Evidence map›Paper›PMID 19952285›Full record

ArticleMolecular endocrinology (Baltimore, Md.)2010

Long-range transcriptional control of progesterone receptor gene expression.

Jamie Bonéy-Montoya, Yvonne S Ziegler, Carol D Curtis, Jonathan A Montoya, Ann M Nardulli

Open access · bronzeAbstract read
In one paragraph

Article in Molecular endocrinology (Baltimore, Md.), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

32 citing papers in PubMed, 54 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Allopregnanolone: Metabolism, Mechanisms of Action, and Its Role in Cancer.International journal of molecular sciences · 2022
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Expression of estrogen receptor α in the mouse cerebral cortex.Molecular and cellular endocrinology · 2015
    Article
  16. Increased association between endometriosis and endometrial cancer: a nationwide population-based retrospective cohort study.International journal of gynecological cancer : official journal of the International Gynecological Cancer Society · 2015
    Article
  17. Article
  18. Article
  19. Article
  20. 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

5 authors at 2 institutions in 1 country.

Jamie Bonéy-MontoyaDepartment of Molecular and Integrative Physiology, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA.
Yvonne S Ziegler
Carol D Curtis
Jonathan A Montoya
Ann M Nardulli
Urbana University · USUniversity of Illinois Urbana-Champaign · US

Funding

Cellular and Molecular Biology Training GrantT32GM007283 · NIGMS · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI MORRISSEY, JAMES H. · 1985 to 2011
$4.7M
INTERACTION OF THE ESTROGEN RECEPTOR WITH DNAR01DK053884 · NIDDK · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI NARDULLI, ANN · 1999 to 2014
$4.0M
Regulation of Estrogen-Responsive GenesR01DK061463 · NIDDK · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI NARDULLI, ANN · 2004 to 2007
$1.3M
Interaction of the Estrogen Receptor with DNAR56DK053884 · NIDDK · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI NARDULLI, ANN · 2008 to 2008
$269k
NIDDK NIH HHS DK 0601463NIDDK NIH HHS DK53884NIDDK NIH HHS R01 DK053884NIDDK NIH HHS R01 DK061463NIDDK NIH HHS R56 DK053884NIGMS NIH HHS 5T32GM007283NIGMS NIH HHS T32 GM007283
6 · The paper itself

Abstract

Estrogen receptor alpha (ERalpha) binds to specific target DNA sequences, estrogen response elements (EREs), to regulate estrogen-responsive gene expression. The progesterone receptor (PR) gene has been used extensively as a marker of estrogen responsiveness. Although we previously identified cis elements within 1 kb of the PR-B transcription start site that are associated with ERalpha and help to confer estrogen responsiveness, the identification of ERalpha binding sites far removed from the transcription start site suggested that long-range regulation of this gene may occur. We now show that eight regions of the PR gene from 311 kb upstream to 4 kb downstream of the PR-B transcription start site interact with ERalpha and that coactivator proteins and acetylated histones are selectively associated with these gene regions. Specific PR gene regions confer estrogen responsiveness to a heterologous reporter plasmid, and mutation of EREs within these regions diminishes estrogen-induced transactivation. Importantly, chromosome conformation capture assays reveal ERalpha- and ligand-dependent interactions between proximal and distal PR gene regions. Taken together, our studies suggest that distal regions of the PR gene participate in the dynamic regulation of this gene and that the coordinated action of proximal and distal PR gene regions allows cells to respond to changes in hormone levels with extraordinary versatility and sensitivity.

Indexed as

Gene Expression RegulationAcetylationCell Line, TumorChromatinComputational BiologyDNA-Binding ProteinsEstradiolEstrogen Receptor alphaEstrogensForkhead Transcription FactorsHistonesHumansNuclear Receptor Coactivator 3Nucleic Acid Conformationp300-CBP-Associated Factorp300-CBP Transcription FactorsChromatinDNA-Binding ProteinsEstradiolEstrogen Receptor alphaEstrogensForkhead Transcription FactorsFOXF2 protein, humanHistonesNCOA3 protein, humanNuclear Receptor Coactivator 3p300-CBP-Associated Factorp300-CBP Transcription FactorsReceptors, ProgesteroneRNA, MessengerTRPC6 Cation ChannelTRPC6 protein, humanTRPC Cation Channels

Identifiers

PMID19952285
PMCPMC2817601
OpenAlexW2003758571

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.