Single-cell RNA sequencing reveals the landscape of early female germ cell development

• Published in: The FASEB journal Vol. 34; no. 9; p. 12634
• Main Authors: Zhao, Zheng-Hui, Ma, Jun-Yu, Meng, Tie-Gang, Wang, Zhen-Bo, Yue, Wei, Zhou, Qian, Li, Sen, Feng, Xie, Hou, Yi, Schatten, Heide, Ou, Xiang-Hong, Sun, Qing-Yuan
• Format: Journal Article
• Language: English
• Published: United States 01.09.2020
• Subjects: Animals; Cell Differentiation; Female; Gene Expression Regulation, Developmental; Meiosis; Mice; Mice, Inbred C57BL; Mitosis; Oogenesis; Oogonia - cytology; Ovary - cytology; Sequence Analysis, RNA; Single-Cell Analysis; Transcriptome; scRNA-seq; developmental trajectory; oocyte; meiosis initiation
• DOI: 10.1096/fj.202001034RR

Meiosis initiation is a crucial step for the production of haploid gametes, which occurs from anterior to posterior in fetal ovaries. The asynchrony of the transition from mitosis to meiosis results in heterogeneity in the female germ cell populations, which limits the studies of meiosis initiation and progression at a higher resolution level. To dissect the process of meiosis initiation, we investigated the transcriptional profiles of 19 363 single germ cells collected from E12.5, E14.5, and E16.5 mouse fetal ovaries. Clustering analysis identified seven groups and defined dozens of corresponding transcription factors, providing a global view of cellular differentiation from primordial germ cells toward meiocytes. Furthermore, we explored the dynamics of gene expression within the developmental trajectory with special focus on the critical state of meiosis. We found that meiosis initiation occurs as early as E12.5 and the cluster of oogonia_4 is the critical state between mitosis and meiosis. Our data provide key insights into the transcriptome features of peri-meiotic female germ cells, which offers new information not only on meiosis initiation and progression but also on screening pathogenic mutations in meiosis-associated diseases.