Alalam Hanna, Šafhauzer Monika, Sunnerhagen Per
Department of Chemistry and Molecular Biology, University of Gothenburg, 413 90 Göteborg, Sweden.
Department of Chemistry and Molecular Biology, University of Gothenburg, 413 90 Göteborg, Sweden
RNA. 2025 Mar 18;31(4):600-611. doi: 10.1261/rna.080272.124.
Nonsense-mediated decay (NMD) is a eukaryotic surveillance pathway that controls degradation of cytoplasmic transcripts with aberrant features. NMD-controlled RNA degradation acts to regulate a large fraction of the mRNA population. It has been implicated in cellular responses to infections and environmental stress, as well as in deregulation of tumor-promoting genes. NMD is executed by a set of three core factors conserved in evolution, UPF1-3, as well as additional influencing proteins such as kinases. Monitoring NMD activity is challenging due to the difficulties in quantitating RNA decay rates in vivo, and consequently, it has also been problematic to identify new factors influencing NMD. Here, we developed a genetic selection system in yeast to capture new components affecting NMD status. The reporter constructs link NMD target sequences with nutrient-selectable genetic markers. By crossing these reporters into a genome-wide library of deletion mutants and quantitating colony growth on a selective medium, we robustly detect previously known NMD components in a high-throughput fashion. In addition, we identify novel mutations influencing NMD status and implicate ribosome recycling as important for NMD. By using our constructed combinations of promoters, NMD target sequences, and selectable markers, the system can also efficiently detect mutations with a minor effect, or in special environments. Furthermore, it can be used to explore how NMD acts on targets of different structures.
无义介导的衰变(NMD)是一种真核生物监测途径,可控制具有异常特征的细胞质转录本的降解。NMD控制的RNA降解作用于调节大部分mRNA群体。它与细胞对感染和环境应激的反应有关,也与肿瘤促进基因的失调有关。NMD由一组在进化中保守的三个核心因子UPF1 - 3以及其他影响蛋白(如激酶)执行。由于在体内定量RNA衰变率存在困难,监测NMD活性具有挑战性,因此,识别影响NMD的新因子也存在问题。在这里,我们在酵母中开发了一种遗传筛选系统,以捕获影响NMD状态的新成分。报告构建体将NMD靶序列与营养选择型遗传标记连接起来。通过将这些报告基因与全基因组缺失突变体文库杂交,并在选择培养基上定量菌落生长,我们以高通量方式可靠地检测到先前已知的NMD成分。此外,我们鉴定了影响NMD状态的新突变,并表明核糖体循环对NMD很重要。通过使用我们构建的启动子、NMD靶序列和选择标记的组合,该系统还可以有效地检测具有微小影响的突变,或在特殊环境中的突变。此外,它可用于探索NMD如何作用于不同结构的靶标。