Evidence map›Paper›PMID 17636311›Full record

ArticleNucleic acids research2007

Interaction of estrogen receptor alpha with proliferating cell nuclear antigen.

Jennifer R Schultz-Norton, Vivian A Gabisi, Yvonne S Ziegler, Ian X McLeod, John R Yates, Ann M Nardulli

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2007. 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
2.2field-weighted citation impact, top 11% 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, 27 citations in OpenAlex.

  1. Article
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  7. Review
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  11. Article
  12. Article
  13. Isolation of proteins associated with the DNA-bound estrogen receptor alpha.Methods in molecular biology (Clifton, N.J.) · 2009
    Article
  14. Using RNA interference to study protein function.Methods in molecular biology (Clifton, N.J.) · 2009
    Article
  15. Article
  16. 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

6 authors at 2 institutions in 1 country.

Jennifer R Schultz-NortonDepartment of Molecular and Integrative Physiology, University of Illinois, Urbana, IL 61801, USA.
Vivian A Gabisi
Yvonne S Ziegler
Ian X McLeod
John R Yates
Ann M Nardulli
Scripps Research Institute · USUniversity of Illinois Urbana-Champaign · US

Funding

ZDS2P REGULATES SWE1P-DEPENDENT POLARIZED CELL GROWTH IN S CEREVISIAEP41RR011823 · NCRR · UNIVERSITY OF WASHINGTON · PI DAVIS, TRACY · 1996 to 2011
$24.7M
INTERACTION OF THE ESTROGEN RECEPTOR WITH DNAR01DK053884 · NIDDK · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI NARDULLI, ANN · 1999 to 2014
$4.0M
PROGRAM OF RESEARCH TRAINING IN REPRODUCTIVE BIOLOGYT32HD007028 · NICHD · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI MILLER, DAVID JOEL · 1985 to 2005
$1.4M
NCRR NIH HHS P41 RR011823NCRR NIH HHS P41 RR11823-10NICHD NIH HHS T32 HD007028NICHD NIH HHS T32 HD07028NIDDK NIH HHS R01 DK053884NIDDK NIH HHS R01 DK 53884
6 · The paper itself

Abstract

The ability of estrogen receptor alpha (ERalpha) to modulate gene expression is influenced by the recruitment of a host of co-regulatory proteins to target genes. To further understand how estrogen-responsive genes are regulated, we have isolated and identified proteins associated with ERalpha when it is bound to DNA containing the consensus estrogen response element (ERE). One of the proteins identified in this complex, proliferating cell nuclear antigen (PCNA), is required for DNA replication and repair. We show that PCNA interacts with ERalpha in the absence and in the presence of DNA, enhances the interaction of ERalpha with ERE-containing DNA, and associates with endogenous estrogen-responsive genes. Interestingly, rather than altering hormone responsiveness of endogenous, estrogen-responsive genes, PCNA increases the basal expression of these genes. Our studies suggest that in addition to serving as a platform for the recruitment of DNA replication and repair proteins, PCNA may serve as a platform for transcription factors involved in regulating gene expression.

Indexed as

Cell Line, TumorEstradiolEstrogen Receptor alphaHumansProliferating Cell Nuclear AntigenResponse ElementsTranscription, GeneticEstradiolEstrogen Receptor alphaProliferating Cell Nuclear Antigen

Identifiers

PMID17636311
PMCPMC1976446
OpenAlexW2096749315

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.