Structure of the chloroplast ribosome: Novel domains for translation regulation

被引:65
作者
Manuell, Andrea L.
Quispe, Joel
Mayfield, Stephen P. [1 ]
机构
[1] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA USA
[3] Scripps Res Inst, Natl Resource Automated Mol Microscopy, La Jolla, CA USA
关键词
D O I
10.1371/journal.pbio.0050209
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
Gene expression in chloroplasts is controlled primarily through the regulation of translation. This regulation allows coordinate expression between the plastid and nuclear genomes, and is responsive to environmental conditions. Despite common ancestry with bacterial translation, chloroplast translation is more complex and involves positive regulatory mRNA elements and a host of requisite protein translation factors that do not have counterparts in bacteria. Previous proteomic analyses of the chloroplast ribosome identified a significant number of chloroplast-unique ribosomal proteins that expand upon a basic bacterial 70S-like composition. In this study, cryo-electron microscopy and single-particle reconstruction were used to calculate the structure of the chloroplast ribosome to a resolution of 15.5 angstrom. Chloroplast-unique proteins are visualized as novel structural additions to a basic bacterial ribosome core. These structures are located at optimal positions on the chloroplast ribosome for interaction with mRNAs during translation initiation. Visualization of these chloroplast-unique structures on the ribosome, combined with mRNA cross-linking, allows us to propose a model for translation initiation in chloroplasts in which chloroplast-unique ribosomal proteins interact with plastid-specific translation factors and RNA elements to facilitate regulated translation of chloroplast mRNAs.
引用
收藏
页码:1785 / 1797
页数:13
相关论文
共 71 条
[41]   UCSF chimera - A visualization system for exploratory research and analysis [J].
Pettersen, EF ;
Goddard, TD ;
Huang, CC ;
Couch, GS ;
Greenblatt, DM ;
Meng, EC ;
Ferrin, TE .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 2004, 25 (13) :1605-1612
[42]   OCCURRENCE AND SPACING OF RIBOSOME RECOGNITION SITES IN MESSENGER-RNAS OF CHLOROPLASTS FROM HIGHER-PLANTS [J].
RUF, M ;
KOSSEL, H .
FEBS LETTERS, 1988, 240 (1-2) :41-44
[43]   Structure of the E-coli signal recognition particle bound to a translating ribosome [J].
Schaffitzel, Christiane ;
Oswald, Miro ;
Berger, Imre ;
Ishikawa, Takashi ;
Abrahams, Jan Pieter ;
Koerten, Henk K. ;
Koning, Roman I. ;
Ban, Nenad .
NATURE, 2006, 444 (7118) :503-506
[44]   Structural basis for the interaction of antibiotics with the peptidyl transferase centre in eubacteria [J].
Schlünzen, F ;
Zarivach, R ;
Harms, J ;
Bashan, A ;
Tocilj, A ;
Albrecht, R ;
Yonath, A ;
Franceschi, F .
NATURE, 2001, 413 (6858) :814-821
[45]   Structural analysis of kasugamycin inhibition of translation [J].
Schuwirth, Barbara S. ;
Day, J. Michael ;
Hau, Cathy W. ;
Janssen, Gary R. ;
Dahlberg, Albert E. ;
Cate, Jamie H. Doudna ;
Vila-Sanjurjo, Anton .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2006, 13 (10) :879-886
[46]   Structures of the bacterial ribosome at 3.5 Å resolution [J].
Schuwirth, BS ;
Borovinskaya, MA ;
Hau, CW ;
Zhang, W ;
Vila-Sanjurjo, A ;
Holton, JM ;
Cate, JHD .
SCIENCE, 2005, 310 (5749) :827-834
[47]   Visualization of protein S1 within the 30S ribosomal subunit and its interaction with messenger RNA [J].
Sengupta, J ;
Agrawal, RK ;
Frank, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (21) :11991-11996
[48]   Structure of the mammalian mitochondrial ribosome reveals an expanded functional role for its component proteins [J].
Sharma, MR ;
Koc, EC ;
Datta, PP ;
Booth, TM ;
Spremulli, LL ;
Agrawal, RK .
CELL, 2003, 115 (01) :97-108
[49]   A nuclear gene of Chlamydomonas reinhardtii, Tba1, encodes a putative oxidoreductase required for translation of the chloroplast psbA mRNA [J].
Somanchi, A ;
Barnes, D ;
Mayfield, SP .
PLANT JOURNAL, 2005, 42 (03) :341-352
[50]   Cryo-EM visualization of a viral internal ribosome entry site bound to human ribosomes: The IRES functions as an RNA-Based translation factor [J].
Spahn, CMT ;
Jan, E ;
Mulder, A ;
Grassucci, RA ;
Sarnow, P ;
Frank, J .
CELL, 2004, 118 (04) :465-475