Department of Molecular Biology, Institute for Biological Research, University of Belgrade, Belgrade, Serbia.
J Cell Mol Med. 2019 Apr;23(4):2610-2618. doi: 10.1111/jcmm.14154. Epub 2019 Jan 29.
Poly [ADP-ribose] polymerase 1 (PARP-1) has an inhibitory effect on C-X-C motif chemokine 12 gene (Cxcl12) transcription. We examined whether PARP-1 affects the epigenetic control of Cxcl12 expression by changing its DNA methylation pattern. We observed increased expression of Cxcl12 in PARP-1 knock-out mouse embryonic fibroblasts (PARP1-/-) in comparison to wild-type mouse embryonic fibroblasts (NIH3T3). In the Cxcl12 gene, a CpG island is present in the promoter, the 5' untranslated region (5' UTR), the first exon and in the first intron. The methylation state of Cxcl12 in each cell line was investigated by methylation-specific PCR (MSP) and high resolution melting analysis (HRM). Both methods revealed strong demethylation in PARP1-/- compared to NIH3T3 cells in all four DNA regions. Increased expression of the Ten-eleven translocation (Tet) genes in PARP1-/- cells indicated that TETs could be important factors in Cxcl12 demethylation in the absence of PARP-1, accounting for its increased expression. Our results showed that PARP-1 was a potential upstream player in (de)methylation events that modulated Cxcl12 expression.
聚[ADP-核糖]聚合酶 1(PARP-1)对 C-X-C 基序趋化因子 12 基因(Cxcl12)的转录具有抑制作用。我们研究了 PARP-1 是否通过改变其 DNA 甲基化模式来影响 Cxcl12 表达的表观遗传控制。与野生型小鼠胚胎成纤维细胞(NIH3T3)相比,我们观察到 PARP-1 敲除小鼠胚胎成纤维细胞(PARP1-/-)中 Cxcl12 的表达增加。在 Cxcl12 基因中,启动子、5'非翻译区(5'UTR)、第一外显子和第一内含子中存在一个 CpG 岛。通过甲基化特异性 PCR(MSP)和高分辨率熔解分析(HRM)研究了每种细胞系中 Cxcl12 的甲基化状态。这两种方法都显示 PARP1-/- 细胞中 Cxcl12 的甲基化程度明显低于 NIH3T3 细胞,在四个 DNA 区域均如此。PARP1-/- 细胞中 Ten-eleven 易位(Tet)基因的表达增加表明,TET 可能是 PARP-1 缺失时 Cxcl12 去甲基化的重要因素,这解释了其表达增加。我们的研究结果表明,PARP-1 可能是调节 Cxcl12 表达的(去)甲基化事件的上游调控因子。