The Relationship between Eukaryotic Translation and mRNA Stability
Open accessAbstract
A new strategy was developed to study the relationship between the translation and degradation of a specific mRNA in the yeast Saccharomyces cerevisiae. A series of 5'-untranslated regions (UTR) was combined with the cat gene from the bacterial transposon Tn9, allowing us to test the influence of upstream open reading frames (uORFs) on translation and mRNA stability. The 5'-UTR sequences were designed so that the minimum possible sequence alteration, a single nucleotide substitution, could be used to create a 7-codon ORF upstream of the cat gene. The uORF was translated efficiently, but at the same time inhibited translation of the cat ORF and destabilized the cat mRNA. Investigations of various derivatives of the 5'-UTR indicated that cat translation was primarily attributable to leaky scanning of ribosomes past the uORF rather than to reinitiation. Therefore, these data directly demonstrate destabilization of a specific mRNA linked to changes in translational initiation on the same transcript. In contrast to the previously proposed nonsense-mediated mRNA decay pathway, destabilization was not triggered by premature translational termination in the main ORF and was not discernibly dependent upon a reinitiation-driven mechanism. This suggests the existence of an as yet not described pathway of translation-linked mRNA degradation.
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A poly(A) tail of 120 units is considered the standard size for mRNA vaccines.
“A poly(A) tail of 120 units is considered the standard size for mRNA vaccines.9,20,21”
From Combining an optimized mRNA template with a double purification process allows strong expression of in vitro transcribed mRNA (2021) · cites this paper as [20]
The Materials and Methods and Results passages discuss yeast cat mRNA constructs and translation, not mRNA vaccines. Searches for “poly(A),” “120 units,” and vaccine-related tail length found no passage in our copy addressing a standard poly(A)-tail size for mRNA vaccines. (LLM, conf=0.75)
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- Authors
- Oliveira, C. C., & McCarthy, J. E. G.
- Affiliations
- Helmholtz Centre for Infection Research (DE)
- Corresponding author
- McCarthy, John E.G.
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 1995-04
- Volume
- 270
- Issue
- 15
- Pages
- 8936-8943
- ISSN
- 0021-9258 (ISSN-L)
- OpenAlex
- W2019025253
- Cited by
- 121
- References
- 0
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 1 · 2023: 3 · 2022: 3 · 2021: 7 · 2020: 1 · 2019: 4 · 2018: 1 · 2017: 1 · 2016: 2 · 2015: 2 · 2014: 2 · 2013: 6 · 2012: 3
- FWCI
- 3.22
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- PubMed (publishedVersion)
- 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 Research and Splicing
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Keywords
- mRNA stability, translation (biology), upstream open reading frames, 5' untranslated region, leaky scanning, nonsense-mediated mRNA decay, cat gene, Saccharomyces cerevisiae, ribosome scanning
- MeSH terms
- Base Sequence, Half-Life, Hydrolysis, Molecular Sequence Data, RNA, Fungal, RNA, Messenger, Saccharomyces cerevisiae, Protein Biosynthesis, Chloramphenicol O-Acetyltransferase, Open Reading Frames
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