In vivo selection of GFP-expressing replicons. (A) Organization of pF1fsdsGFP and derivatives containing variations in part of the DSCE and/or PSCE, illustrated as in Fig. 3A. In accordance with standard International Union of Pure and Applied Chemistry nomenclature, N = any nucleoside; V = A, C, or G; H = A, C, or U; D = A, G, or U; and B = C, G, or U. (B) Cell fluorescence versus forward scattering (FSC), as plotted for 104 cells of the indicated cultures. The gates used for cell sorting and percentages of the total within these bounds are shown. (C) Northern blots of RNAs extracted from the indicated bulk cultures were probed for RNA1 and RNA3 positive strands as indicated in Fig. 1B. (D) MscI digestion of pF1fsdsGFP or the indicated pF1fsdsGFPran1 plasmid pools: library, original plasmid library prior to yeast transformation; unsorted, plasmids after recovery from an unsorted yeast population; sorted, plasmids after recovery from a yeast population sorted as for panel B. M, DNA size standards, HindIII-cut bacteriophage λ genome, and 100-bp ladder (New England Biolabs).