Evidence map›Paper›PMID 14627821›Full record

ArticleNucleic acids research2003

Chromatin acetylation and remodeling at the Cis promoter during STAT5-induced transcription.

Anne Rascle, Emma Lees

Open access · bronzeAbstract read
In one paragraph

Article in Nucleic acids research, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

20 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
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  13. CIS: the late-blooming eldest son.Nature immunology · 2013
    Article
  14. Article
  15. Article
  16. p65 Negatively regulates transcription of the cyclin E gene.The Journal of biological chemistry · 2010
    Article
  17. Article
  18. Article
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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

2 authors.

Anne RascleDepartment of Discovery Research, DNAX Research Inc., 901 California Avenue, Palo Alto, CA 94304, USA.
Emma Lees

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The signal transducer and activator of transcription STAT5 plays a major role in cytokine-induced expression of genes involved in cell proliferation and survival. Although several STAT5 partners have been identified, the molecular events taking place at the promoter level upon STAT5 recruitment have not yet been characterized in great detail. Using chromatin immunoprecipitation and accessibility assays, we characterized histone acetylation and chromatin remodeling events occurring during transcriptional activation of the endogenous murine Cis gene, a STAT5 target gene, in response to IL-3. We found that STAT5 binding in vivo is associated with low histone H3 and H4 acetylation levels in the proximity of the STAT5 binding sites. STAT5 recruitment also results in chromatin reorganization over that promoter region. These events (STAT5 binding, histone acetylation and chromatin remodeling) are not sufficient for transcriptional activation, which requires a non-histone protein deacetylase. These data reveal novel implications of STAT5 in chromatin regulation during cytokine-induced transcription, thus contributing to a better understanding of the mechanism of transcriptional activation by STAT5.

Indexed as

Milk ProteinsTranscriptional ActivationTranscription, GeneticAcetylationAnimalsBinding SitesB-LymphocytesCell LineChromatinDNA-Binding ProteinsImmediate-Early ProteinsInterleukin-3MicePrecipitin TestsPromoter Regions, GeneticProtein BindingChromatinDNA-Binding ProteinsImmediate-Early ProteinsInterleukin-3Milk ProteinsProto-Oncogene Proteins c-fosStat5a protein, mouseSTAT5 Transcription FactorSuppressor of Cytokine Signaling ProteinsTrans-Activators

Identifiers

PMID14627821
PMCPMC290274
OpenAlexW2162384201

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.