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YY1参与破骨细胞分化过程中RANKL诱导的抗酒石酸酸性磷酸酶基因的转录。

YY1 is involved in RANKL-induced transcription of the tartrate-resistant acid phosphatase gene in osteoclast differentiation.

作者信息

Shi Zhenqi, Silveira Alexandra, Patel Payal, Feng Xu

机构信息

Department of Pathology, University of Alabama at Birmingham, 1670 University BLVD, VH G046B, Birmingham, AL 35294, USA.

出版信息

Gene. 2004 Dec 8;343(1):117-26. doi: 10.1016/j.gene.2004.08.009.

Abstract

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.

摘要

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。

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