Frontiers in Cell and Developmental Biology (Sep 2021)
The Dynamic Changes of Transcription Factors During the Development Processes of Human Biparental and Uniparental Embryos
- Chenxi Zhang,
- Chenxi Zhang,
- Chenxi Zhang,
- Conghui Li,
- Conghui Li,
- Conghui Li,
- Conghui Li,
- Conghui Li,
- Ling Yang,
- Ling Yang,
- Ling Yang,
- Ling Yang,
- Lizhi Leng,
- Lizhi Leng,
- Lizhi Leng,
- Dragomirka Jovic,
- Dragomirka Jovic,
- Jun Wang,
- Jun Wang,
- Jun Wang,
- Fang Fang,
- Fang Fang,
- Guibo Li,
- Guibo Li,
- Depeng Zhao,
- Xuemei Li,
- Lin Lin,
- Yonglun Luo,
- Yonglun Luo,
- Yonglun Luo,
- Yonglun Luo,
- Yonglun Luo,
- Yonglun Luo,
- Yonglun Luo,
- Lars Bolund,
- Lars Bolund,
- Lars Bolund,
- Lars Bolund,
- Jinrong Huang,
- Jinrong Huang,
- Jinrong Huang,
- Jinrong Huang,
- Jinrong Huang,
- Ge Lin,
- Ge Lin,
- Ge Lin,
- Fengping Xu,
- Fengping Xu,
- Fengping Xu,
- Fengping Xu,
- Fengping Xu,
- Fengping Xu
Affiliations
- Chenxi Zhang
- College of Life Sciences, University of Chinese Academy of Sciences, Beijing, China
- Chenxi Zhang
- BGI-Shenzhen, Shenzhen, China
- Chenxi Zhang
- Lars Bolund Institute of Regenerative Medicine, BGI-Qingdao, BGI-Shenzhen, Qingdao, China
- Conghui Li
- College of Life Sciences, University of Chinese Academy of Sciences, Beijing, China
- Conghui Li
- BGI-Shenzhen, Shenzhen, China
- Conghui Li
- Lars Bolund Institute of Regenerative Medicine, BGI-Qingdao, BGI-Shenzhen, Qingdao, China
- Conghui Li
- Qingdao-Europe Advanced Institute for Life Sciences, BGI-Shenzhen, Qingdao, China
- Conghui Li
- China National GeneBank, BGI-Shenzhen, Shenzhen, China
- Ling Yang
- BGI-Shenzhen, Shenzhen, China
- Ling Yang
- Lars Bolund Institute of Regenerative Medicine, BGI-Qingdao, BGI-Shenzhen, Qingdao, China
- Ling Yang
- Qingdao-Europe Advanced Institute for Life Sciences, BGI-Shenzhen, Qingdao, China
- Ling Yang
- China National GeneBank, BGI-Shenzhen, Shenzhen, China
- Lizhi Leng
- School of Basic Medical Science, Institute of Reproductive and Stem Cell Engineering, Central South University, Changsha, China
- Lizhi Leng
- Key Laboratory of Reproductive and Stem Cells Engineering, Ministry of Health, Changsha, China
- Lizhi Leng
- Reproductive and Genetic Hospital of CITIC-Xiangya, Changsha, China
- Dragomirka Jovic
- BGI-Shenzhen, Shenzhen, China
- Dragomirka Jovic
- Qingdao-Europe Advanced Institute for Life Sciences, BGI-Shenzhen, Qingdao, China
- Jun Wang
- College of Life Sciences, University of Chinese Academy of Sciences, Beijing, China
- Jun Wang
- BGI-Shenzhen, Shenzhen, China
- Jun Wang
- Lars Bolund Institute of Regenerative Medicine, BGI-Qingdao, BGI-Shenzhen, Qingdao, China
- Fang Fang
- Lars Bolund Institute of Regenerative Medicine, BGI-Qingdao, BGI-Shenzhen, Qingdao, China
- Fang Fang
- China National GeneBank, BGI-Shenzhen, Shenzhen, China
- Guibo Li
- BGI-Shenzhen, Shenzhen, China
- Guibo Li
- China National GeneBank, BGI-Shenzhen, Shenzhen, China
- Depeng Zhao
- Department of Reproductive Medicine, Affiliated Shenzhen Maternity and Child Healthcare Hospital, Southern Medical University, Shenzhen, China
- Xuemei Li
- Department of Reproductive Medicine, Affiliated Shenzhen Maternity and Child Healthcare Hospital, Southern Medical University, Shenzhen, China
- Lin Lin
- 0Department of Biomedicine, Aarhus University, Aarhus, Denmark
- Yonglun Luo
- College of Life Sciences, University of Chinese Academy of Sciences, Beijing, China
- Yonglun Luo
- BGI-Shenzhen, Shenzhen, China
- Yonglun Luo
- Lars Bolund Institute of Regenerative Medicine, BGI-Qingdao, BGI-Shenzhen, Qingdao, China
