Structural Simplicity and Mechanistic Complexity in the Hammerhead Ribozyme

Prog Mol Biol Transl Sci. 2018:159:177-202. doi: 10.1016/bs.pmbts.2018.07.006. Epub 2018 Sep 17.

Abstract

Natural or full-length hammerhead ribozymes are up to 1000-fold more active than their minimal counterparts that lack a complex tertiary interaction that pre-organizes and stabilizes the ribozyme active site, positioning RNA functional groups to facilitate acid-base catalysis. The recent discovery that a single tertiary contact (an AU Hoogsteen pair) between Stems I and II confers essentially all of the enhanced activity greatly simplifies our understanding of the structural requirements for hammerhead ribozyme activity. In contrast, the simplest mechanistic interpretations are challenged with the presentation of more complex alternatives. These alternatives are elucidated and critically analyzed in the context of several of the active hammerhead ribozyme structures now available.

Keywords: Acid-base catalysis; Fast minimal hammerhead; Hammerhead ribozyme catalysis; Hammerhead ribozyme structure; Tertiary contact.

Publication types

  • Review

MeSH terms

  • Animals
  • Base Sequence
  • Catalysis
  • Catalytic Domain
  • Humans
  • Hydrogen-Ion Concentration
  • Nucleic Acid Conformation
  • RNA, Catalytic / chemistry*
  • RNA, Catalytic / metabolism*

Substances

  • RNA, Catalytic
  • hammerhead ribozyme