Detailed analysis of stem I and its 5 ' and 3 ' neighbor regions in the trans-acting HDV ribozyme

To determine the stem I structure of the human hepatitis delta virus (HDV) ribozyme, which is related to the substrate sequence in the trans-acting sy stem, we kinetically studied stem I length and sequences. Stem I extension from 7 to 8 or 9 bp caused a loss of activity and a low amount of active co mplex with 9 bp in the trans-acting system. In a previous report, we presen ted cleavage in a 6 bp stem I. The observed reaction rates indicate that th e original 7 bp stem I is in the most favorable location for catalytic reac tion among the possible 6-8 bp stems. To test base specificity, we replaced the original CC-rich sequence in stem I with AU-rich sequences containing six AU or UA base pairs with the natural +1G.U wobble base pair at the clea vage site. The cis-acting AU-rich molecules demonstrated similar catalytic activity to that of the wild-type. In trans-acting molecules, due to stem I instability, reaction efficiency strongly depended on the concentration of the ribozyme-substrate complex and reaction temperature. Multiple turnover was observed at 37 degrees C, strongly suggesting that stem I has no base specificity and more efficient activity can be expected under multiple turn over conditions by substituting several UA or AU base pairs into stem I, We also studied the substrate damaging sequences linked to both ends of stem I for its development in therapeutic applications and confirmed the functio ns of the unique structure.