Direct localization by cryo-electron microscopy of secondary structural elements in Escherichia coli 23 S rRNA which differ from the corresponding regions in Haloarcula marismortui

Rishi Matadeen, Petr Sergiev, Andrej Leonov, Tillmann Pape, Eli Van Der Sluis, Florian Mueller, Monika Osswald, Klaus Von Knoblauch, Richard Brimacombe, Alexey Bogdanov, Marin Van Heel, Olga Dontsova

Research output: Contribution to journalArticlepeer-review

9 Citations (Scopus)

Abstract

Insertions were introduced by a two-step mutagenesis procedure into each of five double-helical regions of Escherichia coli 23 S rRNA, so as to extend the helix concerned by 17 bp. The helices chosen were at sites within the 23 S molecule (h9, h25, h45, h63 and h98) where significant length variations between different species are known to occur. At each of these positions, with the exception of h45, there are also significant differences between the 23 S rRNAs of E. coli and Haloarcula marismortui. Plasmids carrying the insertions were introduced into an E. coli strain lacking all seven rrn operons. In four of the five cases the cells were viable and 50 S subunits could be isolated; only the insertion in h63 was lethal. The modified subunits were examined by cryo-electron microscopy (cryo-EM), with a view to locating extra electron density corresponding to the insertion elements. The results were compared both with the recently determined atomic structure of H. marismortui 23 S rRNA in the 50 S subunit, and with previous 23 S rRNA modelling studies based on cryo-EM reconstructions of E. coli ribosomes. The insertion element in h45 was located by cryo-EM at a position corresponding precisely to that of the equivalent helix in H. marismortui. The insertion in h98 (which is entirely absent in H. marismortui) was similarly located at a position corresponding precisely to that predicted from the E. coli modelling studies. In the region of h9, the difference between the E. coli and H. marismortui secondary structures is ambiguous, and the extra electron density corresponding to the insertion was seen at a location intermediate between the position of the nearest helix in the atomic structure and that in the modelled structure. In the case of h25 (which is about 50 nucleotides longer in H. marismortui), no clear extra cryo-EM density corresponding to the insertion could be observed.

Original languageEnglish
Pages (from-to)1341-1349
Number of pages9
JournalJournal of Molecular Biology
Volume307
Issue number5
DOIs
Publication statusPublished - 13 Apr 2001
Externally publishedYes

Keywords

  • 3D structure of rRNA
  • Cryo-electron microscopy
  • Phylogenetic variation
  • Site-directed mutagenesis
  • X-ray crystallography

Fingerprint

Dive into the research topics of 'Direct localization by cryo-electron microscopy of secondary structural elements in Escherichia coli 23 S rRNA which differ from the corresponding regions in Haloarcula marismortui'. Together they form a unique fingerprint.

Cite this