Sivan Gilad, Elroy-Stein Orna
Department of Cell Research & Immunology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.
Cell Cycle. 2008 Mar 15;7(6):741-4. doi: 10.4161/cc.7.6.5596. Epub 2008 Jan 8.
Protein synthesis is a multistep, multifactorial process of mRNA translation, on which cells expend more energy than on any other activity. Cellular division into two daughter cells involves temporary inhibition of protein synthesis. In line with many translational control paradigms, global translation during mitosis is inhibited at the level of 5'cap-dependent initiation. The down regulation of global translation is accompanied by 5'cap-independent translational activation of specific mRNAs whose protein products have a role in the progression of cellular division. Recently, the elongation step was highlighted as a major target of translational control during mitosis, in addition to the initiation step. Stalling of translating ribosomes not only protects mRNAs during mitosis but also allows rapid resumption of active translation immediately upon entry into the G(1) phase of the cell cycle, an added dimension of energy saving. This review focuses on recent information related to translational regulation during cellular division and raises a new challenge regarding mechanism(s) employed by mRNAs whose translation is not sensitive to the elongation block.
蛋白质合成是一个多步骤、多因素的mRNA翻译过程,细胞在这一过程中消耗的能量比其他任何活动都多。细胞分裂为两个子细胞涉及蛋白质合成的暂时抑制。与许多翻译控制模式一致,有丝分裂期间的整体翻译在5'帽依赖性起始水平受到抑制。整体翻译的下调伴随着特定mRNA的5'帽非依赖性翻译激活,其蛋白质产物在细胞分裂进程中发挥作用。最近,除了起始步骤外,延伸步骤被强调为有丝分裂期间翻译控制的主要靶点。翻译核糖体的停滞不仅在有丝分裂期间保护mRNA,还能在进入细胞周期的G(1)期后立即迅速恢复活跃翻译,这是节能的一个新方面。本综述重点关注细胞分裂期间与翻译调控相关的最新信息,并对翻译对延伸阻滞不敏感的mRNA所采用的机制提出了新的挑战。