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AT2细胞中Fbxo45的缺失导致组蛋白供应不足并引发肺腺癌。

Loss of Fbxo45 in AT2 cells leads to insufficient histone supply and initiates lung adenocarcinoma.

作者信息

Li Lian, Li Junya, Chen Ran, Huang Caihu, Zuo Yong, Lu Runhui, Liu Xiaojia, Huang Jiayi, Wang Yanli, Zhao Xian, Cheng Jinke, Zhao Xiaojing, Du Chunling, Yu Jianxiu

机构信息

Department of Biochemistry and Molecular Cell Biology & Department of Thoracic Surgery Ren Ji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China.

Department of Respiratory and Critical Care Medicine, QingPu Branch of Zhongshan Hospital Affiliated to Fudan University, Shanghai, 201700, China.

出版信息

Cell Death Differ. 2024 Dec 13. doi: 10.1038/s41418-024-01433-z.

Abstract

Dysregulation of histone supply is implicated in various cancers, including lung adenocarcinoma (LUAD), although the underlying mechanisms remain poorly understood. Here, we demonstrate that knockout of Fbxo45 in mouse alveolar epithelial type 2 (AT2) cells leads to spontaneous LUAD. Our findings reveal that FBXO45 is a novel cell-cycle-regulated protein that is degraded upon phosphorylation by CDK1 during the S/G2 phase. During the S phase or DNA damage repair, FBXO45 binds to UPF1 and recruits the phosphatase PPP6C, thereby inhibiting UPF1 phosphorylation. This process is crucial for preventing the degradation of replication-dependent (RD) histone mRNAs and ensuring an adequate histone supply. In the absence of FBXO45, the impaired interaction between PPP6C and UPF1 results in sustained hyperphosphorylation of UPF1 throughout the cell cycle, leading to an insufficient histone supply, chromatin relaxation, genomic instability, and an increased rate of gene mutations, ultimately culminating in malignant transformation. Notably, analysis of clinical LUAD specimens confirms a positive correlation between the loss of FBXO45 and genomic instability, which is consistent with our findings in the mouse model. These results highlight the critical role of FBXO45 as a genomic guardian in coordinating histone supply and DNA replication, providing valuable insights into potential therapeutic targets and strategies for the treatment of LUAD.

摘要

组蛋白供应失调与包括肺腺癌(LUAD)在内的多种癌症有关,尽管其潜在机制仍知之甚少。在此,我们证明在小鼠肺泡Ⅱ型(AT2)细胞中敲除Fbxo45会导致自发性LUAD。我们的研究结果表明,FBXO45是一种新型的细胞周期调节蛋白,在S/G2期被CDK1磷酸化后会被降解。在S期或DNA损伤修复过程中,FBXO45与UPF1结合并募集磷酸酶PPP6C,从而抑制UPF1磷酸化。这一过程对于防止复制依赖性(RD)组蛋白mRNA的降解和确保充足的组蛋白供应至关重要。在缺乏FBXO45的情况下,PPP6C与UPF1之间的相互作用受损,导致UPF1在整个细胞周期中持续过度磷酸化,从而导致组蛋白供应不足、染色质松弛、基因组不稳定和基因突变率增加,最终导致恶性转化。值得注意的是,对临床LUAD标本的分析证实FBXO45缺失与基因组不稳定之间呈正相关,这与我们在小鼠模型中的发现一致。这些结果突出了FBXO45作为基因组守护者在协调组蛋白供应和DNA复制中的关键作用,为LUAD的潜在治疗靶点和策略提供了有价值的见解。

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