Tahmasebi Soroush, Amiri Mehdi, Sonenberg Nahum
Department of Pharmacology, University of Illinois at Chicago, Chicago, IL, United States.
Goodman Cancer Research Center, McGill University, Montreal, QC, Canada.
Front Genet. 2019 Jan 15;9:709. doi: 10.3389/fgene.2018.00709. eCollection 2018.
Simultaneous measurements of mRNA and protein abundance and turnover in mammalian cells, have revealed that a significant portion of the cellular proteome is controlled by mRNA translation. Recent studies have demonstrated that both embryonic and somatic stem cells are dependent on low translation rates to maintain an undifferentiated state. Conversely, differentiation requires increased protein synthesis and failure to do so prevents differentiation. Notably, the low translation in stem cell populations is independent of the cell cycle, indicating that stem cells use unique strategies to decouple these fundamental cellular processes. In this chapter, we discuss different mechanisms used by stem cells to control translation, as well as the developmental consequences of translational deregulation.
对哺乳动物细胞中mRNA丰度、蛋白质丰度及周转率的同步测量表明,细胞蛋白质组的很大一部分受mRNA翻译的控制。最近的研究表明,胚胎干细胞和体细胞干细胞都依赖低翻译速率来维持未分化状态。相反,分化需要增加蛋白质合成,而未能如此则会阻止分化。值得注意的是,干细胞群体中的低翻译与细胞周期无关,这表明干细胞使用独特的策略来使这些基本细胞过程脱钩。在本章中,我们将讨论干细胞用于控制翻译的不同机制,以及翻译失调的发育后果。