Department of Biology and Chemistry, College of Sciences, National University of Defense Technology, Changsha, 410073, Hunan, China.
Key Laboratory of Elemene Class Anti-Cancer Chinese Medicine of Zhejiang Province, Hangzhou Normal University, Hangzhou, 311121, Zhejiang, China.
Biol Direct. 2022 Jul 13;17(1):17. doi: 10.1186/s13062-022-00331-z.
RNF8 is an E3 ligase identified as a critical DNA damage-responsive protein. Recently, multiple reports have shown that RNF8 could be used as an important therapeutic target for cancer chemo/radiotherapy. However, the understanding of RNF8 remains limited due to the lack of its interactome reference map and comprehensive analysis of RNF8 in diverse cancers, which underscores the need to map the interactome of RNF8 via high-throughput methods.
A two-way identification method based on LC-MS was designed for the identification of the RNF8 interactome with high-specificity. By in silico analysis and in vitro validation, we identified a new reference map of the RNF8 interactome network containing many new targets, such as YBX1, DNMT1, and HDCA1, new biological functions and the gene-disease associations of RNF8. Our results revealed a close relationship between RNF8 and neurodegenerative diseases or tumor-infiltrating immune cells using bulk RNA-seq and scRNA-seq datasets. As a proof of concept of our interactome map, we validated the direct binding between RNF8 and YBX1 and showed that RNF8 catalyzed the ubiquitination of YBX1. These results demonstrated that RNF8 might be a crucial regulator of YBX1.
Our work provides a unique framework for researchers and clinicians who seek to better explore or understand RNF8-regulated biological functions in cancers. This study will hopefully facilitate the rational design and further development of anti-RNF8 therapy in cancers.
RNF8 是一种 E3 连接酶,被认为是一种关键的 DNA 损伤反应蛋白。最近,多项研究表明,RNF8 可以作为癌症化疗/放疗的重要治疗靶点。然而,由于缺乏其相互作用参考图谱和对不同癌症中 RNF8 的综合分析,对 RNF8 的认识仍然有限,这凸显了通过高通量方法绘制 RNF8 相互作用图谱的必要性。
我们设计了一种基于 LC-MS 的双向鉴定方法,用于鉴定具有高特异性的 RNF8 相互作用组。通过计算机分析和体外验证,我们确定了 RNF8 相互作用组网络的新参考图谱,其中包含许多新的靶标,如 YBX1、DNMT1 和 HDCA1,以及 RNF8 的新生物学功能和基因-疾病关联。我们的结果使用批量 RNA-seq 和 scRNA-seq 数据集揭示了 RNF8 与神经退行性疾病或肿瘤浸润免疫细胞之间的密切关系。作为我们相互作用组图谱的概念验证,我们验证了 RNF8 和 YBX1 之间的直接结合,并表明 RNF8 催化了 YBX1 的泛素化。这些结果表明 RNF8 可能是 YBX1 的关键调节因子。
我们的工作为寻求更好地探索或理解癌症中 RNF8 调节的生物学功能的研究人员和临床医生提供了一个独特的框架。这项研究有望促进癌症中针对 RNF8 的合理设计和进一步发展。