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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...

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Autores principales: Wang, Xin, Lai, Fengling, Shang, Dantong, Cheng, Yibin, Lan, Tian, Cheng, Hanhua, Zhou, Rongjia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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.
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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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