High-efficiency RNA cloning enables accurate quantification of miRNA expression by deep sequencing

Genome Biol. 2013;14(10):R109. doi: 10.1186/gb-2013-14-10-r109.

Abstract

Small RNA cloning and sequencing is uniquely positioned as a genome-wide approach to quantify miRNAs with single-nucleotide resolution. However, significant biases introduced by RNA ligation in current protocols lead to inaccurate miRNA quantification by 1000-fold. Here we report an RNA cloning method that achieves over 95% efficiency for both 5′ and 3′ ligations. It achieves accurate quantification of synthetic miRNAs with less than two-fold deviation from the anticipated value and over a dynamic range of four orders of magnitude. Taken together, this high-efficiency RNA cloning method permits accurate genome-wide miRNA profiling from total RNAs.

Publication types

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

MeSH terms

  • Cloning, Molecular*
  • Down-Regulation
  • Gene Expression Regulation
  • Gene Expression*
  • High-Throughput Nucleotide Sequencing* / methods
  • High-Throughput Nucleotide Sequencing* / standards
  • MicroRNAs / chemistry
  • MicroRNAs / genetics*
  • RNA Folding
  • RNA Interference

Substances

  • MicroRNAs

Associated data

  • GEO/GSE47858