State Key Laboratory of Biocontrol, School of Life Science, Sun Yat-Sen University, Guangzhou, People's Republic of China.
Mol Genet Genomics. 2010 Sep;284(3):185-95. doi: 10.1007/s00438-010-0558-z. Epub 2010 Jul 17.
Tumor necrosis factor alpha-induced protein 8-like 2 (TNFAIP8L2) is a new member of the tumor necrosis factor-alpha-induced protein 8 (TNFAIP8) family that functions as an important factor in the maintenance of immune homeostasis. In this study, we cloned the cDNA sequences and analyzed the genomic structure of porcine TNFAIP8L2. RH mapping using the IMpRH panel showed that this gene was closely linked to microsatellite marker SW512 in pig chromosome 4. Subcellular localization analysis showed GFP-TNFAIP8L2 fusion protein distributed in nucleus as well as cytoplasm including mitochondria and endoplasmic reticulum. Real-time PCR analysis revealed that porcine TNFAIP8L2 was more highly expressed in spleen than other tissues. To understand its characterization of transcriptional regulation, we cloned approximately 2 kb of 5'-regulatory region upstream to the porcine TNFAIP8L2 translational start site and generated sequential deletion constructs evaluated in dual-luciferase reporter assay. The results demonstrated that its core promoter is 435 base pairs (bp) upstream to the transcription initiation site. Then, site-directed mutation experiment combined with electrophoretic mobility shift assay (EMSA) indicated that M-CAT binding factor (MCBF) and activator protein 1 (AP-1) were important transcription factors for porcine TNFAIP8L2. These findings provide an important basis for further understanding of porcine TNFAIP8L2 regulation and function in swine.
肿瘤坏死因子-α诱导蛋白 8 样蛋白 2(TNFAIP8L2)是肿瘤坏死因子-α诱导蛋白 8(TNFAIP8)家族的新成员,作为维持免疫稳态的重要因素发挥作用。在本研究中,我们克隆了猪 TNFAIP8L2 的 cDNA 序列并分析了其基因组结构。使用 IMpRH 面板进行 RH 图谱定位表明,该基因与猪 4 号染色体上的微卫星标记 SW512 紧密连锁。亚细胞定位分析表明 GFP-TNFAIP8L2 融合蛋白分布在细胞核以及细胞质中,包括线粒体和内质网。实时 PCR 分析显示,猪 TNFAIP8L2 在脾脏中的表达水平高于其他组织。为了了解其转录调控的特征,我们克隆了猪 TNFAIP8L2 翻译起始位点上游约 2kb 的 5'-调控区,并生成了在双荧光素酶报告基因检测中的连续缺失构建体。结果表明,其核心启动子位于转录起始位点上游 435 个碱基对(bp)。然后,定点突变实验结合电泳迁移率变动分析(EMSA)表明,M-CAT 结合因子(MCBF)和激活蛋白 1(AP-1)是猪 TNFAIP8L2 的重要转录因子。这些发现为进一步了解猪 TNFAIP8L2 在猪中的调控和功能提供了重要基础。