IκBζ expression is regulated by miR-124a

被引:32
作者
Lindenblatt, Charlotte [2 ]
Schulze-Osthoff, Klaus [1 ,2 ]
Totzke, Gudrun [2 ]
机构
[1] Univ Tubingen, Interfac Inst Biochem, D-72076 Tubingen, Germany
[2] Univ Dusseldorf, Inst Mol Med, Dusseldorf, Germany
关键词
I kappa B zeta; NF kappa B; microRNA-124a; gene expression; inflammation; apoptosis; ONCOPROTEIN BCL-3; MICRORNAS; CANCER; TRANSACTIVATION; DIFFERENTIATION; ASSOCIATION;
D O I
10.4161/cc.8.13.8816
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
I kappa B zeta belongs to the nuclear members of the I kappa B protein family. Its function in regulating the activity of the transcription factor NF kappa B is poorly understood. Here, we demonstrate that human I kappa B zeta is posttranscriptionally regulated by microRNA (miR)-124a. In HepG2 cells miR-124a was not endogenously expressed, but upon enforced expression dramatically inhibited the interleukin-1 beta-induced protein expression of I kappa B zeta. The predicted binding site for miR-124a in the 3'UTR of the I kappa B zeta mRNA revealed an imperfect match resulting in miR-124a-mediated suppression of I kappa B zeta expression through translational repression. Reporter gene analyses revealed that miR-124a targets I kappa B zeta mRNA through base pairing to the partially complementary sequence in the 3'UTR that was predicted as a binding site by in silico analysis. Furthermore, we demonstrate that the 7mer seed match is sufficient for recognition of the I kappa B zeta mRNA. Together, our data identify I kappa B zeta as a target of miR-124a that might be involved in the fine-tuning of NF kappa B-mediated gene expression.
引用
收藏
页码:2019 / 2023
页数:5
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