SUMOylation Represses Nanog Expression via Modulating Transcription Factors Oct4 and Sox2

被引:40
作者
Wu, Yongyan [1 ]
Guo, Zekun
Wu, Haibo
Wang, Xiaohai
Yang, Lixia
Shi, Xiaoyan
Du, Juan
Tang, Bo
Li, Wenzhong
Yang, Liping
Zhang, Yong [1 ]
机构
[1] NW A&F Univ, Coll Vet Med, Key Lab Anim Biotechnol, Minist Agr, Yangling, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
EMBRYONIC STEM-CELLS; SUBCELLULAR-LOCALIZATION; PROTEIN SUMOYLATION; MOUSE EMBRYOS; DNA-BINDING; SUMO; PLURIPOTENCY; STABILITY; UBIQUITIN; LINEAGES;
D O I
10.1371/journal.pone.0039606
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nanog is a pivotal transcription factor in embryonic stem (ES) cells and is essential for maintaining the pluripotency and self-renewal of ES cells. SUMOylation has been proved to regulate several stem cell markers' function, such as Oct4 and Sox2. Nanog is strictly regulated by Oct4/Sox2 heterodimer. However, the direct effects of SUMOylation on Nanog expression remain unclear. In this study, we reported that SUMOylation repressed Nanog expression. Depletion of Sumo1 or its conjugating enzyme Ubc9 increased the expression of Nanog, while high SUMOylation reduced its expression. Interestingly, we found that SUMOylation of Oct4 and Sox2 regulated Nanog in an opposing manner. SUMOylation of Oct4 enhanced Nanog expression, while SUMOylated Sox2 inhibited its expression. Moreover, SUMOylation of Oct4 by Pias2 or Sox2 by Pias3 impaired the interaction between Oct4 and Sox2. Taken together, these results indicate that SUMOylation has a negative effect on Nanog expression and provides new insights into the mechanism of SUMO modification involved in ES cells regulation.
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页数:12
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