Cao Dan, Parker Roy
Department of Molecular and Cellular Biology and Howard Hughes Medical Institute, University of Arizona, Tucson, AZ 85721, USA.
Cell. 2003 May 16;113(4):533-45. doi: 10.1016/s0092-8674(03)00353-2.
A conserved mRNA surveillance system, referred to as nonsense-mediated decay (NMD), exists in eukaryotic cells to degrade mRNAs containing nonsense codons. This process is important in checking that mRNAs have been properly synthesized and functions, at least in part, to increase the fidelity of gene expression by degrading aberrant mRNAs that, if translated, would produce truncated proteins. Using computational modeling and experimental analysis, we define the alterations in mRNA turnover triggered by NMD in yeast. We demonstrate that the nonsense-containing transcripts are efficiently recognized, targeted for deadenylation-independent decapping, and show NMD triggered accelerated deadenylation regardless of the position of the nonsense codon. We also show that 5' nonsense codons trigger faster rates of decapping than 3' nonsense codons, thereby providing a mechanistic basis for the polar effect of NMD. Finally, we construct a computational model that accurately describes the process of NMD and serves as an explanatory and predictive tool.
一种保守的mRNA监测系统,即无义介导的衰变(NMD),存在于真核细胞中,用于降解含有无义密码子的mRNA。这一过程对于检查mRNA是否已正确合成并发挥功能很重要,并且至少部分地通过降解异常mRNA来提高基因表达的保真度,这些异常mRNA如果被翻译,会产生截短的蛋白质。通过计算建模和实验分析,我们定义了酵母中由NMD触发的mRNA周转变化。我们证明,含无义密码子的转录本能被有效识别,靶向不依赖于去腺苷酸化的脱帽过程,并且无论无义密码子的位置如何,NMD都会触发加速的去腺苷酸化。我们还表明,5'端无义密码子比3'端无义密码子触发更快的脱帽速率,从而为NMD的极性效应提供了一个机制基础。最后,我们构建了一个计算模型,该模型准确地描述了NMD的过程,并作为一个解释性和预测性工具。