miR-ID: A novel, circularization-based platform for detection of microRNAs

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FIGURE 3.
FIGURE 3.

Circularization of miRNAs having a 2′-oxymethyl modification at their 3′-ends (2′-OMe miRNAs). (A) Using T4 RNA ligase 1 (Rnl1) at 37°C. (B) Using CircLigase II (CLII) at 60°C. 80 nM synthetic miRNAs (let-7b, let-7g, miR-16, and miR-23a), which have four different nucleotides with 2′-OMe and 3′-OH at their 3′-termini, were 32P-labeled at their 5′-ends and then circularized using either ligase. Aliquots were taken at 0, 1, 15, and 60 min during the courses of the ligation reactions and analyzed on a denaturing 15% polyacrylamide gel. The reaction products include the unmodified linear, 5′-adenylated linear, and circular forms of the miRNAs as shown.

This Article

  1. RNA 17: 365-380