HIV-1 modulates the tRNA pool to improve translation efficiency
Open accessAbstract
Despite its poorly adapted codon usage, HIV-1 replicates and is expressed extremely well in human host cells. HIV-1 has recently been shown to package non-lysyl transfer RNAs (tRNAs) in addition to the tRNALys needed for priming reverse transcription and integration of the HIV-1 genome. By comparing the codon usage of HIV-1 genes with that of its human host, we found that tRNAs decoding codons that are highly used by HIV-1 but avoided by its host are overrepresented in HIV-1 virions. In particular, tRNAs decoding A-ending codons, required for the expression of HIV's A-rich genome, are highly enriched. Because the affinity of Gag-Pol for all tRNAs is nonspecific, HIV packaging is most likely passive and reflects the tRNA pool at the time of viral particle formation. Codon usage of HIV-1 early genes is similar to that of highly expressed host genes, but codon usage of HIV-1 late genes was better adapted to the selectively enriched tRNA pool, suggesting that alterations in the tRNA pool are induced late in viral infection. If HIV-1 genes are adapting to an altered tRNA pool, codon adaptation of HIV-1 may be better than previously thought.
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HTLV-1 does not exhibit differences in codon adaptation between early and late genes.
“However, HTLV-1 does not exhibit differences in codon adaptation between early and late genes (99).”
From Role of host tRNAs and aminoacyl-tRNA synthetases in retroviral replication (2019) · cites this paper as [99]
HIV-1 early genes (tat, rev, nef) adapt to host codon usage better than late genes (gag, pol, env, vif, vpu, vpr), which contain a higher portion of rare codons.
“HIV-1 early genes (tat, rev, and nef) adapt to the host codon usage better than late genes (gag, pol, env, vif, vpu, and vpr), which contain a higher portion of rare codons (99).”
From Role of host tRNAs and aminoacyl-tRNA synthetases in retroviral replication (2019) · cites this paper as [99]
HIV-1 uses the host cell translational machinery to translate viral mRNAs but is poorly adapted to the codon usage of host cells.
“Although HIV-1 uses the host cell translational machinery to translate viral mRNAs, it is poorly adapted to the codon usage of host cells (99).”
From Role of host tRNAs and aminoacyl-tRNA synthetases in retroviral replication (2019) · cites this paper as [99]
There is a high frequency of A-ending codons in the protein-coding region of the HIV-1 genome, and these codons are under-represented in the host cell genome.
“In particular, there is a high frequency of A-ending codons in the protein-coding region of the HIV-1 genome, and these codons are under-represented in the host cell genome (99).”
From Role of host tRNAs and aminoacyl-tRNA synthetases in retroviral replication (2019) · cites this paper as [99]
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tRNAs as primer of reverse transcriptases
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Profiling non-lysyl tRNAs in HIV-1
Pavon-Eternod, M., Wei, M., Pan, T., & Kleiman, L. (2010) · RNA · doi:10.1261/rna.1928110 · Cited by 62 · see citing works
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Role of host tRNAs and aminoacyl-tRNA synthetases in retroviral replication
Jin, D., & Musier-Forsyth, K. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.rev118.002957 · Cited by 67 · see citing works
“However, HTLV-1 does not exhibit differences in codon adaptation between early and late genes (99).”
BackgroundInfluential
- Authors
- van Weringh, A., Ragonnet-Cronin, M., Pranckeviciene, E., Pavon-Eternod, M., Kleiman, L., & Xia, X.
- Affiliations
- Department of Biology, University of Ottawa, Ottawa, Ontario, Canada
- University of Chicago (US)
- Jewish General Hospital (CA)
- University of Ottawa (CA)
- Corresponding author
- Xia, Xuhua
- ORCID
- Xia, Xuhua
- Venue
- Molecular Biology and Evolution
- Publisher
- Oxford University Press (OUP)
- Published
- 2011-01-07
- Volume
- 28
- Issue
- 6
- Pages
- 1827-1834
- ISSN
- 0737-4038 (ISSN-L)
- 1537-1719
- PMC
- PMC3098512
- OpenAlex
- W2117312105
- Cited by
- 130
- References
- 3
- Citations by year
- 2026: 6 · 2025: 10 · 2024: 10 · 2023: 11 · 2022: 3 · 2021: 9 · 2020: 10 · 2019: 11 · 2018: 11 · 2017: 6 · 2016: 11 · 2015: 5 · 2014: 6 · 2013: 4 · 2012: 12
- FWCI
- 3.51
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Molecular Biology and Evolution (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- uO Research (University of Ottawa) (submittedVersion, public-domain)
- Vytautas Magnus University (submittedVersion)
- Funders
- Biotechnology and Biological Sciences Research Council (1098048)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Life Sciences › Immunology and Microbiology › Virology › HIV Research and Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Evolution and Genetic Dynamics
- Keywords
- HIV-1, tRNA pool, codon usage, translation efficiency, Gag-Pol, viral adaptation, late gene expression, viral particle formation
- MeSH terms
- Adaptation, Biological, Codon, Humans, RNA, Transfer, Protein Biosynthesis, HIV-1, HIV Infections, Gene Expression Regulation, Viral, Virus Assembly
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