Evidence map›Paper›PMID 11416124›Full record

ArticleMolecular and cellular biology2001

Phosphorylation of MafA is essential for its transcriptional and biological properties.

S Benkhelifa, S Provot, E Nabais, A Eychène, G Calothy, M P Felder-Schmittbuhl

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

52 citing papers in PubMed, 91 citations in OpenAlex.

  1. Review
  2. Article
  3. Macrophage re-programming by JAK inhibitors relies on MAFB.Cellular and molecular life sciences : CMLS · 2024
    Article
  4. Modelling human diabetesFrontiers in endocrinology · 2024
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  15. CMIP is oncogenic in human gastric cancer cells.Molecular medicine reports · 2017
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review
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

6 authors at 2 institutions in 1 country.

S BenkhelifaUMR 146 CNRS-Institut Curie, Centre Universitaire, 91405 Orsay cedex, France.
S Provot
E Nabais
A Eychène
G Calothy
M P Felder-Schmittbuhl
Centre National de la Recherche Scientifique · FRInstitut Curie · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We previously described the identification of quail MafA, a novel transcription factor of the Maf bZIP (basic region leucine zipper) family, expressed in the differentiating neuroretina (NR). In the present study, we provide the first evidence that MafA is phosphorylated and that its biological properties strongly rely upon phosphorylation of serines 14 and 65, two residues located in the transcriptional activating domain within a consensus for phosphorylation by mitogen-activated protein kinases and which are conserved among Maf proteins. These residues are phosphorylated by ERK2 but not by p38, JNK, and ERK5 in vitro. However, the contribution of the MEK/ERK pathway to MafA phosphorylation in vivo appears to be moderate, implicating another kinase. The integrity of serine 14 and serine 65 residues is required for transcriptional activity, since their mutation into alanine severely impairs MafA capacity to activate transcription. Furthermore, we show that the MafA S14A/S65A mutant displays reduced capacity to induce expression of QR1, an NR-specific target of Maf proteins. Likewise, the integrity of serines 14 and 65 is essential for the MafA ability to stimulate expression of crystallin genes in NR cells and to induce NR-to-lens transdifferentiation. Thus, the MafA capacity to induce differentiation programs is dependent on its phosphorylation.

Indexed as

Leucine ZippersAmino Acid SequenceAnimalsBinding SitesEye ProteinsGlycoproteinsHeLa CellsHumansLectins, C-TypeLens, CrystallineMaf Transcription Factors, LargeMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Mitogen-Activated Protein Kinase 7Mitogen-Activated Protein Kinase 8Mitogen-Activated Protein KinasesEye ProteinsGlycoproteinsKLRG1 protein, humanLectins, C-TypeMAFA protein, humanMaf Transcription Factors, LargeMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Mitogen-Activated Protein Kinase 7Mitogen-Activated Protein Kinase 8Mitogen-Activated Protein Kinasesp38 Mitogen-Activated Protein KinasesPhosphoproteinsProto-Oncogene ProteinsQR1 protein, Coturnix japonicaReceptors, ImmunologicSerineTrans-Activators

Identifiers

PMID11416124
PMCPMC87104
OpenAlexW2165632078

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.