Cargando…
Single-cell RNA sequencing reveals regulation of fetal ovary development in the monkey (Macaca fascicularis)
Germ cells are vital for reproduction and heredity. However, the mechanisms underlying female germ cell development in primates, especially in late embryonic stages, remain elusive. Here, we performed single-cell RNA sequencing of 12,471 cells from whole fetal ovaries, and explored the communication...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Singapore
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7769980/ https://www.ncbi.nlm.nih.gov/pubmed/33372178 http://dx.doi.org/10.1038/s41421-020-00219-0 |
_version_ | 1783629432159731712 |
---|---|
author | Zhao, Zheng-Hui Li, Chun-Yang Meng, Tie-Gang Wang, Yan Liu, Wen-Bo Li, Ang Cai, Yi-Jun Hou, Yi Schatten, Heide Wang, Zhen-Bo Sun, Qing-Yuan Sun, Qiang |
author_facet | Zhao, Zheng-Hui Li, Chun-Yang Meng, Tie-Gang Wang, Yan Liu, Wen-Bo Li, Ang Cai, Yi-Jun Hou, Yi Schatten, Heide Wang, Zhen-Bo Sun, Qing-Yuan Sun, Qiang |
author_sort | Zhao, Zheng-Hui |
collection | PubMed |
description | Germ cells are vital for reproduction and heredity. However, the mechanisms underlying female germ cell development in primates, especially in late embryonic stages, remain elusive. Here, we performed single-cell RNA sequencing of 12,471 cells from whole fetal ovaries, and explored the communications between germ cells and niche cells. We depicted the two waves of oogenesis at single-cell resolution and demonstrated that progenitor theca cells exhibit similar characteristics to Leydig cells in fetal monkey ovaries. Notably, we found that ZGLP1 displays differentially expressed patterns between mouse and monkey, which is not overlapped with NANOG in monkey germ cells, suggesting its role in meiosis entry but not in activating oogenic program in primates. Furthermore, the majority of germ cell clusters that sharply express PRDM9 and SPO11 might undergo apoptosis after cyst breakdown, leading to germ cell attrition. Overall, our work provides new insights into the molecular and cellular basis of primate fetal ovary development at single-cell resolution. |
format | Online Article Text |
id | pubmed-7769980 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-77699802021-01-07 Single-cell RNA sequencing reveals regulation of fetal ovary development in the monkey (Macaca fascicularis) Zhao, Zheng-Hui Li, Chun-Yang Meng, Tie-Gang Wang, Yan Liu, Wen-Bo Li, Ang Cai, Yi-Jun Hou, Yi Schatten, Heide Wang, Zhen-Bo Sun, Qing-Yuan Sun, Qiang Cell Discov Article Germ cells are vital for reproduction and heredity. However, the mechanisms underlying female germ cell development in primates, especially in late embryonic stages, remain elusive. Here, we performed single-cell RNA sequencing of 12,471 cells from whole fetal ovaries, and explored the communications between germ cells and niche cells. We depicted the two waves of oogenesis at single-cell resolution and demonstrated that progenitor theca cells exhibit similar characteristics to Leydig cells in fetal monkey ovaries. Notably, we found that ZGLP1 displays differentially expressed patterns between mouse and monkey, which is not overlapped with NANOG in monkey germ cells, suggesting its role in meiosis entry but not in activating oogenic program in primates. Furthermore, the majority of germ cell clusters that sharply express PRDM9 and SPO11 might undergo apoptosis after cyst breakdown, leading to germ cell attrition. Overall, our work provides new insights into the molecular and cellular basis of primate fetal ovary development at single-cell resolution. Springer Singapore 2020-12-29 /pmc/articles/PMC7769980/ /pubmed/33372178 http://dx.doi.org/10.1038/s41421-020-00219-0 Text en © The Author(s) 2020 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 Zhao, Zheng-Hui Li, Chun-Yang Meng, Tie-Gang Wang, Yan Liu, Wen-Bo Li, Ang Cai, Yi-Jun Hou, Yi Schatten, Heide Wang, Zhen-Bo Sun, Qing-Yuan Sun, Qiang Single-cell RNA sequencing reveals regulation of fetal ovary development in the monkey (Macaca fascicularis) |
title | Single-cell RNA sequencing reveals regulation of fetal ovary development in the monkey (Macaca fascicularis) |
title_full | Single-cell RNA sequencing reveals regulation of fetal ovary development in the monkey (Macaca fascicularis) |
title_fullStr | Single-cell RNA sequencing reveals regulation of fetal ovary development in the monkey (Macaca fascicularis) |
title_full_unstemmed | Single-cell RNA sequencing reveals regulation of fetal ovary development in the monkey (Macaca fascicularis) |
title_short | Single-cell RNA sequencing reveals regulation of fetal ovary development in the monkey (Macaca fascicularis) |
title_sort | single-cell rna sequencing reveals regulation of fetal ovary development in the monkey (macaca fascicularis) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7769980/ https://www.ncbi.nlm.nih.gov/pubmed/33372178 http://dx.doi.org/10.1038/s41421-020-00219-0 |
work_keys_str_mv | AT zhaozhenghui singlecellrnasequencingrevealsregulationoffetalovarydevelopmentinthemonkeymacacafascicularis AT lichunyang singlecellrnasequencingrevealsregulationoffetalovarydevelopmentinthemonkeymacacafascicularis AT mengtiegang singlecellrnasequencingrevealsregulationoffetalovarydevelopmentinthemonkeymacacafascicularis AT wangyan singlecellrnasequencingrevealsregulationoffetalovarydevelopmentinthemonkeymacacafascicularis AT liuwenbo singlecellrnasequencingrevealsregulationoffetalovarydevelopmentinthemonkeymacacafascicularis AT liang singlecellrnasequencingrevealsregulationoffetalovarydevelopmentinthemonkeymacacafascicularis AT caiyijun singlecellrnasequencingrevealsregulationoffetalovarydevelopmentinthemonkeymacacafascicularis AT houyi singlecellrnasequencingrevealsregulationoffetalovarydevelopmentinthemonkeymacacafascicularis AT schattenheide singlecellrnasequencingrevealsregulationoffetalovarydevelopmentinthemonkeymacacafascicularis AT wangzhenbo singlecellrnasequencingrevealsregulationoffetalovarydevelopmentinthemonkeymacacafascicularis AT sunqingyuan singlecellrnasequencingrevealsregulationoffetalovarydevelopmentinthemonkeymacacafascicularis AT sunqiang singlecellrnasequencingrevealsregulationoffetalovarydevelopmentinthemonkeymacacafascicularis |