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真核起始因子 4A3 抑制 Wnt/β-catenin 信号通路并调节斑马鱼胚胎体轴形成。

Eukaryotic initiation factor 4A3 inhibits Wnt/β-catenin signaling and regulates axis formation in zebrafish embryos.

机构信息

Key Laboratory of Marine Drugs (Ocean University of China), Chinese Ministry of Education, and School of Medicine and Pharmacy, Ocean University of China, 5 Yushan Road, Qingdao 266003, China.

Laboratory for Marine Drugs and Bioproducts, Pilot National Laboratory for Marine Science and Technology (Qingdao), Qingdao 266003, China.

出版信息

Development. 2021 May 1;148(9). doi: 10.1242/dev.198101. Epub 2021 Apr 29.

Abstract

A key step in the activation of canonical Wnt signaling is the interaction between β-catenin and Tcf/Lefs that forms the transcription activation complex and facilitates the expression of target genes. Eukaryotic initiation factor 4A3 (EIF4A3) is an ATP-dependent DEAD box-family RNA helicase and acts as a core subunit of the exon junction complex (EJC) to control a series of RNA post-transcriptional processes. In this study, we uncover that EIF4A3 functions as a Wnt inhibitor by interfering with the formation of β-catenin/Tcf transcription activation complex. As Wnt stimulation increases, accumulated β-catenin displaces EIF4A3 from a transcriptional complex with Tcf/Lef, allowing the active complex to facilitate the expression of target genes. In zebrafish embryos, eif4a3 depletion inhibited the development of the dorsal organizer and pattern formation of the anterior neuroectoderm by increasing Wnt/β-catenin signaling. Conversely, overexpression of eif4a3 decreased Wnt/β-catenin signaling and inhibited the formation of the dorsal organizer before gastrulation. Our results reveal previously unreported roles of EIF4A3 in the inhibition of Wnt signaling and the regulation of embryonic development in zebrafish.

摘要

经典 Wnt 信号通路激活的关键步骤是β-连环蛋白与 Tcf/Lef 的相互作用,这种相互作用形成转录激活复合物,并促进靶基因的表达。真核起始因子 4A3(EIF4A3)是一种依赖于 ATP 的 DEAD 盒家族 RNA 解旋酶,作为外显子连接复合物(EJC)的核心亚基,可控制一系列 RNA 转录后过程。在本研究中,我们揭示了 EIF4A3 通过干扰β-连环蛋白/Tcf 转录激活复合物的形成,发挥 Wnt 抑制剂的作用。随着 Wnt 刺激的增加,积累的β-连环蛋白将 EIF4A3 从与 Tcf/Lef 的转录复合物中置换出来,使活性复合物能够促进靶基因的表达。在斑马鱼胚胎中,eif4a3 耗尽通过增加 Wnt/β-连环蛋白信号来抑制背侧组织者的发育和前神经外胚层的模式形成。相反,eif4a3 的过表达在原肠胚形成前降低了 Wnt/β-连环蛋白信号,并抑制了背侧组织者的形成。我们的研究结果揭示了 EIF4A3 在抑制 Wnt 信号和调控斑马鱼胚胎发育中的以前未报道的作用。

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