Evidence map›Paper›PMID 21106524›Full record

ArticleThe Journal of biological chemistry2011

PTB-associated splicing factor (PSF) functions as a repressor of STAT6-mediated Ig epsilon gene transcription by recruitment of HDAC1.

Lijie Dong, Xinyu Zhang, Xiao Fu, Xianzhi Zhang, Xingjie Gao, Mengyu Zhu, Xinting Wang, ZhenXia Yang, Ole Nørregaard Jensen, Juha Saarikettu and 3 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

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  16. PSF: nuclear busy-body or nuclear facilitator?Wiley interdisciplinary reviews. RNA
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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

13 authors at 3 institutions in 4 countries.

Lijie DongDepartment of Immunology, Basic Medical College, Tianjin Medical University, Heping District, Qixiangtai Road No. 22, Tianjin 300070, China.
Xinyu Zhang
Xiao Fu
Xianzhi Zhang
Xingjie Gao
Mengyu Zhu
Xinting Wang
ZhenXia Yang
Ole Nørregaard Jensen
Juha Saarikettu
Zhi Yao
Olli Silvennoinen
Jie Yang
Ministry of Education of the People's Republic of China · CNTampere University Hospital · FIUniversity of Southern Denmark · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regulation of transcription requires cooperation between sequence-specific transcription factors and numerous coregulatory proteins. In IL-4/IL-13 signaling several coactivators for STAT6 have been identified, but the molecular mechanisms of STAT6-mediated gene transcription are still not fully understood. Here we identified by proteomic approach that the PTB-associated splicing factor (PSF) interacts with STAT6. In intact cells the interaction was observed only after IL-4 stimulation. The IL-4-induced tyrosine phosphorylation of both STAT6 and PSF is a prerequisite for the efficient association of the two proteins. Functional analysis demonstrated that ectopic expression of PSF resulted in inhibition of STAT6-mediated transcriptional activation and mRNA expression of the Igε germline heavy chain gene, whereas knockdown of PSF increased the STAT6-mediated responses. PSF recruited histone deacetylase 1 (HDAC1) to the STAT6 transcription complex, which resulted in reduction of H3 acetylation at the promoter regions of Ig heavy chain germline Igε and inhibition of STAT6-mediated transcription. In addition, the HDACs inhibitor trichostatin A (TSA) enhanced H3 acetylation, and reverted the PSF-mediated transcriptional repression of Igε gene transcription. In summary, these results identify PSF as a repressor of STAT6-mediated transcription that functions through recruitment of HDAC to the STAT6 transcription complex, and delineates a novel regulatory mechanism of IL-4 signaling that may have implications in the pathogenesis of allergic diseases and pharmacological HDAC inhibition in lymphomas.

Indexed as

Transcription, GeneticGenes, ImmunoglobulinHeLa CellsHistone Deacetylase 1HumansImmunoglobulin epsilon-ChainsInterleukin-4Protein BindingProtein Interaction MappingProtein TransportPTB-Associated Splicing FactorRepressor ProteinsRNA-Binding ProteinsSTAT6 Transcription FactorTranscriptional ActivationHistone Deacetylase 1Immunoglobulin epsilon-ChainsInterleukin-4PTB-Associated Splicing FactorRepressor ProteinsRNA-Binding ProteinsSTAT6 protein, humanSTAT6 Transcription Factor

Identifiers

PMID21106524
PMCPMC3030351
OpenAlexW2078234461

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.