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

被引:39
作者
Zhao, Zheng-Hui [1 ,2 ]
Ma, Jun-Yu [3 ]
Meng, Tie-Gang [1 ,3 ]
Wang, Zhen-Bo [1 ,2 ]
Yue, Wei [1 ,2 ]
Zhou, Qian [1 ,2 ]
Li, Sen [3 ]
Feng, Xie [3 ]
Hou, Yi [1 ]
Schatten, Heide [4 ]
Ou, Xiang-Hong [3 ]
Sun, Qing-Yuan [1 ,3 ]
机构
[1] Chinese Acad Sci, Inst Zool, State Key Lab Stem Cell & Reprod Biol, Beijing, Peoples R China
[2] Univ Chinese Acad Sci, Coll Life Sci, Beijing, Peoples R China
[3] Guangdong Second Prov Gen Hosp, Fertil Preservat Lab, Reprod Med Ctr, Guangzhou, Peoples R China
[4] Univ Missouri, Dept Vet Pathobiol, Columbia, MO USA
基金
中国国家自然科学基金;
关键词
developmental trajectory; meiosis initiation; oocyte; scRNA-seq; PRIMORDIAL FOLLICLE; FATE SPECIFICATION; DNA METHYLATION; MOUSE; DIFFERENTIATION; TROPHECTODERM; SUBUNIT; GENES; TAF4B; CDX2;
D O I
10.1096/fj.202001034RR
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:12634 / 12645
页数:12
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