Correlation of the expansion segments in mammalian rRNA with the fine structure of the 80 S ribosome;: a cryoelectron microscopic reconstruction of the rabbit reticulocyte ribosome at 21 Å resolution

被引:61
作者
Dube, P
Bacher, G
Stark, H
Mueller, F
Zemlin, F
van Heel, M
Brimacombe, R
机构
[1] Max Planck Inst Mol Genet, D-14195 Berlin, Germany
[2] Max Planck Gesell, Fritz Haber Inst, D-14195 Berlin, Germany
[3] Zentrum Mol Biol, D-69120 Heidelberg, Germany
[4] Univ London Imperial Coll Sci Technol & Med, Dept Biochem, London SW7 2AY, England
关键词
cryoelectron microscopy; rRNA secondary structure; eukaroytic expansion segments; computer modelling; structure fitting;
D O I
10.1006/jmbi.1998.1804
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Samples of 80 S ribosomes from rabbit reticulocytes were subjected to electron cryomicroscopy combined with angular reconstitution. A three-dimensional reconstruction at 21 Angstrom resolution was obtained, which was compared with the corresponding (previously published) reconstruction of Escherichia coli 70 S ribosomes carrying tRNAs at the A and P sites. Ln the region of the intersubunit cavity, the principal features observed in the 70 S ribosome (such as the L1 protuberance, the central protuberance and A site finger in the large subunit) could all be clearly identified in the 80 S particle. On the other hand, significant additional features were observed in the 80 S ribosomes on the solvent sides and lower regions of both subunits. Ln the case of the small (40 S) subunit, the most prominent additions are two extensions at the base of the particle. By comparing the secondary structure of the rabbit 18 S rRNA with our model for the three-dimensional arrangement of E. coli 16 S rRNA, these two extensions could be correlated with the rabbit expansion segments (each totalling ca 170 bases) in the regions of helix 21, and of helices 8, 9 and 44, respectively. A similar comparison of the secondary structures of mammalian 28 S rRNA and E. coli 23 S rRNA, combined with preliminary modelling studies on the 23 S rRNA within the 50 S subunit, enabled the additional features in the 60 S subunit to be sub-divided into five groups. The first (corresponding to a total of ca 335 extra bases in helices 45, 98 and 101) is located on the solvent side of the 60 S subunit, close to the L7/L12 area. The second (820 bases in helices 25 and 38) is centrally placed on the solvent side of the subunit, whereas the third group (totaling 225 bases in helices 18/19, 27/29,52 and 54) lies towards the L1 side of the subunit. The fourth feature (80 bases in helices 78 and 79) Lies within or close to the L1 protuberance itself, and the fifth (560 bases in helix 63) is located underneath the L1 protuberance on the interface side of the 60 S subunit. (C) 1998 Academic Press Limited.
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页码:403 / 421
页数:19
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