Shi Zhenqi, Silveira Alexandra, Patel Payal, Feng Xu
Department of Pathology, University of Alabama at Birmingham, 1670 University BLVD, VH G046B, Birmingham, AL 35294, USA.
Gene. 2004 Dec 8;343(1):117-26. doi: 10.1016/j.gene.2004.08.009.
Receptor activator of nuclear factor kappa B (NF-kappaB) ligand (RANKL), a critical activator of osteoclast differentiation, plays a pivotal role in tartrate-resistant acid phosphatase (TRAP) gene expression. Previously, we showed that upstream stimulatory factors (USF) 1 and 2 are implicated in the RANKL-induced TRAP transcriptional activation via a 12-bp USF binding site in the TRAP promoter. In that study, we also demonstrated that a RANKL-induced nuclear protein binds to a 50-bp oligonucleotide (Oligo IV) corresponding to a distinct TRAP promoter region. Here we report the identification and functional characterization of the nuclear protein binding to Oligo IV. We identified a 21-bp sequence CTGTTTATGATGGCGAGGGGG in Oligo IV that specifically binds the RANKL-induced nuclear protein from RAW264.7 cells by performing a series of competition assays. Computer analysis of the 21-bp sequence revealed that the sequence contains a putative Yin Yang 1 (YY1) binding site overlapped with a putative activator protein-2 (AP-2) binding site. Competition and supershift assays indicated that the nuclear protein binding to the 21-bp sequence is YY1, not AP-2. Functionally, mutation of the YY1-binding site resulted in a reduction in the RANKL-induced TRAP transcription in RAW264.7 cells, demonstrating that YY1 positively regulates RANKL-induced TRAP transcriptional activation. In conclusion, our data demonstrated that YY1 plays a functional role in RANKL-mediated TRAP gene expression during osteoclast differentiation.
核因子κB(NF-κB)受体激活剂配体(RANKL)是破骨细胞分化的关键激活剂,在抗酒石酸酸性磷酸酶(TRAP)基因表达中起关键作用。此前,我们发现上游刺激因子(USF)1和2通过TRAP启动子中的一个12碱基对的USF结合位点参与RANKL诱导的TRAP转录激活。在该研究中,我们还证明RANKL诱导的一种核蛋白与对应于TRAP启动子一个不同区域的50碱基对寡核苷酸(寡核苷酸IV)结合。在此,我们报告了与寡核苷酸IV结合的核蛋白的鉴定及其功能特性。通过一系列竞争试验,我们在寡核苷酸IV中鉴定出一个21碱基对的序列CTGTTTATGATGGCGAGGGGG,它特异性结合RAW264.7细胞中RANKL诱导的核蛋白。对该21碱基对序列的计算机分析显示,该序列包含一个推定的阴阳1(YY1)结合位点,与一个推定的激活蛋白2(AP-2)结合位点重叠。竞争试验和超迁移试验表明,与21碱基对序列结合的核蛋白是YY1,而非AP-2。在功能上,YY1结合位点的突变导致RAW264.7细胞中RANKL诱导的TRAP转录减少,表明YY1正向调节RANKL诱导的TRAP转录激活。总之,我们的数据表明YY1在破骨细胞分化过程中RANKL介导的TRAP基因表达中发挥功能作用。