Cited by 121RNA and protein synthesis mechanismsRNA Research and SplicingFungal and yeast genetics research

The Relationship between Eukaryotic Translation and mRNA Stability

Open access
Oliveira, Carla C., McCarthy, John E.G.·1995·Journal of Biological Chemistry

Abstract

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.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1074/jbc.270.15.8936

Cites

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • 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)

    Experimental — accuracy not yet measured

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

No references could be resolved yet.

Research works printed but not linked: 13

  1. [1]1. Sachs, A.B. Cell. 1993; 74:413-421 Full Text (PDF) Scopus (839) PubMed Google Scholar
  2. [2]2. Belasco, J. ∙ Brawerman, G. (Editors) Control of Messenger RNA Stability Academic Press, San Diego, 1993 Google Scholar
  3. [3]3. Caponigro, G. ∙ Muhlrad, D. ∙ Parker, R. Mol. Cell. Biol. 1993; 13:5141-5148 Crossref Scopus (158) PubMed Google Scholar
  4. [4]4. Wellington, C. ∙ Greenberg, M.E. ∙ Belasco, J.G. Mol. Cell. Biol. 1993; 13:5034-5042 Crossref Scopus (69) PubMed Google Scholar
  5. [5]5. Losson, R. ∙ Lacroute, F. Proc. Natl. Acad. Sci. U. S. A. 1979; 76:5134-5137 Crossref Scopus (348) PubMed Google Scholar
  6. [6]6. Pelsey, F. ∙ Lacroute, F. Curr. Genet. 1984; 8:277-282 Crossref Scopus (42) PubMed Google Scholar
  7. [7]7. Peltz, S.W. ∙ Brown, A. ∙ Jacobson, A. Genes & Dev. 1993; 7:1737-1754 Crossref Scopus (253) PubMed Google Scholar
  8. [8]8. Cheng, J. ∙ Maquat, L. Mol. Cell. Biol. 1993; 13:1892-1902 Crossref Scopus (174) PubMed Google Scholar
  9. [9]9. Leeds, P. ∙ Wood, J.M. ∙ Lee, B.-S. ... Mol. Cell. Biol. 1992; 12:2165-2177 Crossref Scopus (263) PubMed Google Scholar
  10. [10]10. Peltz, S.W. ∙ Trotta, C. ∙ Feng, H. ... Brown, A.J.P. ∙ Tuite, M.F. ∙ McCarthy, J.E.G. (Editors) Protein Synthesis and Targeting in Yeast Springer-Verlag, Berlin, Germany, 1993; 1-10 Crossref Google Scholar
  11. [11]11. Herrick, D. ∙ Parker, R. ∙ Jacobson, A. Mol. Cell. Biol. 1990; 10:2269-2284 Crossref Scopus (324) PubMed Google Scholar
  12. [12]12. Peltz, S.W. ∙ Donahue, J.L. ∙ Jacobson, A. Mol. Cell. Biol. 1992; 12:5778-5784 Crossref Scopus (69) PubMed Google Scholar
  13. [13]13. Stevens, A. J. Biol. Chem. 1980; 255:3080-3085

Cited by

Sorted by citations

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
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

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review