2011 Collaborative Innovation Center of Tianjin for Medical Epigenetics, Department of Biochemistry and Molecular Biology, Tianjin Key Laboratory of Medical Epigenetics, Tianjin Medical University, Tianjin, China.
Oncogene. 2013 Aug 8;32(32):3711-21. doi: 10.1038/onc.2012.386. Epub 2012 Aug 27.
The p53 tumor suppressor is important in many aspects of cell biology. Tight regulation of p53 is thus imperative for maintaining cell homeostasis and preventing tumorigenesis. The stabilization and activity of p53 is primarily regulated by MDM2, which is encoded for by HDM2. However, how the expression and activity of MDM2 is regulated remains largely unknown. Here, we report a novel BTB and BEN domains-containing protein, RBB. We demonstrated that RBB is a novel transcriptional repressor binding specific DNA motif via a homodimer and interacting with the nucleosome remodeling and deacetylase (NuRD) complex. Genome wide transcription target analysis by ChIP sequencing revealed that RBB represses the transcription of a series of functionally important genes including HDM2. We showed that RBB recruits the NuRD complex to the internal promoter of HDM2 and inhibits the expression of MDM2 protein, leading to subsequent stabilization of tumor suppressor p53. Significantly, we showed that RBB suppresses cell proliferation and sensitizes cells to DNA damage-induced apoptosis. Our data indicate that RBB is a novel transcriptional repressor and an important regulator of p53 pathway.
p53 肿瘤抑制因子在细胞生物学的许多方面都很重要。因此,严格调控 p53 对于维持细胞内稳态和预防肿瘤发生至关重要。p53 的稳定和活性主要受 MDM2 调节,而 MDM2 则由 HDM2 编码。然而,MDM2 的表达和活性如何受到调节在很大程度上仍是未知的。在这里,我们报告了一种新型的 BTB 和 BEN 结构域蛋白 RBB。我们证明 RBB 是一种新型的转录抑制因子,通过同源二聚体结合特异性 DNA 基序,并与核小体重塑和去乙酰化酶(NuRD)复合物相互作用。通过 ChIP-seq 进行的全基因组转录靶标分析表明,RBB 抑制一系列功能重要基因的转录,包括 HDM2。我们表明 RBB 将 NuRD 复合物募集到 HDM2 的内部启动子,抑制 MDM2 蛋白的表达,从而导致肿瘤抑制因子 p53 的后续稳定。重要的是,我们表明 RBB 抑制细胞增殖并使细胞对 DNA 损伤诱导的细胞凋亡敏感。我们的数据表明,RBB 是一种新型的转录抑制因子,是 p53 通路的重要调节因子。