HeliScopeCAGE Protocol Workflow (image) RIKEN Share Print E-Mail Caption (A) Reverse transcription. cDNA is synthesized using SuperScript III and random N15 primer. (B) Oxidation/Biotinylation. The cap structure is oxidized with sodium peroxide and biotinylated with biotin (long arm) hydrazine. (C) RNase I digestion. Single strand RNA is digested with RNase I. (D) Capture on magnetic streptavidin beads. Biotinylated RNA/cDNA hybrid molecules are captured using magnetic streptavidin beads. (E) Wash unbound molecules. Unbound RNA/DNA hybrid molecules are washed away. (F) Release ss-cDNA. Captured RNA/DNA hybrid molecules are treated with RNase H and RNase I, then heat treated. (G) Poly-A tailing/blocking. Released cDNA is poly-A tailed using terminal deoxynucleotidyl transferase and dATP, then blocked with biotin-ddATP. (H) Load on flow cell. Blocked poly-A tailed cDNA is loaded on the HeliScope flow cell channel and anneals with the dT 50 surface. (I) Fill with dTTP/locked with A/G/C virtual terminator. After annealing of cDNA, the single strand poly-A tail part is filled with DNA polymerase, dTTP, and an A/G/C virtual terminator which is used for the HeliScope sequencing to lock the poly-T termini. The library is then ready for sequencing. Credit RIKEN Usage Restrictions None Share Print E-Mail Disclaimer: AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert system.