A Major Controversy in Codon-Anticodon Adaptation Resolved by a New Codon Usage Index
Open accessAbstract
Two alternative hypotheses attribute different benefits to codon-anticodon adaptation. The first assumes that protein production is rate limited by both initiation and elongation and that codon-anticodon adaptation would result in higher elongation efficiency and more efficient and accurate protein production, especially for highly expressed genes. The second claims that protein production is rate limited only by initiation efficiency but that improved codon adaptation and, consequently, increased elongation efficiency have the benefit of increasing ribosomal availability for global translation. To test these hypotheses, a recent study engineered a synthetic library of 154 genes, all encoding the same protein but differing in degrees of codon adaptation, to quantify the effect of differential codon adaptation on protein production in Escherichia coli. The surprising conclusion that “codon bias did not correlate with gene expression” and that “translation initiation, not elongation, is rate-limiting for gene expression” contradicts the conclusion reached by many other empirical studies. In this paper, I resolve the contradiction by reanalyzing the data from the 154 sequences. I demonstrate that translation elongation accounts for about 17% of total variation in protein production and that the previous conclusion is due to the use of a codon adaptation index (CAI) that does not account for the mutation bias in characterizing codon adaptation. The effect of translation elongation becomes undetectable only when translation initiation is unrealistically slow. A new index of translation elongation ITE is formulated to facilitate studies on the efficiency and evolution of the translation machinery.
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Translation initiation is often the rate-limiting step.
“Optimum codon usage without efficient translation initiation does not increase protein production [10,11] because translation initiation is often the rate-limiting step.”
From Detailed Dissection and Critical Evaluation of the Pfizer/BioNTech and Moderna mRNA Vaccines (2021) · cites this paper as [11]
The Conceptual Framework says that inefficient initiation can limit the benefit of improved codon adaptation. But the Discussion concludes that both initiation and elongation limit translation efficiency, and notes that the low-initiation group studied is not representative of most genes. The paper therefore does not establish that initiation is often the rate-limiting step. (LLM, conf=0.83)
Experimental — accuracy not yet measuredThe codon optimization applied to BNT-162b2 and mRNA-1273 leads to a much increased CAI and ITE for the two vaccine mRNAs.
“The codon optimization applied to BNT-162b2 and mRNA-1273 leads to a much increased codon adaptation index (CAI) [21,22] and index of translation efficiency (ITE) [11,36] for the two vaccine mRNAs.”
From Detailed Dissection and Critical Evaluation of the Pfizer/BioNTech and Moderna mRNA Vaccines (2021) · cites this paper as [11]
Translation elongation becomes rate-limiting when translation initiation is highly efficient.
“Translation elongation becomes rate-limiting when translation initiation is highly efficient [10,11].”
From Detailed Dissection and Critical Evaluation of the Pfizer/BioNTech and Moderna mRNA Vaccines (2021) · cites this paper as [11]
Optimum codon usage without efficient translation initiation does not increase protein production.
“Optimum codon usage without efficient translation initiation does not increase protein production [10,11] because translation initiation is often the rate-limiting step.”
From Detailed Dissection and Critical Evaluation of the Pfizer/BioNTech and Moderna mRNA Vaccines (2021) · cites this paper as [11]
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Sharp, P. M., & Li, W.-H. (1987) · Nucleic Acids Research · doi:10.1093/nar/15.3.1281 · Cited by 3,992 · see citing works
Translation efficiency is determined by both codon bias and folding energy
Tuller, T., Waldman, Y. Y., Kupiec, M., & Ruppin, E. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0909910107 · Cited by 584 · cited 4× · see citing works
“The problem with the second assumption has been pointed out recently (Supek and Smuc 2010); Tuller et al. (2010) reanalyzed the data in addition to providing an overwhelming amount of additional empirical evidence to demonstrate the joint effect of both translation initiation and translation…”
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Detailed Dissection and Critical Evaluation of the Pfizer/BioNTech and Moderna mRNA Vaccines
Xia, X. (2021) · Vaccines · doi:10.3390/vaccines9070734 · Cited by 201 · see citing works
Self-citation
- Authors
- Xia, X.
- Affiliations
- University of Ottawa (CA)
- Corresponding author
- Xia, Xuhua
- ORCID
- Xia, Xuhua
- Venue
- Genetics
- Publisher
- Oxford University Press (OUP)
- Published
- 2014-12-05
- Volume
- 199
- Issue
- 2
- Pages
- 573-579
- ISSN
- 0016-6731 (ISSN-L)
- 1943-2631
- PMC
- PMC4317663
- OpenAlex
- W2146837785
- Cited by
- 67
- References
- 2
- Citations by year
- 2026: 6 · 2025: 2 · 2024: 4 · 2023: 5 · 2022: 4 · 2021: 4 · 2020: 8 · 2019: 5 · 2018: 11 · 2017: 6 · 2016: 8 · 2015: 4
- FWCI
- 2.27
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model (vor)
- Locations
- Genetics (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Evolution and Genetic Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Keywords
- codon usage bias, codon adaptation index, translation initiation, protein production rate, gene expression, Escherichia coli, mutational bias
- MeSH terms
- Adaptation, Biological, Anticodon, Codon, Selection, Genetic, Protein Biosynthesis, Evolution, Molecular
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