Evidence map›Paper›PMID 15964820›Full record

ArticleMolecular and cellular biology2005

Arginine methylation provides epigenetic transcription memory for retinoid-induced differentiation in myeloid cells.

Balint L Balint, Attila Szanto, Andras Madi, Uta-Maria Bauer, Petra Gabor, Szilvia Benko, Laszlo G Puskás, Peter J A Davies, Laszlo Nagy

Abstract read
In one paragraph

Article in Molecular and cellular biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.5field-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

28 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Protein arginine hypomethylation in a mouse model of cystathionine β-synthase deficiency.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2014
    Article
  11. Article
  12. Article
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  14. Review
  15. Article
  16. Article
  17. Cellular functions of tissue transglutaminase.International review of cell and molecular biology · 2012
    Review
  18. Article
  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

9 authors at 4 institutions in 3 countries.

Balint L BalintDepartment of Biochemistry and Molecular Biology, Research Center for Molecular Medicine, University of Debrecen, Medical and Health Science Center, Nagyerdei krt. 98, Debrecen H-4012, Hungary.
Attila Szanto
Andras Madi
Uta-Maria Bauer
Petra Gabor
Szilvia Benko
Laszlo G Puskás
Peter J A Davies
Laszlo Nagy
University of Debrecen · HUHungarian Academy of Sciences · HUPhilipps University of Marburg · DEThe University of Texas Health Science Center at Houston · US

Funding

CHROMATIN ACTIVATION IN RETINOID-INDUCED APOPTOSISR03TW001146 · FIC · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI DAVIES, PETER J · 1999 to 2001
$79k
FIC NIH HHS 5RO3 TW 01146-02Wellcome Trust
6 · The paper itself

Abstract

Cellular differentiation is governed by changes in gene expression, but at the same time, a cell's identity needs to be maintained through multiple cell divisions during maturation. In myeloid cell lines, retinoids induce gene expression and a well-characterized two-step lineage-specific differentiation. To identify mechanisms that contribute to cellular transcriptional memory, we analyzed the epigenetic changes taking place on regulatory regions of tissue transglutaminase, a gene whose expression is tightly linked to retinoid-induced differentiation. Here we report that the induction of an intermediary or "primed" state of myeloid differentiation is associated with increased H4 arginine 3 and decreased H3 lysine 4 methylation. These modifications occur before transcription and appear to prime the chromatin for subsequent hormone-regulated transcription. Moreover, inhibition of methyltransferase activity, pre-acetylation, or activation of the enzyme PAD4 attenuated retinoid-regulated gene expression, while overexpression of PRMT1, a methyltransferase, enhanced retinoid responsiveness. Taken together, our results suggest that H4 arginine 3 methylation is a bona fide positive epigenetic marker and regulator of transcriptional responsiveness as well as a signal integration mechanism during cell differentiation and, as such, may provide epigenetic memory.

Indexed as

DNA MethylationEpigenesis, GeneticTranscription, GeneticAcetylationArginineCell DifferentiationCell LineageChromatinGene Expression RegulationGenetic MarkersHistonesHL-60 CellsHumansHydrolasesIonophoresModels, BiologicalArginineChromatinGenetic MarkersHistonesHydrolasesIonophoresPADI4 protein, humanProtein-Arginine DeiminasesProtein-Arginine Deiminase Type 4Protein-Arginine N-MethyltransferasesRetinoidsTransglutaminases

Identifiers

PMID15964820
PMCPMC1156990
OpenAlexW2122563784

What OpenQuestion holds

Textmetadata
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.