The chromatin accessibility landscape reveals distinct transcriptional regulation in the induction of human primordial germ cell-like cells from pluripotent stem cells
Xiaoman Wang, Veeramohan Veerapandian, Xinyan Yang, Ke Song, Xiaoheng Xu, Manman Cui, Weiyan Yuan, Yaping Huang, Xinyu Xia, Zhaokai Yao, Cong Wan, Fang Luo, Xiuling Song, Xiaoru Wang, Yi Zheng, Andrew P. Hutchins, Ralf Jauch, Meiyan Liang, Chenhong Wang, Zhaoting Liu, Gang Chang, Xiaoyang Zhao
Abstract
In vitro induction of human primordial germ cell-like cells (hPGCLCs) provides an ideal platform to recapitulate hPGC development. However, the detailed molecular mechanisms regulating the induction of hPGCLCs remain largely uncharacterized. Here, we profiled the chromatin accessibility and transcriptome dynamics throughout the process of hPGCLC induction. Genetic ablation of SOX15 indicated the crucial roles of SOX15 in the maintenance of hPGCLCs. Mechanistically, SOX15 exerted its roles via suppressing somatic gene expression and sustaining latent pluripotency. Notably, ETV5, a downstream regulator of SOX15, was also uncovered to be essential for hPGCLC maintenance. Finally, a stepwise switch of OCT4/SOX2, OCT4/SOX17, and OCT4/SOX15 binding motifs were found to be enriched in closed-to-open regions of human embryonic stem cells, and early- and late-stage hPGCLCs, respectively. Collectively, our data characterized the chromatin accessibility and transcriptome landscapes throughout hPGCLC induction and defined the SOX15-mediated regulatory networks underlying this process.