St-Patrick Research Group in Basic Oncology, Centre Hospitalier Universitaire de Québec-Université Laval Research Center, L'Hôtel-Dieu de Québec, Québec City, Canada
Laval University Cancer Research Centre, Québec City, Canada.
Life Sci Alliance. 2020 Mar 11;3(4). doi: 10.26508/lsa.201900632. Print 2020 Apr.
In animals, miRNAs are the most prevalent small non-coding RNA molecules controlling posttranscriptional gene regulation. The Argonaute proteins (AGO) mediate miRNA-guided gene silencing by recruiting multiple factors involved in translational repression, deadenylation, and decapping. Here, we report that CSDE1, an RNA-binding protein linked to stem cell maintenance and metastasis in cancer, interacts with AGO2 within miRNA-induced silencing complex and mediates gene silencing through its N-terminal domains. We show that CSDE1 interacts with LSM14A, a constituent of P-body assembly and further associates to the DCP1-DCP2 decapping complex, suggesting that CSDE1 could promote the decay of miRNA-induced silencing complex-targeted mRNAs. Together, our findings uncover a hitherto unknown mechanism used by CSDE1 in the control of gene expression mediated by the miRNA pathway.
在动物中,miRNA 是最普遍的小非编码 RNA 分子,可控制转录后基因调控。Argonaute 蛋白(AGO)通过招募多个参与翻译抑制、去腺苷酸化和脱帽的因子来介导 miRNA 指导的基因沉默。在这里,我们报告称,与癌症中的干细胞维持和转移有关的 RNA 结合蛋白 CSDE1 与 miRNA 诱导的沉默复合物中的 AGO2 相互作用,并通过其 N 端结构域介导基因沉默。我们表明 CSDE1 与 LSM14A 相互作用,LSM14A 是 P 体组装的组成部分,进一步与 DCP1-DCP2 脱帽复合物相关联,表明 CSDE1 可以促进 miRNA 诱导的沉默复合物靶向 mRNA 的降解。总之,我们的发现揭示了 CSDE1 在 miRNA 通路介导的基因表达控制中使用的一种迄今未知的机制。