Evidence map›Paper›PMID 23396363›Full record

ArticleOncogene2014

SUMOylation of the inducible (c-Fos:c-Jun)/AP-1 transcription complex occurs on target promoters to limit transcriptional activation.

D Tempé, E Vives, F Brockly, H Brooks, S De Rossi, M Piechaczyk, G Bossis

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

30 citing papers in PubMed, 60 citations in OpenAlex.

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  16. LncRNAs in the Type I Interferon Antiviral Response.International journal of molecular sciences · 2020
    Review
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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 5 institutions in 1 country.

D Tempé1] Equipe labellisée Ligue contre le Cancer, Institut de Génétique Moléculaire de Montpellier, UMR 5535, CNRS, Montpellier, France [2] Université Montpellier 2, Place Eugène Bataillon, Montpellier, France [3] Université Montpellier 1, 5 Bd Henri IV, Montpellier, France.
E Vives1] IRCM, Institut de Recherche en Cancérologie de Montpellier, Montpellier, France [2] Université Montpellier 1, INSERM U896, Montpellier, France [3] CRLC Val d'Aurelle Paul Lamarque, Montpellier, France.
F Brockly1] Equipe labellisée Ligue contre le Cancer, Institut de Génétique Moléculaire de Montpellier, UMR 5535, CNRS, Montpellier, France [2] Université Montpellier 2, Place Eugène Bataillon, Montpellier, France [3] Université Montpellier 1, 5 Bd Henri IV, Montpellier, France.
H Brooks1] Equipe labellisée Ligue contre le Cancer, Institut de Génétique Moléculaire de Montpellier, UMR 5535, CNRS, Montpellier, France [2] Université Montpellier 2, Place Eugène Bataillon, Montpellier, France [3] Université Montpellier 1, 5 Bd Henri IV, Montpellier, France.
S De RossiMontpellier RIO Imaging, BIOCAMPUS Montpellier, 141, rue de la cardonille, Montpellier, France.
M Piechaczyk1] Equipe labellisée Ligue contre le Cancer, Institut de Génétique Moléculaire de Montpellier, UMR 5535, CNRS, Montpellier, France [2] Université Montpellier 2, Place Eugène Bataillon, Montpellier, France [3] Université Montpellier 1, 5 Bd Henri IV, Montpellier, France.
G Bossis1] Equipe labellisée Ligue contre le Cancer, Institut de Génétique Moléculaire de Montpellier, UMR 5535, CNRS, Montpellier, France [2] Université Montpellier 2, Place Eugène Bataillon, Montpellier, France [3] Université Montpellier 1, 5 Bd Henri IV, Montpellier, France.
Centre National de la Recherche Scientifique · FRUniversité de Montpellier · FRBioCampus MontpellierInstitut de Génétique Moléculaire de Montpellier · FRInstitut de Recherche en Cancérologie de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The inducible proto-oncogenic (c-Fos:c-Jun)/AP-1 transcription complex binds 12-O-tetradecanoylphorbol 13-acetate (TPA)-responsive elements (TRE) in its target genes. It is tightly controlled at multiple levels to avoid the deleterious effects of its inappropriate activation. In particular, SUMOylation represses its transactivation capacity in transient reporter assays using constitutively expressed proteins. This led to the presumption that (c-Fos:c-Jun)/AP-1 SUMOylation would be required to turn-off transcription of its target genes, as proposed for various transcription factors. Instead, thanks to the generation of an antibody specific for SUMO-modified c-Fos, we provide here direct evidence that SUMOylated c-Fos is present on a stably integrated reporter TPA-inducible promoter at the onset of transcriptional activation and colocalizes with RNA polymerase II within chromatin. Interestingly, (c-Fos:c-Jun)/AP-1 SUMOylation limits reporter gene induction, as well as the appearance of active transcription-specific histone marks on its promoter. Moreover, non-SUMOylatable mutant (c-Fos:c-Jun)/AP-1 dimers accumulate to higher levels on their target promoter, suggesting that SUMOylation might facilitate the release of (c-Fos:c-Jun)/AP-1 from promoters. Finally, activation of GADD153, an AP-1 target gene, is also associated with a rapid increase in SUMOylation at the level of its TRE and c-Fos SUMOylation dampens its induction by TPA. Taken together, our data suggest that SUMOylation could serve to buffer transcriptional activation of AP-1 target genes.

Indexed as

SumoylationTranscriptional ActivationBase SequenceHEK293 CellsHumansJNK Mitogen-Activated Protein KinasesPromoter Regions, GeneticProtein BindingProtein TransportProto-Oncogene Proteins c-fosRNA Polymerase IIRNA, Small InterferingSmall Ubiquitin-Related Modifier ProteinsTranscription Factor AP-1Transcription, GeneticJNK Mitogen-Activated Protein KinasesProto-Oncogene Proteins c-fosRNA Polymerase IIRNA, Small InterferingSmall Ubiquitin-Related Modifier ProteinsSUMO2 protein, humanTranscription Factor AP-1

Identifiers

PMID23396363
OpenAlexW2082353756

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.