Evidence map›Paper›PMID 18194566›Full record

ArticleBMC molecular biology2008

Regulation of mouse Scgb3a1 gene expression by NF-Y and association of CpG methylation with its tissue-specific expression.

Takeshi Tomita, Shioko Kimura

Open access · hybridAbstract read
In one paragraph

Article in BMC molecular biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 31% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Aberrant promoter methylation of HIN-1 gene may contribute to the pathogenesis of breast cancer: a meta-analysis.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Pooled it
  2. Article
  3. Article
  4. Article
  5. Hypothalamic food intake regulation in a cancer-cachectic mouse model.Journal of cachexia, sarcopenia and muscle · 2014
    Article
  6. Article
  7. Article
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  10. Oncostatin M regulates secretoglobin 3A1 and 3A2 expression in a bidirectional manner.American journal of respiratory cell and molecular biology · 2009
    Article
  11. 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

2 authors at 1 institution in 1 country.

Takeshi TomitaLaboratory of Metabolism, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA. tomitat@mail.nih.gov
Shioko Kimura
National Cancer Institute · US

Funding

Role of Novel Cytokine Secretoglobin (SCGB) 3A2 in LungZIABC010449 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KIMURA, SHIOKO · 2009 to 2025
$10.3M
Uteroglobin-Related Protein (UGRP) 1 in Lung InflammatioZ01BC010449 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI KIMURA, SHIOKO · 2002 to 2008
$594k
Intramural NIH HHS Z01 BC010449Intramural NIH HHS Z99 CA999999
6 · The paper itself

Abstract

backgroundSecretoglobin (SCGB) 3A1 is a secretory protein of small molecular weight with tumor suppressor function. It is highly expressed in lung and trachea in both human and mouse, with additional tissues expressing the protein that differ depending on the species. However, little is known about the function and transcriptional regulation of this gene in normal mouse tissues.

resultsBy reporter gene transfection and gel mobility shift analyses, we demonstrated that expression of the mouse Scgb3a1 gene is regulated by a PU-box binding protein and a ubiquitous transcription factor NF-Y that respectively binds to the PU-boxes located at -99 to -105 bp and -158 to -164 bp, and the "CCAAT" binding sites located at -425 to -429 bp and -498 to -502 bp from the transcription start site of the gene. However, the effect of PU-box binding protein on transcriptional activation is minimal as compared to NF-Y, suggesting that NF-Y is a more critical transcription factor for mouse Scgb3a1 gene transcription. Despite that NF-Y is a ubiquitous factor, Scgb3a1 is highly expressed only in mouse lung and mtCC cells that are derived from SV40 transformed mouse Clara cells, but not in ten other mouse tissues/cells examined. Gene methylation analysis revealed that within 600 bp of the Scgb3a1 gene promoter region, there are nine CpG methylation sites present, of which two CpGs closest to the transcription start site of the gene are unmethylated in the tissues/cells expressing SCGB3A1.

conclusionA ubiquitous transcription factor NF-Y binds to and activates expression of the mouse Scgb3a1 gene and tissue-specific expression of the gene is associated with CpG methylation of the promoter.

Indexed as

CpG IslandsDNA MethylationAnimalsBase SequenceBinding SitesCCAAT-Binding FactorCells, CulturedChlorocebus aethiopsCOS CellsDNADNA PrimersGene Expression RegulationGenes, ReporterLungMiceMolecular Sequence DataCCAAT-Binding FactorDNADNA PrimersProteinsProtein SubunitsRecombinant ProteinsUGRP2 protein, mouse

Identifiers

PMID18194566
PMCPMC2266941
OpenAlexW2012166422

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.