Singapore-MIT Alliance for Research and Technology, 1 CREATE Way, 138602, Singapore.
Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, 02139, USA.
Genome Biol. 2018 Dec 27;19(1):228. doi: 10.1186/s13059-018-1611-1.
Cells adapt to stress by altering gene expression at multiple levels. Here, we propose a new mechanism regulating stress-dependent gene expression at the level of translation, with coordinated interplay between the tRNA epitranscriptome and biased codon usage in families of stress-response genes. In this model, auxiliary genetic information contained in synonymous codon usage enables regulation of codon-biased and functionally related transcripts by dynamic changes in the tRNA epitranscriptome. This model partly explains the association between synchronous stress-dependent epitranscriptomic marks and significant multi-codon usage skewing in families of translationally regulated transcripts. The model also predicts translational adaptation during viral infections.
细胞通过在多个层面改变基因表达来适应应激。在这里,我们提出了一种新的机制,即在翻译水平上调节应激相关基因表达,在应激反应基因家族中,tRNA 表转录组和偏向密码子使用之间进行协调相互作用。在这个模型中,同义密码子使用中包含的辅助遗传信息使通过 tRNA 表转录组的动态变化来调节密码子偏向和功能相关的转录本成为可能。该模型部分解释了同步应激依赖的表转录组标记与翻译调控转录本家族中显著的多密码子使用倾斜之间的关联。该模型还预测了病毒感染期间的翻译适应性。