Department of Developmental and Surgical Science, University of Minnesota School of Dentistry, 515 Delaware St SE, Minneapolis, Minnesota 55455, USA.
J Cell Biochem. 2010 Apr 1;109(5):967-74. doi: 10.1002/jcb.22475.
The microphthalmia-associated transcription factor (Mitf) regulates gene expression required for osteoclast differentiation. Genes regulated by Mitf have been previously identified. However, proteins that interact and regulate Mitf's activity in osteoclasts are not well known. Here, we report that POH1, a subunit of the 19S proteasome lid is a regulator of Mitf. We show that POH1 and Mitf interact in osteoclasts and that this interaction is dependent on RANKL signaling. Overexpression of POH1 increased Mitf's activation of 5XGal4-TK and Acp5 promoters. The amino terminus of POH1 mediates the binding to Mitf and is sufficient to increase Mitf's transcriptional activity. Finally, we show that mutations in the JAMM motif of POH1 reduced Mitf activation of promoters. In summary, our results identify a novel mechanism of Mitf regulation in osteoclasts by POH1.
小眼畸形相关转录因子(Mitf)调节破骨细胞分化所需的基因表达。Mitf 调节的基因以前已经被鉴定过。然而,与破骨细胞中 Mitf 的活性相互作用并调节其活性的蛋白质尚不清楚。在这里,我们报告说,POH1 是 19S 蛋白酶体盖的一个亚基,是 Mitf 的调节剂。我们表明 POH1 和 Mitf 在破骨细胞中相互作用,这种相互作用依赖于 RANKL 信号。POH1 的过表达增加了 Mitf 对 5XGal4-TK 和 Acp5 启动子的激活。POH1 的氨基末端介导与 Mitf 的结合,足以增加 Mitf 的转录活性。最后,我们表明 POH1 的 JAMM 基序突变降低了 Mitf 对启动子的激活。总之,我们的结果确定了 POH1 通过破骨细胞中 Mitf 调节的新机制。