A repressive role of enhancer of zeste homolog 2 in 11β-hydroxysteroid dehydrogenase type 2 expression in the human placenta

被引:11
|
作者
Zuo, Rujuan [1 ,2 ]
Liu, Xiaohui [3 ]
Wang, Wangsheng [1 ,2 ]
Li, Wenjiao [1 ,2 ]
Ying, Hao [3 ]
Sun, Kang [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Ren Ji Hosp, Ctr Reprod Med, Shanghai 200135, Peoples R China
[2] Shanghai Key Lab Assisted Reprod & Reprod Genet, Shanghai 200135, Peoples R China
[3] Tongji Univ, Sch Med, Shanghai Matern & Infant Hosp 1, Shanghai 200135, Peoples R China
基金
中国国家自然科学基金;
关键词
E2F transcription factor; glucocorticoid; histone methylation; histone modification; placenta; trophoblast; 11-hydroxysteroid dehydrogenase 2; EZH2; fetal development; 11-BETA-HSD2; EXPRESSION; EPIGENETIC REGULATION; TRANSCRIPTION FACTOR; CELL-PROLIFERATION; METHYLATION; TROPHOBLAST; INHIBITION; EZH2; GLUCOCORTICOIDS; ACETYLATION;
D O I
10.1074/jbc.M116.765800
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The expression of 11-hydroxysteroid dehydrogenase type 2 (11-HSD2), which acts as a placental glucocorticoid barrier, is silenced in cytotrophoblasts but substantially up-regulated during syncytialization. However, the repressive mechanism of 11-HSD2 expression before syncytialization and how this repression is lifted during syncytialization remain mostly unresolved. Here we found that enhancer of zeste homolog 2 (EZH2) accounts for the silence of 11-HSD2 expression via trimethylation of histone H3 lysine 27 at the promoter of the 11-HSD2 gene. Further studies revealed that, upon syncytialization, human chorionic gonadotropin reduced the phosphorylation of retinoblastoma protein (pRB) via activation of the cAMP/PKA pathway, which sequesters E2F transcription factor 1 (E2F1), the transcription factor for EZH2 expression. As a result of inactivation of the pRB-E2F1-EZH2 pathway, the repressive marker trimethylation of histone H3 lysine 27 at the 11-HSD2 promoter is removed, which leads to the robust expression of 11-HSD2 during syncytialization.
引用
收藏
页码:7578 / 7587
页数:10
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