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An arc of unpaired "hinge bases" facilitates information exchange among functional centers of the ribosome.

Abstract
Information must be shared and functions coordinated among the spatially distinct functional centers of the ribosome. To address these issues, a yeast-based genetic system enabling generation of stable strains expressing only mutant forms of rRNA was devised. The B1a bridge (helix 38) has been implicated in the subtle modulation of numerous ribosomal functions. Base-specific mutations were introduced into helix 38 at sites affecting the B1a bridge and where it contacts the aminoacyl-tRNA (aa-tRNA) D-loop. Both sets of mutants promoted increased affinities for aa-tRNA but had different effects in their responses to two A-site-specific drugs and on suppression nonsense codons. Structural analyses revealed an arc of nucleotides in 25S rRNA that link the B1a bridge, the peptidyltransferase center, the GTPase-associated center, and the sarcin/ricin loop. We propose that a series of regularly spaced "hinge bases" provide fulcrums around which rigid helices can reorient themselves depending on the occupancy status of the A-site.
AuthorsRasa Rakauskaite, Jonathan D Dinman
JournalMolecular and cellular biology (Mol Cell Biol) Vol. 26 Issue 23 Pg. 8992-9002 (Dec 2006) ISSN: 0270-7306 [Print] United States
PMID17000775 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
Chemical References
  • Codon, Nonsense
  • RNA, Bacterial
  • RNA, Fungal
  • RNA, Ribosomal
  • RNA, Transfer, Amino Acyl
  • RNA, ribosomal, 25S
  • RNA, Transfer
  • Peptidyl Transferases
Topics
  • Base Sequence
  • Codon, Nonsense
  • Escherichia coli (genetics)
  • Models, Molecular
  • Mutation
  • Nucleic Acid Conformation
  • Peptidyl Transferases (chemistry, metabolism)
  • Plasmids (metabolism)
  • RNA, Bacterial (genetics)
  • RNA, Fungal (genetics)
  • RNA, Ribosomal (chemistry, genetics, metabolism)
  • RNA, Transfer (genetics, metabolism)
  • RNA, Transfer, Amino Acyl (metabolism)
  • Ribosomes (chemistry, genetics, metabolism)
  • Saccharomyces cerevisiae (genetics)
  • Structure-Activity Relationship

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