Department of Obstetrics and Gynecology, School of Medicine, International Peace Maternity and Child Health Hospital, Shanghai Jiao Tong University, Shanghai, China.
Department of Obstetrics and Gynecology, Jiangwan Hospital of Shanghai Hongkou District, Shanghai, China.
J Cell Mol Med. 2019 May;23(5):3202-3213. doi: 10.1111/jcmm.14179. Epub 2019 Mar 18.
Preeclampsia (PE) is a major cause of mortality and morbidity among pregnant mothers and their fetuses worldwide. Recent studies have shown that several microRNAs (miRNAs) play crucial role in pathogenesis of PE patients; however, the mechanisms responsible for differences in miRNA function in PE largely remain to be determined.
We studied that NUDT21 expression was markedly increased, whereas EZH2 was decreased in placental samples from patients with PE. We identified NUDT21 as an interaction partner of enhancer of zeste homologue 2 (EZH2). NUDT21 co-localized with EZH2 in the human trophoblast cell line, HTR-8/SVneo and NUDT21 was shown to bind to EZH2 in RNA immunoprecipitation assays. NUDT21 has previously been reported to be involved in alternative polyadenylation; thus, the interaction between NUDT21 and EZH2 may play an important role in the crosstalk between alternative polyadenylation (APA) and miRNA-mediated gene silencing in PE.
In the human trophoblast cell line HTR-8/SVneo, loss-of-function assays indicated that knockdown of NUDT21 suppressed cell proliferation, migration and tube formation. Furthermore, functional studies showed that NUDT21 elongated the 3'-UTR of mRNAs thereby exposing more miRNA binding sites (including miR138 and miR363), which enhanced the efficiency of miRNA-mediated gene silencing and promoted EZH2 binding.
This is the first report about the relationship of NUDT21 and EZH2. The data indicate that the aberrant expression of NUDT21 contributes to PE by targeting 3'-UTR of EZH2 mRNA. These findings may provide novel targets for future investigations into therapeutic strategies for PE.
子痫前期(PE)是全球孕产妇及其胎儿死亡和发病的主要原因。最近的研究表明,几种 microRNA(miRNA)在 PE 患者的发病机制中发挥关键作用;然而,导致 miRNA 功能差异的机制在很大程度上仍有待确定。
我们研究了 NUDT21 在 PE 患者胎盘样本中的表达明显增加,而 EZH2 则减少。我们确定 NUDT21 是增强子的同系物 2(EZH2)的相互作用伙伴。NUDT21 在人滋养细胞系 HTR-8/SVneo 中与 EZH2 共定位,并且在 RNA 免疫沉淀测定中显示 NUDT21 与 EZH2 结合。NUDT21 先前已被报道参与可变多聚腺苷酸化;因此,NUDT21 和 EZH2 之间的相互作用可能在可变多聚腺苷酸化(APA)和 miRNA 介导的基因沉默之间的串扰中发挥重要作用。
在人滋养细胞系 HTR-8/SVneo 中,功能丧失实验表明,NUDT21 的敲低抑制细胞增殖、迁移和管形成。此外,功能研究表明,NUDT21 延长了 mRNA 的 3'-UTR,从而暴露了更多的 miRNA 结合位点(包括 miR138 和 miR363),这增强了 miRNA 介导的基因沉默效率,并促进了 EZH2 结合。
这是关于 NUDT21 和 EZH2 之间关系的第一份报告。数据表明,NUDT21 的异常表达通过靶向 EZH2 mRNA 的 3'-UTR 导致 PE。这些发现可能为未来针对 PE 的治疗策略的研究提供新的靶点。