Loss of Tet hydroxymethylase activity causes mouse embryonic stem cell differentiation bias and developmental defects

• Published in: Science China. Life sciences 2024-10, Vol.67 (10), p.2132-2148
• Main Authors: Wang, Mengting, Wang, Liping, Huang, Yanxin, Qiao, Zhibin, Yi, Shanru, Zhang, Weina, Wang, Jing, Yang, Guang, Cui, Xinyu, Kou, Xiaochen, Zhao, Yanhong, Wang, Hong, Jiang, Cizhong, Gao, Shaorong, Chen, Jiayu
• Format: Article
• Language: English
• Subjects: Biomedical and Life Sciences; Cell differentiation; Demethylation; DNA methylation; Embryo cells; Embryogenesis; Gene expression; Growth rate; Infertility; Lethality; Life Sciences; Pluripotency; Regulatory sequences; Research Paper; Stem cells
• ISSN: 1674-7305; 1869-1889; 1869-1889
• DOI: 10.1007/s11427-024-2631-x

The TET family is well known for active DNA demethylation and plays important roles in regulating transcription, the epigenome and development. Nevertheless, previous studies using knockdown (KD) or knockout (KO) models to investigate the function of TET have faced challenges in distinguishing its enzymatic and nonenzymatic roles, as well as compensatory effects among TET family members, which has made the understanding of the enzymatic role of TET not accurate enough. To solve this problem, we successfully generated mice catalytically inactive for specific Tet members ( Tet m/m ). We observed that, compared with the reported KO mice, mutant mice exhibited distinct developmental defects, including growth retardation, sex imbalance, infertility, and perinatal lethality. Notably, Tet m/m mouse embryonic stem cells (mESCs) were successfully established but entered an impaired developmental program, demonstrating extended pluripotency and defects in ectodermal differentiation caused by abnormal DNA methylation. Intriguingly, Tet3 , traditionally considered less critical for mESCs due to its lower expression level, had a significant impact on the global hydroxymethylation, gene expression, and differentiation potential of mESCs. Notably, there were common regulatory regions between Tet1 and Tet3 in pluripotency regulation. In summary, our study provides a more accurate reference for the functional mechanism of Tet hydroxymethylase activity in mouse development and ESC pluripotency regulation.