Young David J, Wang Yuejun, Guydosh Nicholas R
Laboratory of Biochemistry and Genetics, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health Bethesda, MD 20892 USA.
TriLab Bioinformatics Group, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health Bethesda, MD 20892 USA.
bioRxiv. 2025 Aug 17:2025.08.15.670413. doi: 10.1101/2025.08.15.670413.
The nonsense-mediated mRNA decay (NMD) pathway targets mRNAs undergoing premature translation termination for degradation. Previously, RNA-seq of yeast lacking NMD revealed that most genes targeted by NMD lack obvious premature termination codons (PTCs). We developed a combined approach using RNA-seq and a novel 40S ribosome profiling strategy to identify cryptic premature termination events that could account for NMD on nearly all these transcripts, including many non-coding RNA transcript isoforms associated with annotated genes. Many NMD-targeted transcripts appear to be involved in two-promoter gene regulatory systems and share properties with long un-decoded transcript isoforms (LUTIs). In particular, we show that the LUTI regulates expression of the protein-coding mRNA in response to changes to environmental nitrogen. Our work expands the functional roles for LUTIs and establishes the importance of NMD in their regulation.
无义介导的mRNA降解(NMD)途径会将经历过早翻译终止的mRNA靶向降解。此前,对缺乏NMD的酵母进行RNA测序发现,NMD靶向的大多数基因缺乏明显的过早终止密码子(PTC)。我们开发了一种结合RNA测序和新型40S核糖体分析策略的方法,以识别潜在的过早终止事件,这些事件可能解释了几乎所有这些转录本上的NMD现象,包括许多与注释基因相关的非编码RNA转录本异构体。许多NMD靶向的转录本似乎参与了双启动子基因调控系统,并与长未解码转录本异构体(LUTI)具有共同特性。特别是,我们表明LUTI会响应环境氮的变化来调节蛋白质编码mRNA的表达。我们的工作扩展了LUTI的功能作用,并确立了NMD在其调控中的重要性。