Department of Molecular, Cell and Developmental Biology, University of California, Santa Cruz, Santa Cruz, United States.
Departments of Pathology and Genetics, Stanford University School of Medicine, Stanford, United States.
Elife. 2018 Jan 8;7:e33292. doi: 10.7554/eLife.33292.
Nonsense-mediated mRNA decay is the process by which mRNAs bearing premature stop codons are recognized and cleared from the cell. While considerable information has accumulated regarding recognition of the premature stop codon, less is known about the ensuing mRNA suppression. During the characterization of a second, distinct translational surveillance pathway (nonstop mRNA decay), we trapped intermediates in nonsense mRNA degradation. We present data in support of a model wherein nonsense-mediated decay funnels into the nonstop decay pathway in . Specifically, our results point to SKI-exosome decay and pelota-based ribosome removal as key steps facilitating suppression and clearance of prematurely-terminated translation complexes. These results suggest a model in which premature stop codons elicit nucleolytic cleavage, with the nonstop pathway disengaging ribosomes and degrading the resultant RNA fragments to suppress ongoing expression.
无意义介导的 mRNA 衰减是一种识别并清除带有过早终止密码子的 mRNA 的过程。虽然已经积累了大量关于识别过早终止密码子的信息,但对于随后的 mRNA 抑制知之甚少。在对第二个不同的翻译监控途径(非终止 mRNA 衰减)进行特征描述时,我们捕获了无意义 mRNA 降解过程中的中间体。我们提供的数据支持了这样一种模型,即无意义介导的降解在. 中汇入非终止衰变途径。具体来说,我们的结果表明 SKI-外切体降解和基于 pelota 的核糖体去除是促进过早终止翻译复合物抑制和清除的关键步骤。这些结果表明,一种模型可以解释过早终止密码子引发核酶切割,而非终止途径脱离核糖体并降解产生的 RNA 片段以抑制正在进行的表达。