Title of article :
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
Author/Authors :
Rishi Matadeen، نويسنده , , Petr Sergiev، نويسنده , , Andrej Leonov، نويسنده , , Tillmann Pape، نويسنده , , Eli van der Sluis، نويسنده , , Florian Mueller، نويسنده , , Monika Osswald، نويسنده , , Klaus von Knoblauch، نويسنده , , Richard Brimacombe and Marin van Heel، نويسنده , , Alexey Bogdanov، نويسنده , , Marin van Heel، نويسنده , , Olga Dontsova، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2001
Pages :
9
From page :
1341
To page :
1349
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.
Keywords :
X-ray crystallography , phylogenetic variation , site-directed mutagenesis , 3D structure of rRNA , cryo-electron microscopy
Journal title :
Journal of Molecular Biology
Serial Year :
2001
Journal title :
Journal of Molecular Biology
Record number :
1240693
Link To Document :
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