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The Ribosome: Some Hard Facts about Its Structure and Hot Air about Its Evolution
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Ribosomes from all species consist of approximately two-thirds RNA and one-third protein.Ribosomes from mammalian mitochondria are an exception, with the ratio of protein and RNA reversed (see Sharma et al. 2003).All ribosomes consist of two subunits, termed 50S and 30S in bacteria or 60S and 40S in eukaryotes.Together, they comprise the 70S ribosome in bacteria or the 80S ribosome in eukaryotes (Fig. 1A).The mRNA containing the genetic template binds in a cleft in the small subunit.The amino acids themselves are brought into the ribosome by aminoac ylated tRNA substrates.The ribosome has three binding sites for tRNA: the A (aminoacyl) site that brings the new aminoacyl tRNA, the P (peptidyl) site that holds the nascent peptide chain, and the E (exit) site to which the deacylated P-site tRNA moves after peptide bond formation (Fig. 1B).Translation in all species can be divided into three stages (Fig. 2) (for review, see Schmeing and Ram a krishnan 2009).During initiation, the small subunit of the ribosome binds mRNA at the start site of the coding sequence, in a precise manner that puts the start codon in the P site.This requires three initiation factors and a special initiator tRNA that binds to the P site.Initiation is followed by the elongation cycle, which consists of three important steps: decoding, peptidyl transfer, and translocation.During decoding, the correct aminoacyl tRNA, which is delivered to the A site of the ribosome as a ternary complex with elongation factor Tu (EF-Tu) and GTP, is selected based on the codon on the mRNA in the A site.Selection of the tRNA leads to hydrolysis of GTP by EF-Tu and release of the factor from the ribosome.The aminoacyl end of the selected tRNA then swings into the peptidyl transferase center (PTC) in the 50S subunit of the ribosome, where peptide bond formation occurs rapidly and spontaneously.*The title is a paraphrase of one by the late eminent crystallographer David M. Blow: "Hard facts on structure: Hot air about mobility" (Nature [1982] 297: 454-455).
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Recent structures of ribosomes have unambiguously shown that the essential functions of the ribosome, such as decoding, peptidyl transfer, and translocation, all appear to be mediated by RNA.
“Recent structures of ribosomes have unambiguously shown that the essential functions of the ribosome, such as decoding, peptidyl transfer, and translocation, all appear to be mediated by RNA [91].”
From The Origin of Prebiotic Information System in the Peptide/RNA World: A Simulation Model of the Evolution of Translation and the Genetic Code (2019) · cites this paper as [91]
Citations
Cites
Unusual Resistance of Peptidyl Transferase to Protein Extraction Procedures
Noller, H. F., Hoffarth, V., & Zimniak, L. (1992) · Science · doi:10.1126/science.1604315 · Cited by 728
The ribosome as an entropy trap
Sievers, A., Beringer, M., Rodnina, M. V., & Wolfenden, R. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0402488101 · Cited by 357
A hierarchical model for evolution of 23S ribosomal RNA
Bokov, K., & Steinberg, S. V. (2009) · Nature · doi:10.1038/nature07749 · Cited by 228
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Prebiotic Systems Chemistry: New Perspectives for the Origins of Life
Ruiz-Mirazo, K., Briones, C., & de la Escosura, A. (2014) · Chemical Reviews · doi:10.1021/cr2004844 · Cited by 930
Cech, T. R. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a006742 · Cited by 244
Chatterjee, S., & Yadav, S. (2019) · Life · doi:10.3390/life9010025 · Cited by 80
“Because the number of proteins greatly exceeded the number of RNA domains, it can hardly come as a surprise that every rRNA domain interacted with multiple proteins in ribosomes [91].”
Background
Metadata
- Authors
- Ramakrishnan, V.
- Affiliations
- MRC Laboratory of Molecular Biology (GB)
- Corresponding author
- Ramakrishnan, V.
- ORCID
- Ramakrishnan, V.
- Venue
- Cold Spring Harbor Symposia on Quantitative Biology
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2009-01-01
- Volume
- 74
- Issue
- 0
- Pages
- 25-33
- ISSN
- 0091-7451 (ISSN-L)
- 1943-4456
- OpenAlex
- W2128420193
- Cited by
- 27
- References
- 3
- Citations by year
- 2025: 1 · 2024: 2 · 2023: 1 · 2022: 2 · 2019: 4 · 2018: 3 · 2015: 1 · 2014: 3 · 2013: 2 · 2012: 4
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Cold Spring Harbor Symposia on Quantitative Biology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Agouron Institute
- Wellcome Trust
- Louis-Jeantet Foundation
- Medical Research Council
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA modifications and cancer
- Physical Sciences › Physics and Astronomy › Astronomy and Astrophysics › Origins and Evolution of Life
- Keywords
- ribosome structure, ribosome evolution, ribosomal RNA, ribosomal proteins, ribosomal subunits, ribosome binding site, translation initiation, peptidyl transferase center, ribosome crystal structure, ribosome function, ribosome assembly
- MeSH terms
- Models, Molecular, Ribosomes, RNA, Protein Biosynthesis, Molecular Structure, Evolution, Molecular
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