Cai Tao, Hirai Hiroki, Xu Huanyu, Notkins Abner L
Experimental Medicine Section, Laboratory of Sensory Biology, National Institute of Dental and Craniofacial Research (NIDCR), National Institutes of Health (NIH), B30/Rm106, Bethesda, MD, 20892, USA,
Acta Diabetol. 2015 Jun;52(3):573-80. doi: 10.1007/s00592-014-0689-5. Epub 2014 Dec 21.
IA-2 is a transmembrane protein found in the dense-core vesicles (DCV) of neuroendocrine cells and one of the major autoantigens in type 1 diabetes. DCV are involved in the secretion of hormones (e.g., insulin) and neurotransmitters. Stimulation of pancreatic β cells with glucose upregulates the expression of IA-2 and an increase in IA-2 results in an increase in the number of DCV. Little is known, however, about the promoter region of IA-2 or the transcriptional factors that regulate the expression of this gene.
In the present study, we constructed eight deletion fragments from the upstream region of the IA-2 transcription start site and linked them to a luciferase reporter.
By this approach, we have identified a short bp region (-216 to +115) that has strong promoter activity. We also identified a transcription factor, cAMP responsive element-binding protein (CREB), which binds to two CREB-related binding sites located in this region. The binding of CREB to these sites enhanced IA-2 transcription by more than fivefold. We confirmed these findings by site-directed mutagenesis, chromatin immunoprecipitation assays and RNAi inhibition.
Based on these findings, we conclude that the PKA pathway is a critical, but not the exclusive signaling pathway involved in IA-2 gene expression.
IA-2是一种跨膜蛋白,存在于神经内分泌细胞的致密核心囊泡(DCV)中,是1型糖尿病的主要自身抗原之一。DCV参与激素(如胰岛素)和神经递质的分泌。用葡萄糖刺激胰腺β细胞会上调IA-2的表达,IA-2的增加会导致DCV数量增加。然而,关于IA-2的启动子区域或调节该基因表达的转录因子知之甚少。
在本研究中,我们从IA-2转录起始位点的上游区域构建了八个缺失片段,并将它们与荧光素酶报告基因相连。
通过这种方法,我们鉴定出一个具有强启动子活性的短bp区域(-216至+115)。我们还鉴定出一种转录因子,即环磷酸腺苷反应元件结合蛋白(CREB),它与位于该区域的两个CREB相关结合位点结合。CREB与这些位点的结合使IA-2转录增强了五倍以上。我们通过定点诱变、染色质免疫沉淀试验和RNAi抑制证实了这些发现。
基于这些发现,我们得出结论,蛋白激酶A途径是参与IA-2基因表达的关键但非唯一信号通路。