Département de microbiologie et d'infectiologie, Faculté de médecine et des sciences de la santé, Université de Sherbrooke, Sherbrooke, QC J1E 4K8 Canada.
Commun Biol. 2019 Jun 17;2:211. doi: 10.1038/s42003-019-0441-3. eCollection 2019.
Cell cycle progression depends on phase-specific gene expression. Here we show that the nuclear RNA degradation machinery plays a lead role in promoting cell cycle-dependent gene expression by triggering promoter-dependent co-transcriptional RNA degradation. Single molecule quantification of RNA abundance in different phases of the cell cycle indicates that relative curtailment of gene expression in certain phases is attained even when transcription is not completely inhibited. When nuclear ribonucleases are deleted, transcription of the G1-specific axial budding gene is detected throughout the cell cycle and its phase-specific expression is lost. Promoter replacement abolished cell cycle-dependent RNA degradation and rendered the RNA insensitive to the deletion of nuclear ribonucleases. Together the data reveal a model of gene regulation whereby RNA abundance is controlled by promoter-dependent induction of RNA degradation.
细胞周期的进展依赖于特定相位的基因表达。在这里,我们表明核 RNA 降解机制通过触发启动子依赖性共转录 RNA 降解,在促进细胞周期依赖性基因表达方面发挥主导作用。在细胞周期的不同相位中对 RNA 丰度进行单分子定量表明,即使转录不完全被抑制,在某些相位中基因表达的相对缩短也能实现。当核核糖核酸酶被删除时,G1 特异性轴向出芽基因的转录在整个细胞周期中被检测到,其特定相位的表达丧失。启动子替换消除了细胞周期依赖性 RNA 降解,并使 RNA 对核核糖核酸酶的缺失不敏感。这些数据共同揭示了一种基因调控模型,其中 RNA 的丰度通过启动子依赖性诱导 RNA 降解来控制。