Evidence map›Paper›PMID 15964799›Full record

ArticleMolecular and cellular biology2005

Differential regulation of estrogen-inducible proteolysis and transcription by the estrogen receptor alpha N terminus.

Christopher C Valley, Raphaël Métivier, Natalia M Solodin, Amy M Fowler, Mara T Mashek, Lindsay Hill, Elaine T Alarid

Abstract read
In one paragraph

Article in Molecular and cellular biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
4.0field-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

59 citing papers in PubMed, 103 citations in OpenAlex.

  1. Defining the DNA Binding Specificity of GRHL2.bioRxiv : the preprint server for biology · 2026
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  9. Forskolin Stimulates Estrogen Receptor (ER)International journal of endocrinology · 2022
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  10. Review
  11. CDK7 inhibitors as anticancer drugs.Cancer metastasis reviews · 2020
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  14. Grainyhead-like 2 as a double-edged sword in development and cancer.American journal of translational research · 2020
    Review
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  18. Review
  19. Article
  20. Expression of CDK7, Cyclin H, and MAT1 Is Elevated in Breast Cancer and Is Prognostic in Estrogen Receptor-Positive Breast Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2016
    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

7 authors at 2 institutions in 2 countries.

Christopher C ValleyDepartment of Physiology, 1300 University Ave., 120 SMI, University of Wisconsin--Madison, Madison, Wisconsin 53706, USA.
Raphaël Métivier
Natalia M Solodin
Amy M Fowler
Mara T Mashek
Lindsay Hill
Elaine T Alarid
University of Wisconsin–Madison · USUniversité de Rennes · FR

Funding

Proteolytic Regulation of Estrogen Receptor-alphaR01DK064034 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI ALARID, ELAINE T · 2004 to 2007
$819k
NIDDK NIH HHS DK64034NIDDK NIH HHS R01 DK064034
6 · The paper itself

Abstract

The ubiquitin-proteasome pathway has emerged as an important regulatory mechanism governing the activity of several transcription factors. While estrogen receptor alpha (ERalpha) is also subjected to rapid ubiquitin-proteasome degradation, the relationship between proteolysis and transcriptional regulation is incompletely understood. Based on studies primarily focusing on the C-terminal ligand-binding and AF-2 transactivation domains, an assembly of an active transcriptional complex has been proposed to signal ERalpha proteolysis that is in turn necessary for its transcriptional activity. Here, we investigated the role of other regions of ERalpha and identified S118 within the N-terminal AF-1 transactivation domain as an additional element for regulating estrogen-induced ubiquitination and degradation of ERalpha. Significantly, different S118 mutants revealed that degradation and transcriptional activity of ERalpha are mechanistically separable functions of ERalpha. We find that proteolysis of ERalpha correlates with the ability of ERalpha mutants to recruit specific ubiquitin ligases regardless of the recruitment of other transcription-related factors to endogenous model target genes. Thus, our findings indicate that the AF-1 domain performs a previously unrecognized and important role in controlling ligand-induced receptor degradation which permits the uncoupling of estrogen-regulated ERalpha proteolysis and transcription.

Indexed as

Gene Expression RegulationTranscription, GeneticAmino Acid SequenceCell LineChromatin ImmunoprecipitationEstradiolEstrogen AntagonistsEstrogen Receptor alphaEstrogensEthanolFulvestrantHumansHydrolysisKidneyLigandsPromoter Regions, GeneticEstradiolEstrogen AntagonistsEstrogen Receptor alphaEstrogensEthanolFulvestrantLigandsSerineUbiquitin

Identifiers

PMID15964799
PMCPMC1156995
OpenAlexW2150344507

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.