Evidence map›Paper›PMID 18653526›Full record

ArticleNucleic acids research2008

Chromatin profiling across the human tumour necrosis factor gene locus reveals a complex, cell type-specific landscape with novel regulatory elements.

Jennifer M Taylor, Kate Wicks, Claire Vandiedonck, Julian C Knight

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

  1. Role of PRDM1 in natural killer cells.Molecular biology reports · 2026
    Review
  2. Article
  3. Journal of immunology research · 2022
    Article
  4. Article
  5. Article
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  10. Review
  11. Article
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  14. Article
  15. PRDM1/Blimp-1 controls effector cytokine production in human NK cells.Journal of immunology (Baltimore, Md. : 1950) · 2010
    Article
  16. Transcriptional control of the TNF gene.Current directions in autoimmunity · 2010
    Review
  17. The human Major Histocompatibility Complex as a paradigm in genomics research.Briefings in functional genomics & proteomics · 2009
    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

4 authors at 2 institutions in 1 country.

Jennifer M TaylorWellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK.
Kate Wicks
Claire Vandiedonck
Julian C Knight
University of Oxford · GBCentre for Human Genetics · GB

Funding

Wellcome Trust 074318Wellcome Trust 074318/Z/04/Z
6 · The paper itself

Abstract

The TNF locus on chromosome 6p21 encodes a family of proteins with key roles in the immune response whose dysregulation leads to severe disease. Transcriptional regulation is important, with cell type and stimulus-specific enhancer complexes involving the proximal TNF promoter. We show how quantitative chromatin profiling across a 34 kb region spanning the TNF locus has allowed us to identify a number of novel DNase hypersensitive sites and characterize more distant regulatory elements. We demonstrate DNase hypersensitive sites corresponding to the lymphotoxin alpha (LTA) and tumour necrosis factor (TNF) promoter regions, a CpG island in exon 4 of lymphotoxin beta (LTB), the 3' end of nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor-like 1 (NFKBIL1) and 3.4 kb upstream of LTA. These sites co-localize to highly conserved DNA sequences and show evidence of cell type specificity when lymphoblastoid, Jurkat, U937, HeLa and HEK293T cell lines are analysed using Southern blotting. For Jurkat T cells, we define histone modifications across the locus. Peaks of acetylated histone H3 and H4, together with tri-methyl K4 of histone H3, correspond to hypersensitive sites, notably in exon 4 of LTB. We provide evidence of a functional role for an intergenic DNase I hypersensitive site distal to LTA in Jurkat cells based on reporter gene analysis, with evidence of recruitment of upstream stimulatory factors (USF) transcription factors.

Indexed as

Regulatory Elements, TranscriptionalBase SequenceBlotting, SouthernCell LineChromatinConserved SequenceDeoxyribonuclease IDNA FootprintingEnhancer Elements, GeneticHistonesHumansJurkat CellsLymphotoxin-alphaPhylogenyTumor Necrosis FactorsChromatinDeoxyribonuclease IHistonesLymphotoxin-alphaTumor Necrosis Factors

Identifiers

PMID18653526
PMCPMC2528168
OpenAlexW2136853376

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.