Evidence map›Paper›PMID 7799942›Full record

ArticleMolecular and cellular biology1995

Alternative translation of human fibroblast growth factor 2 mRNA occurs by internal entry of ribosomes.

S Vagner, M C Gensac, A Maret, F Bayard, F Amalric, H Prats, A C Prats

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 127 papers.

0numbers the graph read from it
0cells of the map it votes in
127citing papers in PubMed
8.5field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

127 citing papers in PubMed, 335 citations in OpenAlex.

  1. Review
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  4. Article
  5. Long non-coding RNAeLife · 2022
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  11. Review
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  14. IRES Trans-Acting Factors, Key Actors of the Stress Response.International journal of molecular sciences · 2019
    Review
  15. Cap-Independent mRNA Translation in Germ Cells.International journal of molecular sciences · 2019
    Review
  16. Review
  17. Review
  18. Review
  19. Review
  20. Internal ribosome entry site-based vectors for combined gene therapy.World journal of experimental medicine · 2015
    Review

67 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

S VagnerINSERM U397, Endocrinologie et Communication Cellulaire, Institut Louis Bugnard, Centre Hospitalier Universitaire de Rangueil, Toulouse, France.
M C Gensac
A Maret
F Bayard
F Amalric
H Prats
A C Prats
Inserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alternative initiations of translation of the human fibroblast growth factor 2 (FGF-2) mRNA, at three CUG start codons and one AUG start codon, result in the synthesis of four isoforms of FGF-2. This process has important consequences on the fate of FGF-2: the CUG-initiated products are nuclear and their constitutive expression is able to induce cell immortalization, whereas the AUG-initiated product, mostly cytoplasmic, can generate cell transformation. Thus, the different isoforms probably have distinct targets in the cell. We show here that translation initiation of the FGF-2 mRNA breaks the rule of the cap-dependent ribosome scanning mechanism. First, translation of the FGF-2 mRNA was shown to be cap independent in vitro. This cap-independent translation required a sequence located between nucleotides (nt) 192 and 256 from the 5' end of the 318-nt-long 5' untranslated region. Second, expression of bicistronic vectors in COS-7 cells indicated that the FGF-2 mRNA is translated through a process of internal ribosome entry mediated by the mRNA leader sequence. By introducing additional AUG codons into the RNA leader sequence, we localized an internal ribosome entry site to between nt 154 and 318 of the 5' untranslated region, just upstream of the first CUG. The presence of an internal ribosome entry site in the FGF-2 mRNA suggests that the process of internal translation initiation, by controlling the expression of a growth factor, could have a crucial role in the control of cell proliferation and differentiation.

Indexed as

Peptide Chain Initiation, TranslationalAnimalsBase SequenceChlorocebus aethiopsDNA PrimersEukaryotic Initiation Factor-4EFibroblast Growth Factor 2Gene Expression RegulationHumansIn Vitro TechniquesMolecular Sequence DataPeptide Initiation FactorsRegulatory Sequences, Nucleic AcidRibosomesRNA CapsRNA, MessengerDNA PrimersEukaryotic Initiation Factor-4EFibroblast Growth Factor 2Peptide Initiation FactorsRNA CapsRNA, Messenger

Identifiers

PMID7799942
PMCPMC231905
OpenAlexW2105554008

What OpenQuestion holds

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Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.