Evidence map›Paper›PMID 8755515›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1996

SMRT isoforms mediate repression and anti-repression of nuclear receptor heterodimers.

J D Chen, K Umesono, R M Evans

Open access · greenAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
13.0field-weighted citation impact, top 1% 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

76 citing papers in PubMed, 244 citations in OpenAlex.

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  11. Epigenetic distortion to VDR transcriptional regulation in prostate cancer cells.The Journal of steroid biochemistry and molecular biology · 2013
    Review
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16 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

J D ChenThe Salk Institute for Biological Studies, Howard Hughes Medical Institute, La Jolla, CA 92037, USA.
K Umesono
R M Evans
Nara Institute of Science and Technology · JP

Funding

SPATIAL REGULATION OF DEVELOPMENTAL GENE EXPRESSIONR01HD027183 · NICHD · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI EVANS, RONALD M · 1990 to 2009
$3.6M
HORMONAL REGULATION OF MAMMALIAN GENE EXPRESSIONR01GM026444 · NIGMS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI EVANS, RONALD M. · 1985 to 1989
–
HORMONAL REGULATION OF MAMMALIAN GENE EXPRESSIONR37GM026444 · NIGMS · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI EVANS, RONALD M. · 1990 to 1999
–
NICHD NIH HHS CHD27183NIGMS NIH HHS GM26444
6 · The paper itself

Abstract

Transcriptional repression represents an important component in the regulation of cell differentiation and oncogenesis mediated by nuclear hormone receptors. Hormones act to relieve repression, thus allowing receptors to function as transcriptional activators. The transcriptional corepressor SMRT was identified as a silencing mediator for retinoid and thyroid hormone receptors. SMRT is highly related to another corepressor, N-CoR, suggesting the existence of a new family of receptor-interacting proteins. We demonstrate that SMRT is a ubiquitous nuclear protein that interacts with unliganded receptor heterodimers in mammalian cells. Furthermore, expression of the receptor-interacting domain of SMRT acts as an antirepressor, suggesting the potential importance of splicing variants as modulators of thyroid hormone and retinoic acid signaling.

Indexed as

Saccharomyces cerevisiae ProteinsTranscription FactorsTranscription, GeneticAlternative SplicingAnimalsCell LineChlorocebus aethiopsDNA-Binding ProteinsFungal ProteinsGene Expression RegulationKidneyModels, StructuralNuclear ProteinsNuclear Receptor Co-Repressor 1Nuclear Receptor Co-Repressor 2Receptors, Cytoplasmic and NuclearDNA-Binding ProteinsFungal ProteinsGAL4 protein, S cerevisiaeNuclear ProteinsNuclear Receptor Co-Repressor 1Nuclear Receptor Co-Repressor 2Receptors, Cytoplasmic and NuclearRecombinant Fusion ProteinsRepressor ProteinsSaccharomyces cerevisiae ProteinsTranscription Factors

Identifiers

PMID8755515
PMCPMC38786
OpenAlexW2097724305

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.