roadmap of germline, niche, and stem cell development in ovotestis by cell lineage reconstruction and a uniform manifold approximation and projection. We identify common progenitors of germline stem cells with two states, which reveal their bipotential nature to differentiate into both spermatogonial stem cells and female germline stem cells. Moreover, we found that ovotestis infertility was caused by degradation of female germline cells via liquid–liquid phase separation of the proteasomes in the nucleus, and impaired histone-to-protamine replacement in spermatid differentiation. Notably, signaling pathways in gonadal niche cells and their interaction with germlines synergistically determined distinct cell fate of both male and female germlines. Overall, we reveal a cellular fate map of germline and niche cell development that shapes cell differentiation direction of ovotestis, and provide novel insights into ovotestis development. |
format | Online Article Text |
id | pubmed-8041806 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80418062021-04-28 Cellular fate of intersex differentiation Wang, Xin Lai, Fengling Shang, Dantong Cheng, Yibin Lan, Tian Cheng, Hanhua Zhou, Rongjia Cell Death Dis Article Infertile ovotestis (mixture of ovary and testis) often occurs in intersex individuals under certain pathological and physiological conditions. However, how ovotestis is formed remains largely unknown. Here, we report the first comprehensive single-cell developmental atlas of the model ovotestis. We provide an overview of cell identities and a roadmap of germline, niche, and stem cell development in ovotestis by cell lineage reconstruction and a uniform manifold approximation and projection. We identify common progenitors of germline stem cells with two states, which reveal their bipotential nature to differentiate into both spermatogonial stem cells and female germline stem cells. Moreover, we found that ovotestis infertility was caused by degradation of female germline cells via liquid–liquid phase separation of the proteasomes in the nucleus, and impaired histone-to-protamine replacement in spermatid differentiation. Notably, signaling pathways in gonadal niche cells and their interaction with germlines synergistically determined distinct cell fate of both male and female germlines. Overall, we reveal a cellular fate map of germline and niche cell development that shapes cell differentiation direction of ovotestis, and provide novel insights into ovotestis development. Nature Publishing Group UK 2021-04-12 /pmc/articles/PMC8041806/ /pubmed/33846307 http://dx.doi.org/10.1038/s41419-021-03676-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wang, Xin Lai, Fengling Shang, Dantong Cheng, Yibin Lan, Tian Cheng, Hanhua Zhou, Rongjia Cellular fate of intersex differentiation |
title | Cellular fate of intersex differentiation |
title_full | Cellular fate of intersex differentiation |
title_fullStr | Cellular fate of intersex differentiation |
title_full_unstemmed | Cellular fate of intersex differentiation |
title_short | Cellular fate of intersex differentiation |
title_sort | cellular fate of intersex differentiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8041806/ https://www.ncbi.nlm.nih.gov/pubmed/33846307 http://dx.doi.org/10.1038/s41419-021-03676-x |
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