Evidence map›Paper›PMID 12665568›Full record

ArticleMolecular and cellular biology2003

Antithetic effects of MBD2a on gene regulation.

Hidetoshi Fujita, Ryouji Fujii, Satoko Aratani, Tetsuya Amano, Akiyoshi Fukamizu, Toshihiro Nakajima

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

23 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. The methylated-DNA binding protein MBD2 enhances NGFI-A (egr-1)-mediated transcriptional activation of the glucocorticoid receptor.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2014
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. The implications of DNA methylation for toxicology: toward toxicomethylomics, the toxicology of DNA methylation.Toxicological sciences : an official journal of the Society of Toxicology · 2011
    Article
  17. Article
  18. Article
  19. Article
  20. Epigenetic programming of the rRNA promoter by MBD3.Molecular and cellular biology · 2007
    Article
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 4 institutions in 2 countries.

Hidetoshi FujitaInstitute of Medical Science, St. Marianna University School of Medicine, Miyamae-ku, Kawasaki, Kanagawa 216-8512, Japan.
Ryouji Fujii
Satoko Aratani
Tetsuya Amano
Akiyoshi Fukamizu
Toshihiro Nakajima
St. Marianna University School of Medicine · JPAlliance University · INInstitute of Applied Biochemistry · JPUniversity of Tsukuba · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA methylation is essential for epigenetic gene regulation during development. The cyclic AMP (cAMP)-responsive element (CRE) is found in the promoter of many cAMP-regulated genes and plays important roles in their gene expression. Methylation occurs on the CRE site and results in transcriptional repression via a direct mechanism, that is, prevention by the methyl group of binding of the cAMP-responsive factor CREB to this site. A recent study indicated that the nucleosome is also important in repressing transcription. In this study, we investigated the regulation of transcriptional repression on methylated CRE. We focused on methyl-CpG binding domain protein 2 (MBD2). MBD2 consists of two forms, MBD2a and MBD2b, the latter lacking the N-terminal extension of MBD2a. Unexpectedly, we found that MBD2a, but not MBD2b, promoted activation of the unmethylated cAMP-responsive genes. An in vivo binding assay revealed that MBD2a selectively interacted with RNA helicase A (RHA), a component of CREB transcriptional coactivator complexes. MBD2a and RHA cooperatively enhanced CREB-dependent gene expression. Interestingly, coimmunoprecipitation assays demonstrated that MBD2a binding to RHA was not associated with histone deacetylase 1. Our results indicate a novel role for MBD2a in gene regulation.

Indexed as

DNA MethylationGene Expression RegulationAutoantigensBase SequenceBinding SitesCell LineCyclic AMPCyclic AMP Response Element-Binding ProteinDEAD-box RNA HelicasesDNADNA-Binding ProteinsHistone Deacetylase 1Histone DeacetylasesHumansModels, BiologicalNeoplasm ProteinsAutoantigensCyclic AMPCyclic AMP Response Element-Binding ProteinDEAD-box RNA HelicasesDHX9 protein, humanDNADNA-Binding ProteinsHDAC1 protein, humanHistone Deacetylase 1Histone DeacetylasesMBD2 proteinNeoplasm ProteinsRecombinant ProteinsRNA Helicases

Identifiers

PMID12665568
PMCPMC152551
OpenAlexW2166332466

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.