Science for Life Laboratory, Department of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, Stockholm, Sweden.
Science for Life Laboratory, Department of Molecular Biosciences, The Wenner-Gren Institute, Stockholm University, Stockholm, Sweden; The Arctic University Museum of Norway, UiT - The Arctic University of Norway, Tromsø, Norway.
Cell Rep. 2021 Nov 16;37(7):110015. doi: 10.1016/j.celrep.2021.110015.
Previous large-scale studies have uncovered many features that determine the processing of microRNA (miRNA) precursors; however, they have been conducted in vitro. Here, we introduce MapToCleave, a method to simultaneously profile processing of thousands of distinct RNA structures in living cells. We find that miRNA precursors with a stable lower basal stem are more efficiently processed and also have higher expression in vivo in tissues from 20 animal species. We systematically compare the importance of known and novel sequence and structural features and test biogenesis of miRNA precursors from 10 animal and plant species in human cells. Lastly, we provide evidence that the GHG motif better predicts processing when defined as a structure rather than sequence motif, consistent with recent cryogenic electron microscopy (cryo-EM) studies. In summary, we apply a screening assay in living cells to reveal the importance of lower basal stem stability for miRNA processing and in vivo expression.
先前的大规模研究已经揭示了许多决定 microRNA (miRNA) 前体加工的特征;然而,这些研究都是在体外进行的。在这里,我们引入了 MapToCleave 方法,这是一种可以同时在活细胞中对数千种不同 RNA 结构的加工进行分析的方法。我们发现,具有稳定较低基础茎的 miRNA 前体在 20 种动物组织中的加工效率更高,体内表达水平也更高。我们系统地比较了已知和新的序列和结构特征的重要性,并在人细胞中测试了来自 10 种动物和植物物种的 miRNA 前体的生物发生。最后,我们提供了证据表明,当 GHG 基序被定义为结构而不是序列基序时,它可以更好地预测加工,这与最近的低温电子显微镜 (cryo-EM) 研究一致。总之,我们在活细胞中应用筛选分析来揭示较低基础茎稳定性对 miRNA 加工和体内表达的重要性。