Ji Guanxu, Xiao Xiaoxiao, Huang Min, Wu Qiang
The State Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Macau, China.
Heliyon. 2022 Mar 15;8(3):e09105. doi: 10.1016/j.heliyon.2022.e09105. eCollection 2022 Mar.
Jmjd6 is a conserved nuclear protein which possesses histone arginine demethylation and lysyl hydroxylase activity. Previous studies have revealed that Jmjd6 is essential for cell differentiation and embryo development. However, the role of Jmjd6 in mammalian ES cell identity and reprogramming has been unclear. Here we report that depletion of Jmjd6 not only results in downregulation of pluripotency genes but also is implicated in apoptosis, glycolysis, cell cycle and protein hydroxylation. We also revealed the reduction of BrdU incorporation in depleted cells. Reprogramming efficiency of MEFs can be enhanced with Jmjd6 overexpression while the efficiency was reduced upon depletion. Together, these results suggest that Jmjd6 can regulate ES cell homeostasis and enhance somatic cell reprogramming.
Jmjd6是一种保守的核蛋白,具有组蛋白精氨酸去甲基化和赖氨酸羟化酶活性。先前的研究表明,Jmjd6对细胞分化和胚胎发育至关重要。然而,Jmjd6在哺乳动物胚胎干细胞特性和重编程中的作用尚不清楚。在此我们报告,Jmjd6的缺失不仅导致多能性基因的下调,还与细胞凋亡、糖酵解、细胞周期和蛋白质羟基化有关。我们还发现,在缺失Jmjd6的细胞中,BrdU掺入减少。Jmjd6过表达可提高成纤维细胞的重编程效率,而缺失Jmjd6则会降低重编程效率。总之,这些结果表明,Jmjd6可以调节胚胎干细胞的稳态并增强体细胞重编程。