Self-Assembly of a Group I Intron from Inactive Oligonucleotide Fragments

Eric J. Hayden, Niles Lehman

Research output: Contribution to journalArticlepeer-review

86 Scopus citations

Abstract

The Azoarcus group I ribozyme was broken into four fragments, 39-63 nucleotides long, that can self-assemble into covalently contiguous ribozymes via RNA-directed recombination events. The fragments have no activity individually yet can cooperate through base pairing and tertiary interactions to produce stable trans complexes at 48°C. These complexes can then catalyze a sequence of energy-neutral recombination reactions utilizing other oligomers as substrates, assembling covalent versions of the ribozyme. Up to 17% of the original fragments are converted into ∼200 nucleotide products in 8 hr. Assembly occurs primarily by only one of many possible pathways, and the reaction is driven in the correct and forward direction by the burial of key base-pairing regions in stems after recombination. Autocatalysis, and hence self-replication, is inferred by a reaction rate increase upon doping the reaction with full-length RNA.

Original languageEnglish
Pages (from-to)909-918
Number of pages10
JournalChemistry and Biology
Volume13
Issue number8
DOIs
StatePublished - Aug 2006

Keywords

  • Azoarcus/enzymology
  • Base Sequence
  • Catalysis
  • Introns
  • Molecular Sequence Data
  • Oligonucleotides/chemistry
  • RNA/chemistry
  • RNA, Catalytic/chemistry
  • Recombination, Genetic
  • Substrate Specificity

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