DDX6与DDX3X相互作用抑制microrna介导的沉默中的翻译。

IF 13.1 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Yanyan Lu,Meng Tao,Hong Su,Yiren Tu,Ji-Ping Wang,Masahiko Kuroda,Xiaozhong Wang
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引用次数: 0

摘要

已知DDX6在microrna介导的沉默中抑制信使RNA (mRNA)翻译并促进mRNA衰变。在胚胎干细胞(ESCs)中,DDX6主要在翻译水平起作用,独立于mRNA的不稳定;然而,DDX6如何抑制翻译的确切分子机制尚不清楚。本研究发现,DDX3X是ESCs中ddx6介导的翻译抑制的一个关键下游靶点。条件敲除DDX3X证明了其在microRNA (miRNA)沉默中的重要作用。生化分析表明,DDX6直接与DDX3X结合,DDX6的c端区域是这种相互作用所必需的。缺乏DDX6的ESCs和DDX6突变体在DDX3X相互作用中存在缺陷的ESCs继续表现出miRNA沉默缺陷。此外,突变体DDX6在体外不能抑制48S预起始复合物的形成。这些发现揭示了DDX6通过与DDX3X的相互作用抑制靶mRNA翻译的新机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DDX6 interacts with DDX3X to repress translation in microRNA-mediated silencing.
DDX6 is known to repress messenger RNA (mRNA) translation and promote mRNA decay in microRNA-mediated silencing. In embryonic stem cells (ESCs), DDX6 primarily functions at the translation level, independent of mRNA destabilization; however, the precise molecular mechanism of how DDX6 represses translation remains unclear. Here, we identify DDX3X as a key downstream target of DDX6-mediated translational repression in ESCs. Conditional knockout of DDX3X demonstrates its essential role in microRNA (miRNA) silencing. Biochemical analyses reveal that DDX6 directly binds to DDX3X, with the C-terminal region of DDX6 being necessary for this interaction. ESCs lacking DDX6 and rescued with a DDX6 mutant that is defective in DDX3X interaction continue to exhibit miRNA silencing defects. Furthermore, the mutant DDX6 is unable to inhibit 48S preinitiation complex formation in vitro. These findings uncover a novel mechanism in which DDX6 represses target mRNA translation via its interaction with DDX3X.
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来源期刊
Nucleic Acids Research
Nucleic Acids Research 生物-生化与分子生物学
CiteScore
27.10
自引率
4.70%
发文量
1057
审稿时长
2 months
期刊介绍: Nucleic Acids Research (NAR) is a scientific journal that publishes research on various aspects of nucleic acids and proteins involved in nucleic acid metabolism and interactions. It covers areas such as chemistry and synthetic biology, computational biology, gene regulation, chromatin and epigenetics, genome integrity, repair and replication, genomics, molecular biology, nucleic acid enzymes, RNA, and structural biology. The journal also includes a Survey and Summary section for brief reviews. Additionally, each year, the first issue is dedicated to biological databases, and an issue in July focuses on web-based software resources for the biological community. Nucleic Acids Research is indexed by several services including Abstracts on Hygiene and Communicable Diseases, Animal Breeding Abstracts, Agricultural Engineering Abstracts, Agbiotech News and Information, BIOSIS Previews, CAB Abstracts, and EMBASE.
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