The Menu of Features that Define Primary MicroRNAs and Enable De Novo Design of MicroRNA Genes

Mol Cell. 2015 Oct 1;60(1):131-45. doi: 10.1016/j.molcel.2015.08.015. Epub 2015 Sep 24.

Abstract

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.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Computational Biology / methods*
  • DEAD-box RNA Helicases / metabolism
  • HEK293 Cells
  • Humans
  • MicroRNAs / metabolism*
  • Models, Molecular
  • Nucleic Acid Conformation
  • RNA Precursors / chemistry*
  • RNA Precursors / metabolism
  • RNA Processing, Post-Transcriptional
  • Ribonuclease III / metabolism

Substances

  • MicroRNAs
  • RNA Precursors
  • DICER1 protein, human
  • DROSHA protein, human
  • Ribonuclease III
  • DEAD-box RNA Helicases

Associated data

  • GEO/GSE67937