Department of Cancer Biology, Dana Farber Cancer Institute, 250 Longwood Avenue, Boston, Massachusetts 02115, USA.
Nature. 2012 May 2;485(7396):109-13. doi: 10.1038/nature11083.
The mTOR complex 1 (mTORC1) kinase nucleates a pathway that promotes cell growth and proliferation and is the target of rapamycin, a drug with many clinical uses. mTORC1 regulates messenger RNA translation, but the overall translational program is poorly defined and no unifying model exists to explain how mTORC1 differentially controls the translation of specific mRNAs. Here we use high-resolution transcriptome-scale ribosome profiling to monitor translation in mouse cells acutely treated with the mTOR inhibitor Torin 1, which, unlike rapamycin, fully inhibits mTORC1 (ref. 2). Our data reveal a surprisingly simple model of the mRNA features and mechanisms that confer mTORC1-dependent translation control. The subset of mRNAs that are specifically regulated by mTORC1 consists almost entirely of transcripts with established 5' terminal oligopyrimidine (TOP) motifs, or, like Hsp90ab1 and Ybx1, with previously unrecognized TOP or related TOP-like motifs that we identified. We find no evidence to support proposals that mTORC1 preferentially regulates mRNAs with increased 5' untranslated region length or complexity. mTORC1 phosphorylates a myriad of translational regulators, but how it controls TOP mRNA translation is unknown. Remarkably, loss of just the 4E-BP family of translational repressors, arguably the best characterized mTORC1 substrates, is sufficient to render TOP and TOP-like mRNA translation resistant to Torin 1. The 4E-BPs inhibit translation initiation by interfering with the interaction between the cap-binding protein eIF4E and eIF4G1. Loss of this interaction diminishes the capacity of eIF4E to bind TOP and TOP-like mRNAs much more than other mRNAs, explaining why mTOR inhibition selectively suppresses their translation. Our results clarify the translational program controlled by mTORC1 and identify 4E-BPs and eIF4G1 as its master effectors.
雷帕霉素靶蛋白复合物 1(mTORC1)激酶是促进细胞生长和增殖的途径的核心,它是雷帕霉素的靶标,雷帕霉素是一种具有多种临床用途的药物。mTORC1 调节信使 RNA 翻译,但整体翻译程序定义不明确,也没有统一的模型来解释 mTORC1 如何差异调控特定 mRNAs 的翻译。在这里,我们使用高分辨率转录组规模核糖体谱来监测急性用 mTOR 抑制剂 Torin 1 处理的小鼠细胞中的翻译,与雷帕霉素不同,Torin 1 完全抑制 mTORC1(参考文献 2)。我们的数据揭示了一个令人惊讶的简单模型,说明了赋予 mTORC1 依赖性翻译控制的 mRNA 特征和机制。几乎完全由具有既定 5'端寡嘧啶(TOP)基序的 mRNAs 组成的 mTORC1 特异性调控的 mRNA 子集,或者像 Hsp90ab1 和 Ybx1 一样,具有我们发现的以前未被识别的 TOP 或相关的 TOP 样基序。我们没有证据支持 mTORC1 优先调控具有增加的 5'非翻译区长度或复杂性的 mRNAs 的建议。mTORC1 磷酸化了大量的翻译调节剂,但它如何控制 TOP mRNA 翻译尚不清楚。值得注意的是,仅失去翻译抑制剂 4E-BP 家族,这可能是最具特征的 mTORC1 底物,足以使 TOP 和 TOP 样 mRNA 翻译对 Torin 1 产生抗性。4E-BPs 通过干扰帽结合蛋白 eIF4E 与 eIF4G1 之间的相互作用来抑制翻译起始。这种相互作用的丧失大大降低了 eIF4E 与 TOP 和 TOP 样 mRNAs 结合的能力,比其他 mRNAs 多得多,这解释了为什么 mTOR 抑制选择性抑制它们的翻译。我们的结果阐明了 mTORC1 控制的翻译程序,并确定 4E-BPs 和 eIF4G1 是其主要效应物。