SUMOylation of Tr2 orphan receptor involves Pml and fine-tunes Oct4 expression in stem cells

Sung Wook Park, Xinli Hu, Pawan Gupta, Ya Ping Lin, Sung Gil Ha, Li Na Wei*

*此作品的通信作者

研究成果: 期刊稿件文章同行評審

46 引文 斯高帕斯(Scopus)

摘要

The Tr2 orphan nuclear receptor can be SUMOylated, resulting in the replacement of coregulators recruited to the regulatory region of its endogenous target gene, Oct4. UnSUMOylated Tr2 activates Oct4, enhancing embryonal carcinoma-cell proliferation, and is localized to the promyelocytic leukemia (Pml) nuclear bodies. When its abundance is elevated, Tr2 is SUMOylated at Lys238 and seems to be released from the nuclear bodies to act as a repressor. SUMOylation of Tr2 induces an exchange of its coregulators: corepressor Rip140 replaces coactivator Pcaf, which switches Tr2 from an activator to a repressor. This involves dynamic partitioning of Tr2 into Pml-containing and Pml-free pools. These results support a model where SUMOylation-dependent partitioning and differential coregulator recruitment contribute to the maintenance of a homeostatic supply of activating, as opposed to repressive, Tr2, thus fine-tuning Oct4 expression and regulating stem-cell proliferation.

原文英語
頁(從 - 到)68-75
頁數8
期刊Nature Structural and Molecular Biology
14
發行號1
DOIs
出版狀態已出版 - 01 2007
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