Structural requirement for Mg2+ binding in the group I intron core

J Mol Biol. 2003 May 30;329(2):229-38. doi: 10.1016/s0022-2836(03)00430-3.

Abstract

Divalent metal ions are required for splicing of group I introns, but their role in maintaining the structure of the active site is still under investigation. Ribonuclease and hydroxyl radical footprinting of a small group I intron from Azoarcus pre-tRNA(Ile) showed that tertiary interactions between helical domains are stable in a variety of cations. Only Mg(2+), however, induced a conformational change in the intron core that correlates with self-splicing activity. Three metal ion binding sites in the catalytic core were identified by Tb(III)-dependent cleavage. Two of these are near bound substrates in a three-dimensional model of the ribozyme. A third metal ion site is near an A minor motif in P3. In the pre-tRNA, Tb(3+) cleavage was redirected to the 5' and 3' splice sites, consistent with metal-dependent activation of splice site phosphodiesters. The results show that many counterions induce global folding, but organization of the group I active site is specifically linked to Mg(2+) binding at a few sites.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Azoarcus / genetics
  • Base Sequence
  • Binding Sites
  • Catalysis
  • Conserved Sequence / genetics
  • Exons / genetics
  • Introns / physiology*
  • Magnesium / metabolism*
  • Molecular Sequence Data
  • Nucleic Acid Conformation*
  • RNA Precursors
  • RNA Splice Sites / genetics
  • RNA, Bacterial / chemistry*
  • RNA, Bacterial / genetics
  • RNA, Bacterial / metabolism*
  • RNA, Transfer, Ile / chemistry
  • RNA, Transfer, Ile / genetics*
  • Substrate Specificity

Substances

  • RNA Precursors
  • RNA Splice Sites
  • RNA, Bacterial
  • RNA, Transfer, Ile
  • Magnesium