- Yonglun Luo
- Qingdao-Europe Advanced Institute for Life Sciences, BGI-Shenzhen, Qingdao, China
- Yonglun Luo
- China National GeneBank, BGI-Shenzhen, Shenzhen, China
- Yonglun Luo
- 0Department of Biomedicine, Aarhus University, Aarhus, Denmark
- Yonglun Luo
- 1Steno Diabetes Center Aarhus, Aarhus University Hospital, Aarhus, Denmark
- Lars Bolund
- BGI-Shenzhen, Shenzhen, China
- Lars Bolund
- Lars Bolund Institute of Regenerative Medicine, BGI-Qingdao, BGI-Shenzhen, Qingdao, China
- Lars Bolund
- Qingdao-Europe Advanced Institute for Life Sciences, BGI-Shenzhen, Qingdao, China
- Lars Bolund
- 0Department of Biomedicine, Aarhus University, Aarhus, Denmark
- Jinrong Huang
- BGI-Shenzhen, Shenzhen, China
- Jinrong Huang
- Lars Bolund Institute of Regenerative Medicine, BGI-Qingdao, BGI-Shenzhen, Qingdao, China
- Jinrong Huang
- Qingdao-Europe Advanced Institute for Life Sciences, BGI-Shenzhen, Qingdao, China
- Jinrong Huang
- China National GeneBank, BGI-Shenzhen, Shenzhen, China
- Jinrong Huang
- 2Department of Biology, University of Copenhagen, Copenhagen, Denmark
- Ge Lin
- School of Basic Medical Science, Institute of Reproductive and Stem Cell Engineering, Central South University, Changsha, China
- Ge Lin
- Key Laboratory of Reproductive and Stem Cells Engineering, Ministry of Health, Changsha, China
- Ge Lin
- Reproductive and Genetic Hospital of CITIC-Xiangya, Changsha, China
- Fengping Xu
- College of Life Sciences, University of Chinese Academy of Sciences, Beijing, China
- Fengping Xu
- BGI-Shenzhen, Shenzhen, China
- Fengping Xu
- Lars Bolund Institute of Regenerative Medicine, BGI-Qingdao, BGI-Shenzhen, Qingdao, China
- Fengping Xu
- Qingdao-Europe Advanced Institute for Life Sciences, BGI-Shenzhen, Qingdao, China
- Fengping Xu
- China National GeneBank, BGI-Shenzhen, Shenzhen, China
- Fengping Xu
- 3BGI Cell, BGI-Shenzhen, Shenzhen, China
- DOI
- https://doi.org/10.3389/fcell.2021.709498
- Journal volume & issue
-
Vol. 9
Abstract
Previous studies have revealed that transcription factors (TFs) play important roles in biparental (BI) early human embryogenesis. However, the contribution of TFs during early uniparental embryo development is still largely unknown. Here we systematically studied the expression profiles of transcription factors in early embryonic development and revealed the dynamic changes of TFs in human biparental and uniparental embryogenesis by single-cell RNA sequencing (scRNA-seq). In general, the TF expression model of uniparental embryos showed a high degree of conformity with biparental embryos. The detailed network analysis of three different types of embryos identified that 10 out of 17 hub TFs were shared or specifically owned, such as ZNF480, ZNF581, PHB, and POU5F1, were four shared TFs, ZFN534, GTF3A, ZNF771, TEAD4, and LIN28A, were androgenic (AG) specific TFs, and ZFP42 was the only one parthenogenetic (PG) specific TF. All the four shared TFs were validated using human embryonic stem cell (hESC) differentiation experiments; most of their target genes are responsible for stem cell maintenance and differentiation. We also found that Zf-C2H2, HMG, and MYB were three dominant transcription factor families that appeared in early embryogenesis. Altogether, our work provides a comprehensive regulatory framework and better understanding of TF function in human biparental and uniparental embryogenesis.
Keywords
- uniparental embryos
- single-cell RNA sequencing
- transcription factors
- gene expression
- embryo development