The Key Laboratory of Cell Proliferation and Regulation Biology, Ministry of Education, Institute of Cell Biology, College of Life Sciences, Beijing Normal University, Beijing, China.
The Key Laboratory of Cell Proliferation and Regulation Biology, Ministry of Education, Institute of Cell Biology, College of Life Sciences, Beijing Normal University, Beijing, China; Academy of Plateau Science and Sustainability, People's Government of Qinghai Province & Beijing Normal University, Xining, China.
J Biol Chem. 2020 Dec 25;295(52):18134-18147. doi: 10.1074/jbc.RA119.012009. Epub 2020 Oct 22.
NSun2 is an RNA methyltransferase introducing 5-methylcytosine into tRNAs, mRNAs, and noncoding RNAs, thereby influencing the levels or function of these RNAs. Autotaxin (ATX) is a secreted glycoprotein and is recognized as a key factor in converting lysophosphatidylcholine into lysophosphatidic acid (LPA). The ATX-LPA axis exerts multiple biological effects in cell survival, migration, proliferation, and differentiation. Here, we show that NSun2 is involved in the regulation of cell migration through methylating ATX mRNA. In the human glioma cell line U87, knockdown of NSun2 decreased ATX protein levels, whereas overexpression of NSun2 elevated ATX protein levels. However, neither overexpression nor knockdown of NSun2 altered ATX mRNA levels. Further studies revealed that NSun2 methylated the 3'-UTR of ATX mRNA at cytosine 2756 and Methylation by NSun2 enhanced ATX mRNA translation. In addition, NSun2-mediated 5-methylcytosine methylation promoted the export of ATX mRNA from nucleus to cytoplasm in an ALYREF-dependent manner. Knockdown of NSun2 suppressed the migration of U87 cells, which was rescued by the addition of LPA. In summary, we identify NSun2-mediated methylation of ATX mRNA as a novel mechanism in the regulation of ATX.
NSun2 是一种 RNA 甲基转移酶,它将 5-甲基胞嘧啶引入 tRNA、mRNA 和非编码 RNA 中,从而影响这些 RNA 的水平或功能。自分泌酶 (ATX) 是一种分泌型糖蛋白,被认为是将溶血磷脂酰胆碱转化为溶血磷脂酸 (LPA) 的关键因素。ATX-LPA 轴在细胞存活、迁移、增殖和分化中发挥多种生物学效应。在这里,我们表明 NSun2 通过甲基化 ATX mRNA 参与调节细胞迁移。在人神经胶质瘤细胞系 U87 中,敲低 NSun2 降低了 ATX 蛋白水平,而过表达 NSun2 则提高了 ATX 蛋白水平。然而,过表达或敲低 NSun2 均未改变 ATX mRNA 水平。进一步的研究表明,NSun2 在 ATX mRNA 的 3'-UTR 上的胞嘧啶 2756 处甲基化,并增强了 ATX mRNA 的翻译。此外,NSun2 介导的 5-甲基胞嘧啶甲基化以 ALYREF 依赖性的方式促进 ATX mRNA 从细胞核输出到细胞质。敲低 NSun2 抑制了 U87 细胞的迁移,而添加 LPA 则挽救了这一现象。综上所述,我们确定了 NSun2 介导的 ATX mRNA 甲基化是调节 ATX 的一种新机制。