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Contact: Alistair R. R. Forrest
public@gsc.riken.jp
81-455-039-222
RIKEN

HeliScopeCAGE Protocol Workflow

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

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Related news release: HeliScopeCAGE: A new gene expression analysis technique on a single molecule sequencer


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