Zhang Tao, Liu Hehe, Zhou Tianyu, Luo Jun, Wang Jiwen, Han Chunchun, Hu Jiwei, Wu Qianfeng, Wang Yushi
Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, Sichuan Agricultural University, Chengdu, P.R. China.
Cent Eur J Immunol. 2018;43(4):389-398. doi: 10.5114/ceji.2018.81350. Epub 2018 Dec 31.
Interleukin 2 (IL-2), a cytokine, plays an important role in animal immune systems. To investigate the influences of epigenetic modifications on transcription of the duck IL-2 gene, the promoter region of the duck IL-2 gene was cloned. Then, the DNA methylation status of the IL-2 gene promoter (-1337 bp/-924 bp) in immune tissues of ducks was determined using the Sequenom Mass Array methylation technique, and their corresponding expression levels were determined using real-time PCR. The results showed that 2850 bp of the duck IL-2 gene promoter region were obtained. There was one CpG island (-1231 bp/-902 bp) in which 11 CpG sites were distributed. The CpG1 and CpG2 sites are located between the binding sites of NFAT and AP-1, and they had higher homology methylation patterns in different individuals and tissues. The methylation frequencies of 28.5% CpG sites showed negative correlations with the expression levels of the IL-2 mRNA, whereas 71.5% showed positive correlations. These results indicate that the transcription of duck IL-2 may be distinct from that of mammals. CpG1 (-1284 bp) and CpG2 (-1264 bp) in the duck IL-2 promoter showed a higher homology of methylation patterns, indicating a similar regulatory effect on their gene expression, and these CpG sites may be essential for the regulation of transcription of duck IL-2. The methylation pattern of the IL-2 gene promoter in duck was tissue specific.
白细胞介素2(IL-2)作为一种细胞因子,在动物免疫系统中发挥着重要作用。为了研究表观遗传修饰对鸭IL-2基因转录的影响,克隆了鸭IL-2基因的启动子区域。然后,采用Sequenom Mass Array甲基化技术测定鸭免疫组织中IL-2基因启动子(-1337 bp/-924 bp)的DNA甲基化状态,并通过实时荧光定量PCR测定其相应的表达水平。结果表明,获得了鸭IL-2基因启动子区域2850 bp的序列。存在一个CpG岛(-1231 bp/-902 bp),其中分布有11个CpG位点。CpG1和CpG2位点位于NFAT和AP-1的结合位点之间,在不同个体和组织中具有较高的同源甲基化模式。28.5%的CpG位点甲基化频率与IL-2 mRNA表达水平呈负相关,而71.5%呈正相关。这些结果表明,鸭IL-2的转录可能与哺乳动物不同。鸭IL-2启动子中的CpG1(-1284 bp)和CpG2(-1264 bp)显示出较高的甲基化模式同源性,表明它们对基因表达具有相似的调控作用,这些CpG位点可能对鸭IL-2转录调控至关重要。鸭IL-2基因启动子的甲基化模式具有组织特异性。