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Smek promotes histone deacetylation to suppress transcription of Wnt target gene brachyury in pluripotent embryonic stem cells

摘要In embryonic stem cells (ESCs),Wnt-responsive development-related genes are silenced to maintain pluripotency and their expression is activated during differentiation. Acetylation of histones by histone acetyitransferases stimulates transcription,whereas deacetylation of histones by HDACs is correlated with transcriptional repression.Although Wnt-mediated gene transcription has been intimately linked to the acetylation or deacetylation of histones,how Wnt signaling regulates this type of histone modification is poorly understood. Here,we report that Smek,a regulatory subunit of protein phosphatase 4 (PP4) complex,plays an important role in histone deacetylation and silencing of the Wnt-responsive gene,brachyury,in ESCs. Smek mediates recruitment of PP4c and HDAC1 to the Tcf/Lef binding site of the brachyury promoter and inhibits brachyury expression in ESCs. Activation of Wnt signaling during differentiation causes disruption of the Smek/PP4c/HDAC1 complex,resulting in an increase in histones H3 and H4 acetylation at the brachyury gene locus. These results suggest that the Smek-containing PP4 complex represses transcription of Wnt-responsive development-related genes through histone deacetylation,and that this complex is essential for ESC pluripotency maintenance.

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DOI 10.1038/cr.2011.47
发布时间 2011-09-08(万方平台首次上网日期,不代表论文的发表时间)
基金项目
the CIRM Basic Biology Award((RB1-01353-1)) NIH((1R01NS067213-01A1))
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细胞研究(英文版)

细胞研究(英文版)

2011年21卷6期

911-921页

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