Suppr超能文献

CSDE1 减弱 microRNA 介导的 PMEPA1 在黑色素瘤中的沉默作用。

CSDE1 attenuates microRNA-mediated silencing of PMEPA1 in melanoma.

机构信息

CHU de Québec-Université Laval Research Center (Oncology Division), Québec, QC, Canada.

Université Laval Cancer Research Centre, Québec, QC, Canada.

出版信息

Oncogene. 2021 May;40(18):3231-3244. doi: 10.1038/s41388-021-01767-9. Epub 2021 Apr 8.

Abstract

MicroRNAs and RNA-binding proteins (RBPs) primarily target the 3' UTR of mRNAs to control their translation and stability. However, their co-regulatory effects on specific mRNAs in physiology and disease are yet to be fully explored. CSDE1 is an RBP that promotes metastasis in melanoma and mechanisms underlying its oncogenic activities need to be completely defined. Here we report that CSDE1 interacts with specific miRNA-induced silencing complexes (miRISC) in melanoma. We find an association of CSDE1 with AGO2, the essential component of miRISC, which is facilitated by target mRNAs and depends on the first cold shock domain of CSDE1. Both CSDE1 and AGO2 bind to 3' UTR of PMEPA1. CSDE1 counters AGO2 binding, leading to an increase of PMEPA1 expression. We also identify a miRNA, miR-129-5p, that represses PMEPA1 expression in melanoma. Collectively, our results show that PMEPA1 promotes tumorigenic traits and that CSDE1 along with miR-129-5p/AGO2 miRISC act antagonistically to fine-tune PMEPA1 expression toward the progression of melanoma.

摘要

微小 RNA 与 RNA 结合蛋白 (RBPs) 主要靶向 mRNAs 的 3'UTR,以控制其翻译和稳定性。然而,它们在生理和疾病中的特定 mRNAs 上的共同调节作用尚未得到充分探索。CSDE1 是一种在黑色素瘤中促进转移的 RBP,其致癌活性的机制需要完全定义。在这里,我们报告 CSDE1 与黑色素瘤中的特定 miRNA 诱导的沉默复合物 (miRISC) 相互作用。我们发现 CSDE1 与 miRISC 的必需成分 AGO2 之间存在关联,这是由靶 mRNAs 促进的,并取决于 CSDE1 的第一个冷休克结构域。CSDE1 和 AGO2 都结合到 PMEPA1 的 3'UTR。CSDE1 拮抗 AGO2 结合,导致 PMEPA1 表达增加。我们还鉴定了一种 miRNA,miR-129-5p,它在黑色素瘤中抑制 PMEPA1 的表达。总的来说,我们的结果表明 PMEPA1 促进了致瘤特性,CSDE1 与 miR-129-5p/AGO2 miRISC 一起拮抗作用,精细调节 PMEPA1 的表达,从而促进黑色素瘤的进展。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验