Atypical E3 ligase ZFP91 promotes small-molecule-induced E2F2 transcription factor degradation for cancer therapy

泛素连接酶 泛素 生物 蛋白质降解 德隆 转录因子 细胞生物学 癌症研究 生物化学 基因
作者
Tingting Liu,Heng Yang,Fang-Fang Zhuo,Zhuo Yang,Meimei Zhao,Qiang Guo,Yang Liu,Dan Liu,Ke‐Wu Zeng,Pengfei Tu
出处
期刊:EBioMedicine [Elsevier BV]
卷期号:86: 104353-104353 被引量:30
标识
DOI:10.1016/j.ebiom.2022.104353
摘要

The E2F family of transcription factors play a crucial role in the development of various cancers. However, E2F members lack targetable binding pockets and are typically considered "undruggable". Unlike canonical small-molecule therapeutics, molecular glues mediate new E3 ligase-protein interactions to induce selective proteasomal degradation, which represents an attractive option to overcome these limitations.Human proteome microarray was utilized to identify a natural product-derived molecular glue for targeting E2F2 degradation. Co-IP analysis with stable isotope labeling of amino acids in cell culture (SILAC)-based quantitative proteomics was carried out to further explore the E3 ligase for E2F2 degradation.In this study, we identified a molecular glue bufalin, which significantly promoted E2F2 degradation. Unexpectedly, E2F2 underwent ubiquitination and proteasomal degradation via a previously undisclosed atypical E3 ligase, zinc finger protein 91 (ZFP91). In particular, we observed that bufalin markedly promoted E2F2-ZFP91 complex formation, thereby leading to E2F2 polyubiquitination via K48-linked ubiquitin chains for degradation. E2F2 degradation subsequently caused transcriptional suppression of multiple oncogenes including c-Myc, CCNE1, CCNE2, MCM5 and CDK1, and inhibited hepatocellular carcinoma growth in vitro and in vivo.Collectively, our findings open up a new direction for transcription factors degradation by targeting atypical E3 ligase ZFP91. Meanwhile, the chemical knockdown strategy with molecular glue may promote innovative transcription factor degrader development in cancer therapy.This work was financially supported by the National Key Research and Development Project of China (2022YFC3501601), National Natural Sciences Foundation of China (81973505, 82174008, 82030114), and China Postdoctoral Science Foundation (2019M650396), the Fundamental Research Funds for the Central Universities.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
123发布了新的文献求助10
1秒前
GeneYang完成签到 ,获得积分10
1秒前
领导范儿应助aaa采纳,获得10
2秒前
bingobigtree完成签到,获得积分10
2秒前
3yr发布了新的文献求助10
2秒前
3秒前
千空发布了新的文献求助10
4秒前
陶以沫发布了新的文献求助10
4秒前
量子星尘发布了新的文献求助10
5秒前
Amjd发布了新的文献求助10
6秒前
许燕飞关注了科研通微信公众号
6秒前
7秒前
LIJIngcan发布了新的文献求助10
7秒前
羽蒙完成签到,获得积分20
7秒前
高贵南风完成签到,获得积分10
7秒前
8秒前
科研民工_郭完成签到,获得积分10
9秒前
10秒前
10秒前
123完成签到,获得积分10
11秒前
桐桐应助千空采纳,获得10
11秒前
zz完成签到,获得积分10
12秒前
深情安青应助Humble采纳,获得10
12秒前
12秒前
gaoyuan完成签到,获得积分10
13秒前
13秒前
13秒前
13秒前
共享精神应助Aterna春采纳,获得10
13秒前
aaa发布了新的文献求助10
14秒前
毛毛洁发布了新的文献求助10
15秒前
16秒前
16秒前
嘻嘻应助云泽采纳,获得10
17秒前
18秒前
George发布了新的文献求助10
19秒前
bingobigtree发布了新的文献求助10
19秒前
陶以沫完成签到,获得积分10
19秒前
LZNL完成签到,获得积分10
19秒前
高分求助中
【提示信息,请勿应助】请使用合适的网盘上传文件 10000
Continuum Thermodynamics and Material Modelling 2000
Chinesen in Europa – Europäer in China: Journalisten, Spione, Studenten 1200
Deutsche in China 1920-1950 1200
Electron microscopy study of magnesium hydride (MgH2) for Hydrogen Storage 800
Green Star Japan: Esperanto and the International Language Question, 1880–1945 800
Sentimental Republic: Chinese Intellectuals and the Maoist Past 800
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3870874
求助须知:如何正确求助?哪些是违规求助? 3412925
关于积分的说明 10682149
捐赠科研通 3137423
什么是DOI,文献DOI怎么找? 1730915
邀请新用户注册赠送积分活动 834476
科研通“疑难数据库(出版商)”最低求助积分说明 781172