Fang Wenwen, Bartel David P
Howard Hughes Medical Institute, Cambridge, MA 02142, USA; Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Howard Hughes Medical Institute, Cambridge, MA 02142, USA; Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Mol Cell. 2015 Oct 1;60(1):131-45. doi: 10.1016/j.molcel.2015.08.015. Epub 2015 Sep 24.
MicroRNAs (miRNAs) are small regulatory RNAs processed from stem-loop regions of primary transcripts (pri-miRNAs), with the choice of stem loops for initial processing largely determining what becomes a miRNA. To identify sequence and structural features influencing this choice, we determined cleavage efficiencies of >50,000 variants of three human pri-miRNAs, focusing on the regions intractable to previous high-throughput analyses. Our analyses revealed a mismatched motif in the basal stem region, a preference for maintaining or improving base pairing throughout the remainder of the stem, and a narrow stem-length preference of 35 ± 1 base pairs. Incorporating these features with previously identified features, including three primary-sequence motifs, yielded a unifying model defining mammalian pri-miRNAs in which motifs help orient processing and increase efficiency, with the presence of more motifs compensating for structural defects. This model enables generation of artificial pri-miRNAs, designed de novo, without reference to any natural sequence yet processed more efficiently than natural pri-miRNAs.
微小RNA(miRNA)是从初级转录本(pri-miRNA)的茎环区域加工而来的小调节RNA,茎环的初始加工选择在很大程度上决定了哪些会成为miRNA。为了确定影响这种选择的序列和结构特征,我们测定了三种人类pri-miRNA的50000多个变体的切割效率,重点关注先前高通量分析难以处理的区域。我们的分析揭示了基部茎区域中的错配基序,在茎的其余部分保持或改善碱基配对的偏好,以及35±1个碱基对的狭窄茎长偏好。将这些特征与先前确定的特征(包括三个一级序列基序)相结合,产生了一个定义哺乳动物pri-miRNA的统一模型,其中基序有助于定向加工并提高效率,更多基序的存在可补偿结构缺陷。该模型能够从头设计生成人工pri-miRNA,无需参考任何天然序列,但其加工效率却高于天然pri-miRNA。