Evidence map›Paper›PMID 19906647›Full record

ArticleThe Journal of biological chemistry2010

Epigenetic mechanisms modulate thyroid transcription factor 1-mediated transcription of the surfactant protein B gene.

Yuxia Cao, Tiffany Vo, Guetchyn Millien, Jean-Bosco Tagne, Darrell Kotton, Robert J Mason, Mary C Williams, Maria I Ramirez

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

25 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
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  8. The epigenetic basis of cellular plasticity.Current opinion in cell biology · 2017
    Review
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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

8 authors at 2 institutions in 1 country.

Yuxia CaoPulmonary Center, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts 02118, USA. yxcao@bu.edu
Tiffany Vo
Guetchyn Millien
Jean-Bosco Tagne
Darrell Kotton
Robert J Mason
Mary C Williams
Maria I Ramirez
Boston University · USUniversity of Colorado Denver · US

Funding

T1alpha in type I cell formation, regulation &functionP01HL047049 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI LU, JINING · 1992 to 2012
$27.6M
FUNCTIONS OF PULMONARY ALVEOLARY TYPE II CELLS IN VITROR01HL029891 · NHLBI · NATIONAL JEWISH HEALTH · PI MASON, ROBERT JAMES · 1985 to 2009
$2.9M
FUNCTIONS OF PULMONARY ALVEOLAR TYPE II CELLS IN VITROR37HL029891 · NHLBI · NATIONAL JEWISH HEALTH · PI MASON, ROBERT JAMES · 1991 to 2000
$305k
NHLBI NIH HHS HL 029891NHLBI NIH HHS P01 HL047049NHLBI NIH HHS R01 HL029891NHLBI NIH HHS R37 HL029891
6 · The paper itself

Abstract

Epigenetic regulation of transcription plays an important role in cell-specific gene expression by altering chromatin structure and access of transcriptional regulators to DNA binding sites. Surfactant protein B (Sftpb) is a developmentally regulated lung epithelial gene critical for lung function. Thyroid transcription factor 1 (Nkx2-1) regulates Sftpb gene expression in various species. We show that Nkx2-1 binds to the mouse Sftpb (mSftpb) promoter in the lung. In a mouse lung epithelial cell line (MLE-15), Nkx2-1 knockdown reduces Sftpb expression, and mutation of Nkx2-1 cis-elements significantly reduces mSftpb promoter activity. Whether chromatin structure modulates Nkx2-1 regulation of Sftpb transcription is unknown. We found that DNA methylation of the mSftpb promoter inversely correlates with known patterns of Sftpb expression in vivo. The mSftpb promoter activity can be manipulated by altering its cytosine methylation status in vitro. Nkx2-1 activation of the mSftpb promoter is impaired by DNA methylation. The unmethylated Sftpb promoter shows an active chromatin structure enriched in the histone modification H3K4me3 (histone 3-lysine 4 trimethylated). The ATP-dependent chromatin remodeling protein Brg1 is recruited to the Sftpb promoter in Sftpb-expressing, but not in non-expressing tissues and cell lines. Brg1 knockdown in MLE-15 cells greatly decreases H3K4me3 levels at the Sftpb promoter region and expression of the Sftpb gene. Brg1 can be co-immunoprecipitated with Nkx2-1 protein. Last, Nkx2-1 and Brg1 with intact ATPase activity are required for mSftpb promoter activation in vitro. Our findings suggest that DNA methylation and chromatin modifications cooperate with Nkx2-1 to regulate Sftpb gene cell specific expression.

Indexed as

Epigenesis, GeneticTranscription, GeneticAdenosine TriphosphatasesAnimalsAzacitidineCell LineChromatinCpG IslandsDecitabineDNA HelicasesDNA MethylationEpithelial CellsFemaleHumansLungMaleAdenosine TriphosphatasesAzacitidineChromatinDecitabineDNA HelicasesNKX2-1 protein, humanNkx2-1 protein, mouseNkx2-1 protein, ratNuclear ProteinsPulmonary Surfactant-Associated Protein BSMARCA4 protein, humanThyroid Nuclear Factor 1Transcription Factors

Identifiers

PMID19906647
PMCPMC2804371
OpenAlexW2090695673

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.