State Key Laboratory of Oncology in South China and Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, China.
Department of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Piscataway, New Jersey, United States of America.
PLoS Genet. 2021 Nov 18;17(11):e1009899. doi: 10.1371/journal.pgen.1009899. eCollection 2021 Nov.
The robust proliferation of cancer cells requires vastly elevated levels of protein synthesis, which relies on a steady supply of aminoacylated tRNAs. Delivery of tRNAs to the cytoplasm is a highly regulated process, but the machinery for tRNA nuclear export is not fully elucidated. In this study, using a live cell imaging strategy that visualizes nascent transcripts from a specific tRNA gene in yeast, we identified the nuclear basket proteins Mlp1 and Mlp2, two homologs of the human TPR protein, as regulators of tRNA export. TPR expression is significantly increased in lung cancer tissues and correlated with poor prognosis. Consistently, knockdown of TPR inhibits tRNA nuclear export, protein synthesis and cell growth in lung cancer cell lines. We further show that NXF1, a well-known mRNA nuclear export factor, associates with tRNAs and mediates their transport through nuclear pores. Collectively, our findings uncover a conserved mechanism that regulates nuclear export of tRNAs, which is a limiting step in protein synthesis in eukaryotes.
癌细胞的旺盛增殖需要大大提高蛋白质合成水平,这依赖于氨酰化 tRNA 的稳定供应。tRNA 向细胞质的输送是一个高度调控的过程,但 tRNA 核输出的机制尚未完全阐明。在这项研究中,我们使用一种活细胞成像策略,可视化酵母中特定 tRNA 基因的新生转录本,鉴定出核篮蛋白 Mlp1 和 Mlp2,这是人类 TPR 蛋白的两个同源物,是 tRNA 输出的调节剂。TPR 在肺癌组织中的表达显著增加,与预后不良相关。一致地,在肺癌细胞系中敲低 TPR 会抑制 tRNA 核输出、蛋白质合成和细胞生长。我们进一步表明,NXF1,一种著名的 mRNA 核输出因子,与 tRNA 结合,并介导它们通过核孔的运输。总的来说,我们的发现揭示了一种调节 tRNA 核输出的保守机制,这是真核生物蛋白质合成的一个限制步骤。