The Importance of the Helix 2 Region for the cis-Cleaving and trans-Cleaving Activities of Hepatitis Delta Virus Ribozymes

• Published in: Biochemistry (Easton) 1996-09, Vol.35 (38), p.12303-12312
• Main Authors: Lee, Chuan-Bin, Lai, Yen-Chein, Ping, Yueh-Hsin, Huang, Zhi-Shun, Lin, Jung-Yaw, Wu, Huey-Nan
• Format: Article
• Language: English
• Subjects: Base Sequence; Electrophoresis, Polyacrylamide Gel; Formamides - pharmacology; Hepatitis Delta Virus - chemistry; Kinetics; Molecular Sequence Data; Mutagenesis; Nucleic Acid Conformation; Nucleic Acid Denaturation; Polymerase Chain Reaction; Ribonucleases - metabolism; RNA, Catalytic - chemistry; RNA, Catalytic - metabolism
• ISSN: 0006-2960; 1520-4995
• DOI: 10.1021/bi961219m

The sequence, secondary structure, and size requirements of the helix 2 region (H2) of a cis-acting hepatitis delta virus ribozyme Rz 1 were examined in this study. Mutational analysis was performed, and the cleavage rate of each H2 mutant of Rz 1 was assayed. We found that H2 could be elongated to twice its original size without affecting ribozyme folding while the shortening of H2 by one base pair severely decreased autolytic activity. In addition, the maintenance of the Watson−Crick base-pairing interactions of the last base pair of H2 (A16U58) was not critical for cis-cleavage reaction. Nevertheless, mutants with an AA, an AG, an AC, or a GG pair at the bottom of H2 were less active, and the sequence of the H2/H3 interface might affect the stability of the catalytic core. The negative effects on ribozyme folding, such as the destabilization of H2, the unfavorable sequences at the last base pair of H2 as well as the disruption of the continuity of H2 and H3, could be compensated for by elongating the H2 region of the corresponding mutants. The extension of H2 may alter the conformation of ribozyme molecules; in addition, it stabilized the catalytic core and enhanced the resistance to formamide. Finally, for a trans-acting ribozyme and its substrate that require the formation of H1, H2, and H4 to reconstitute the autocatalytic domain of HDV RNA, the extension of H2 stabilized the substrate/ribozyme complex and speeded up the cleavage rate but hindered the product release process.