Department of Hematology, Inselspital, Bern University Hospital, University of Bern, CH-3008 Bern, Switzerland.
Department of BioMedical Research, University of Bern, CH-3008 Bern, Switzerland.
Int J Mol Sci. 2021 Jan 28;22(3):1287. doi: 10.3390/ijms22031287.
Protein synthesis is a highly complex process executed by well-organized translation machinery. Ribosomes, tRNAs and mRNAs are the principal components of this machinery whereas RNA binding proteins and ribosome interacting partners act as accessory factors. Angiogenin (ANG)-Ribonuclease inhibitor (RNH1) system is one such accessory part of the translation machinery that came into focus afresh due to its unconventional role in the translation. ANG is conventionally known for its ability to induce blood vessel formation and RNH1 as a "sentry" to protect RNAs from extracellular RNases. However, recent studies suggest them to be important in translation regulation. During cell homeostasis, ANG in the nucleus promotes rRNA transcription. While under stress, ANG translocates to the cytosol and cleaves tRNA into fragments which inhibit ribosome biogenesis and protein synthesis. RNH1, which intimately interacts with ANG to inhibit its ribonucleolytic activity, can also bind to the 40S ribosomes and control translation by yet to be known mechanisms. Here, we review recent advancement in the knowledge of translation regulation by the ANG-RNH1 system. We also gather information about this system in cell homeostasis as well as in pathological conditions such as cancer and ribosomopathies. Additionally, we discuss the future research directions and therapeutic potential of this system.
蛋白质合成是一个由高度组织化的翻译机制执行的高度复杂过程。核糖体、tRNA 和 mRNA 是该机制的主要成分,而 RNA 结合蛋白和核糖体相互作用伙伴则作为辅助因子发挥作用。血管生成素 (ANG)-核糖核酸酶抑制剂 (RNH1) 系统是翻译机制的一个辅助部分,由于其在翻译中的非常规作用,该系统重新成为焦点。ANG 通常因其诱导血管形成的能力而闻名,而 RNH1 则作为“哨兵”,保护 RNA 免受细胞外核糖核酸酶的侵害。然而,最近的研究表明它们在翻译调控中很重要。在细胞内稳态期间,核内的 ANG 促进 rRNA 转录。而在应激下,ANG 易位到细胞质中并将 tRNA 切割成片段,从而抑制核糖体生物发生和蛋白质合成。与 ANG 密切相互作用以抑制其核糖核酸酶活性的 RNH1,也可以与 40S 核糖体结合,并通过尚未明确的机制控制翻译。在这里,我们回顾了 ANG-RNH1 系统在翻译调控方面的最新进展。我们还收集了关于该系统在细胞内稳态以及癌症和核糖体病等病理条件下的信息。此外,我们还讨论了该系统的未来研究方向和治疗潜力。