Evidence map›Paper›PMID 25779641›Full record

ArticleBiochimica et biophysica acta2015

C/EBPβ (CEBPB) protein binding to the C/EBP|CRE DNA 8-mer TTGC|GTCA is inhibited by 5hmC and enhanced by 5mC, 5fC, and 5caC in the CG dinucleotide.

Syed Khund Sayeed, Jianfei Zhao, Bangalore K Sathyanarayana, Jaya Prakash Golla, Charles Vinson

Open access · greenAbstract read
In one paragraph

Article in Biochimica et biophysica acta, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

31 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. SilencingEnvironmental epigenetics · 2025
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  11. Review
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  16. The bZIP mutant CEBPB (V285A) has sequence specific DNA binding propensities similar to CREB1.Biochimica et biophysica acta. Gene regulatory mechanisms · 2019
    Article
  17. Article
  18. Detecting and interpreting DNA methylation marks.Current opinion in structural biology · 2018
    Review
  19. Article
  20. 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

5 authors at 2 institutions in 1 country.

Syed Khund SayeedLaboratory of Metabolism, National Cancer Institute, National Institutes of Health, Room 3128, Building 37, Bethesda, MD 20892, United States.
Jianfei ZhaoLaboratory of Metabolism, National Cancer Institute, National Institutes of Health, Room 3128, Building 37, Bethesda, MD 20892, United States.
Bangalore K SathyanarayanaLaboratory of Molecular Biology, National Cancer Institute, National Institutes of Health, Room 5120, Building 37, Bethesda, MD 20892, United States.
Jaya Prakash GollaLaboratory of Metabolism, National Cancer Institute, National Institutes of Health, Room 3128, Building 37, Bethesda, MD 20892, United States.
Charles VinsonLaboratory of Metabolism, National Cancer Institute, National Institutes of Health, Room 3128, Building 37, Bethesda, MD 20892, United States. Electronic address: vinsonc@mail.nih.gov.
National Cancer Institute · USNational Institutes of Health · US

Funding

Gene Regulation and Function: The B-ZIP ProteinsZIABC005271 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI VINSON, CHARLES · 2009 to 2019
$11.2M
GENE REGULATION AND FUNCTION: THE B-ZIP PROTEINSZ01BC005271 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI VINSON, CHARLES · 1996 to 2008
$2.0M
Intramural NIH HHS Z01 BC005271
6 · The paper itself

Abstract

During mammalian development, some methylated cytosines (5mC) in CG dinucleotides are iteratively oxidized by TET dioxygenases to 5-hydroxymethylcytosine (5hmC), 5-formylcytosine (5fC), and 5-carboxylcytosine (5caC). The effect of these cytosine oxidative products on the sequence-specific DNA binding of transcription factors is being actively investigated. Here, we used the electrophoretic mobility shift assay (EMSA) to examine C/EBPα and C/EBPβ homodimers binding to all 25 chemical forms of a CG dinucleotide for two DNA sequences: the canonical C/EBP 8-mer TTGC|GCAA and the chimeric C/EBP|CRE 8-mer TTGC|GTCA. 5hmC in the CG dinucleotide in the C/EBP|CRE motif 8-mer TGAC|GCAA inhibits binding of C/EBPβ but not C/EBPα. Binding was increased by 5mC, 5fC and 5caC. Circular dichroism monitored thermal denaturations for C/EBPβ bound to the C/EBP|CRE motif confirmed the EMSA. The structural differences between C/EBPα and C/EBPβ that may account for the difference in binding 5hmC in the 8-mer TGAC|GCAA are explored.

Indexed as

5-MethylcytosineAnimalsCCAAT-Enhancer-Binding Protein-betaCCAAT-Enhancer-Binding ProteinsCrystallography, X-RayCytosineCytosine NucleotidesDNADNA-Binding ProteinsDNA MethylationEmbryonic DevelopmentNucleotide MotifsTranscription Factors5-carboxylcytosine5-formylcytosine5-hydroxymethylcytosine5-MethylcytosineCCAAT-Enhancer-Binding Protein-betaCCAAT-Enhancer-Binding ProteinsCEBPA protein, mouseCebpb protein, mouseCytosineCytosine NucleotidesDNADNA-Binding ProteinsTranscription Factors5hmC, 5fC, 5caC, carboxylation5mCBasic-leucine zipperC/EBP|CRE motifC/EBPβ homodimerCG dinucleotideDNA binding

Identifiers

PMID25779641
PMCPMC7857639
OpenAlexW2001689402

What OpenQuestion holds

Textmetadata
LicenceTDM
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.