Giess Adam, Torres Cleuren Yamila N, Tjeldnes Håkon, Krause Maximilian, Bizuayehu Teshome Tilahun, Hiensch Senna, Okon Aniekan, Wagner Carston R, Valen Eivind
Computational Biology Unit, Department of Informatics, University of Bergen, Bergen 5020, Norway.
Computational Biology Unit, Department of Informatics, University of Bergen, Bergen 5020, Norway.
Cell Rep. 2020 Apr 21;31(3):107534. doi: 10.1016/j.celrep.2020.107534.
Translation initiation is often attributed as the rate-determining step of eukaryotic protein synthesis and key to gene expression control. Despite this centrality, the series of steps involved in this process is poorly understood. Here, we capture the transcriptome-wide occupancy of ribosomes across all stages of translation initiation, enabling us to characterize the transcriptome-wide dynamics of ribosome recruitment to mRNAs, scanning across 5' UTRs and stop codon recognition, in a higher eukaryote. We provide mechanistic evidence for ribosomes attaching to the mRNA by threading the mRNA through the small subunit. Moreover, we identify features that regulate the recruitment and processivity of scanning ribosomes and redefine optimal initiation contexts. Our approach enables deconvoluting translation initiation into separate stages and identifying regulators at each step.
翻译起始通常被认为是真核生物蛋白质合成的限速步骤以及基因表达控制的关键。尽管其处于核心地位,但该过程中涉及的一系列步骤却鲜为人知。在此,我们捕获了翻译起始所有阶段核糖体在全转录组范围内的占据情况,从而能够在高等真核生物中描绘核糖体募集到mRNA、扫描5'非翻译区以及识别终止密码子的全转录组动力学。我们提供了核糖体通过将mRNA穿过小亚基而附着到mRNA上的机制证据。此外,我们鉴定了调节扫描核糖体募集和持续性的特征,并重新定义了最佳起始上下文。我们的方法能够将翻译起始解卷积为不同阶段,并识别每个步骤的调节因子。