Zheng Lanlan, Liu Heng, Wang Pin, Song Weihong, Sun Xiulian
Qilu Hospital of Shandong University, 107 Wenhuaxi Rd., Jinan, Shandong Province, 250012, China.
Curr Alzheimer Res. 2014 Feb;11(2):156-64. doi: 10.2174/1567205010666131212114907.
Regulator of calcineurin 1 (RCAN1) has been implicated in pathogenesis of neurodegeneration and various cancers. Recently, we showed that RCAN1 expression was elevated in Down Syndrome and Alzheimer's disease and its expression transpose over induced neuronal apoptosis. As NF-κB is an important transcription factor involved in cell survival and RCAN1 played vital roles in cell viability, we examined whether NF-κB regulates RCAN1 gene expression. Our results here showed that the RCAN1 isoform 4 gene transcription can be activated by NF-κB signaling. NF-κB activated RCAN1 isoform 4 gene promoter. Luciferase assay, electrophoretic mobility shift assay (EMSA) and chromatin immunoprecipitation identified a NF-κB responsive element in the region of -576-554bp of the RCAN1 isoform 4 promoter. Activation of RCAN1 gene expression by NF-κB is independent from the calcineurin-NFAT signaling since the NF-κB responsive element was distinct from the NFAT binding sites that was previously identified in the region of -350-166bp. Indeed, activation of calcineurin-NFAT signaling decreased NF-κB transcriptional activity, while activation of NF-κB elevated NFAT transcriptional activity. RCAN1 isoform 4 gene transcription was repressed by its own protein expression in a negative feedback loop. Our findings about RCAN1 gene transcription regulated by NF-κB further supported the vital roles of RCAN1 in cellular functions and its involvement in AD pathogenesis.
钙调神经磷酸酶1调节因子(RCAN1)与神经退行性变和多种癌症的发病机制有关。最近,我们发现RCAN1在唐氏综合征和阿尔茨海默病中表达升高,并且其表达可导致神经元凋亡。由于核因子κB(NF-κB)是参与细胞存活的重要转录因子,而RCAN1在细胞活力中起重要作用,因此我们研究了NF-κB是否调节RCAN1基因表达。我们的结果表明,NF-κB信号可激活RCAN1亚型4基因转录。NF-κB激活了RCAN1亚型4基因启动子。荧光素酶报告基因检测、电泳迁移率变动分析(EMSA)和染色质免疫沉淀法确定了RCAN1亚型4启动子-576-554bp区域存在一个NF-κB反应元件。NF-κB对RCAN1基因表达的激活独立于钙调神经磷酸酶-活化T细胞核因子(calcineurin-NFAT)信号,因为NF-κB反应元件与先前在-350-166bp区域鉴定的NFAT结合位点不同。实际上,钙调神经磷酸酶-NFAT信号的激活降低了NF-κB的转录活性,而NF-κB的激活则提高了NFAT的转录活性。RCAN1亚型4基因转录在负反馈环中受到其自身蛋白表达的抑制。我们关于NF-κB调节RCAN1基因转录的发现进一步支持了RCAN1在细胞功能中的重要作用及其与阿尔茨海默病发病机制的关联。