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      Close packing of helices 3 and 12 of 16 S rRNA is required for the normal ribosome function.

      The Journal of Biological Chemistry
      Amino Acid Motifs, Computer Simulation, Escherichia coli, metabolism, Gene Library, Green Fluorescent Proteins, Hydrogen Bonding, Models, Chemical, Models, Molecular, Nucleic Acid Conformation, Plasmids, Protein Binding, RNA, Ribosomal, chemistry, RNA, Ribosomal, 16S, Ribosomes, Uridine

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          Abstract

          The along-groove packing motif is a quasi-reciprocal arrangement of two RNA double helices in which a backbone of each helix is closely packed within the minor groove of the other helix. At the center of the inter-helix contact, a GU base pair in one helix packs against a Watson-Crick base pair in the other helix. Here, based on in vivo selection from a combinatorial gene library of 16 S rRNA and on functional characterization of the selected clones, we demonstrate that the normal ribosome performance requires that helices 3 and 12 be closely packed. In some clones the Watson-Crick and GU base pairs exchange in their positions between the two helices, which affects neither the quality of the helix packing, nor the ribosome function. On the other hand, perturbations in the close packing usually lead to a substantial drop in the ribosome activity. The functionality of the clones containing such perturbations may depend on the presence of particular elements in the vicinity of the area of contact between helices 3 and 12. Such cases do not exist in natural 16 S rRNA, and their selection enriches our knowledge of the constraints imposed on the structure of ribosomal RNA in functional ribosomes.

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