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. 2001 Jan 2;98(1):130–135. doi: 10.1073/pnas.98.1.130

Figure 1.

Figure 1

The hairpin ribozyme library and gene vector. (A) Sequence and secondary structure of the hairpin ribozyme (capital letters), bound to its target RNA (lowercase letters). Both target-binding arms (helices 1 & 2) are randomized, generating a library with as many as 412 different catalytic molecules (ribozymes). (B) Schematic representation of the retroviral vector following insertion of the ribozyme library DNA template. Ribozyme expression is driven by the tRNAval promoter. (C) Flow cytometry for EGFP of SK-BR-3, PA-1, and T47-D cells. Numbers in parentheses indicate the relative expression levels of endogenous BRCA1. Analysis of untransfected control cells (parental cells) and dilution clones from cells, transfected with pBR-EGFP (BR-EGFP) or with pCMV-EGFP (CMV-EGFP).