Phosphorylated p68 RNA helicase activates snail1 transcription by promoting HDAC1 dissociation from the snail1 promoter

被引:33
作者
Carter, C. L. [1 ]
Lin, C. [1 ]
Liu, C-Y [1 ]
Yang, L. [1 ]
Liu, Z-R [1 ]
机构
[1] Georgia State Univ, Dept Biol, Atlanta, GA 30303 USA
关键词
p68 RNA helicase; Snail1; transcription activation; HDAC1; Mi-2/NuRD; EPITHELIAL-MESENCHYMAL TRANSITION; ESTROGEN-RECEPTOR-ALPHA; E-CADHERIN EXPRESSION; HISTONE ACETYLATION; TUMOR PROGRESSION; BETA-CATENIN; CHROMATIN; PROTEIN; COMPLEX; CANCER;
D O I
10.1038/onc.2010.276
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 nuclear p68 RNA helicase is a prototypical member of the DEAD-box family of RNA helicases. p68 RNA helicase has been implicated in cell proliferation and early organ development and maturation. However, the functional role of p68 RNA helicase in these biological processes at the molecular level is not well understood. We previously reported that tyrosine phosphorylation of p68 RNA helicase mediates the effects of platelet-derived growth factor (PDGF) in induction of epithelial mesenchymal transition by promoting beta-catenin nuclear translocation. Here, we report that phosphorylation of p68 RNA helicase at Y593 upregulates transcription of the Snail1 gene. The phosphorylated p68 activates transcription of the Snail1 gene by promoting histone deacetylase (HDAC) 1 dissociation from the Snail1 promoter. Our results showed that p68 interacted with the nuclear remodeling and deacetylation complex MBD3:Mi-2/NuRD. Thus, our data suggested that a DEAD-box RNA unwindase could potentially regulate gene expression by functioning as a protein 'displacer' to modulate protein-protein interactions at the chromatin-remodeling complex. Oncogene (2010) 29, 5427-5436; doi: 10.1038/onc.2010.276; published online 2 August 2010
引用
收藏
页码:5427 / 5436
页数:10
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