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无翅(Wingless)和盘域(Archipelago),一个果蝇 E3 泛素连接酶和人类肿瘤抑制因子 FBW7 的同源物,在翅膀发育中表现出拮抗关系。

Wingless and Archipelago, a fly E3 ubiquitin ligase and a homolog of human tumor suppressor FBW7, show an antagonistic relationship in wing development.

机构信息

Department of Biological Sciences, Korea Advanced Institute of Science and Technology, 291 Daehak-ro, Yuseong-gu, Daejeon, Korea.

出版信息

BMC Dev Biol. 2020 Jun 29;20(1):14. doi: 10.1186/s12861-020-00217-1.

Abstract

BACKGROUND

Archipelago (Ago) is a Drosophila homolog of mammalian F-box and WD repeat domain-containing 7 (FBW7, also known as FBXW7). In previous studies, FBW7 has been addressed as a tumor suppressor mediating ubiquitin-dependent proteolysis of several oncogenic proteins. Ubiquitination is a type of protein modification that directs protein for degradation as well as sorting. The level of beta-catenin (β-cat), an intracellular signal transducer in Wnt signaling pathway, is reduced upon overexpression of FBW7 in human cancer cell lines. Loss of function mutations in FBW7 and overactive Wnt signaling have been reported to be responsible for human cancers.

RESULTS

We found that Ago is important for the formation of shafts in chemosensory bristles at wing margin. This loss of shaft phenotype by knockdown of ago was rescued by knockdown of wingless (wg) whereas wing notching phenotype by knockdown of wg was rescued by knockdown of ago, establishing an antagonistic relationship between ago and wg. In line with this finding, knockdown of ago increased the level of Armadillo (Arm), a homolog of β-cat, in Drosophila tissue. Furthermore, knockdown of ago increased the level of Distal-less (Dll) and extracellular Wg in wing discs. In S2 cells, the amount of secreted Wg was increased by knockdown of Ago but decreased by Ago overexpression. Therefore, Ago plays a previously unidentified role in the inhibition of Wg secretion. Ago-overexpressing clones in wing discs exhibited accumulation of Wg in endoplasmic reticulum (ER), suggesting that Ago prevents Wg protein from moving to Golgi from ER.

CONCLUSIONS

We concluded that Ago plays dual roles in inhibiting Wg signaling. First, Ago decreases the level of Arm, by which Wg signaling is downregulated in Wg-responding cells. Second, Ago decreases the level of extracellular Wg by inhibiting movement of Wg from ER to Golgi in Wg-producing cells.

摘要

背景

果蝇的同源物 Archipelago(Ago)是一种哺乳动物 F-box 和 WD 重复结构域蛋白 7(FBW7,也称为 FBXW7)。在之前的研究中,FBW7 被认为是一种肿瘤抑制因子,通过泛素依赖性蛋白水解作用来调节几种致癌蛋白。泛素化是一种蛋白质修饰,可指导蛋白质降解和分类。在人类癌细胞系中过表达 FBW7 会降低细胞内信号转导蛋白 Wnt 信号通路中的β-连环蛋白(β-cat)的水平。已经报道 FBW7 的功能丧失突变和过度活跃的 Wnt 信号与人类癌症有关。

结果

我们发现 Ago 对于翅膀边缘的化学感觉刚毛轴的形成很重要。ago 敲低导致的轴缺失表型可以通过 wg 敲低来挽救,而 wg 敲低导致的翅膀缺口表型可以通过 ago 敲低来挽救,这表明 ago 和 wg 之间存在拮抗关系。与这一发现一致的是,ago 敲低增加了果蝇组织中 Armadillo(β-cat 的同源物)的水平。此外,ago 敲低增加了 wing discs 中 Distal-less(Dll)和细胞外 Wg 的水平。在 S2 细胞中,通过敲低 Ago 增加了分泌型 Wg 的量,但通过 Ago 过表达降低了分泌型 Wg 的量。因此,Ago 在抑制 Wg 分泌中发挥了以前未被识别的作用。在 wing discs 中,Ago 过表达克隆表现出 Wg 在内质网(ER)中的积累,表明 Ago 阻止 Wg 蛋白从 ER 移动到高尔基体。

结论

我们得出结论,Ago 在抑制 Wg 信号传导中发挥双重作用。首先,Ago 通过降低 Wg 反应细胞中 Wg 信号的 Arm 水平来发挥作用。其次,Ago 通过抑制 Wg 从 ER 到高尔基体的运动来降低细胞外 Wg 的水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c74/7322864/e101976a5701/12861_2020_217_Fig1_HTML.jpg

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