Evidence map›Paper›PMID 1569959›Full record

ArticleMolecular and cellular biology1992

Expression cloning of a novel zinc finger protein that binds to the c-fos serum response element.

R M Attar, M Z Gilman

Open access · greenAbstract readComparative Study
In one paragraph

Article in Molecular and cellular biology, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. A ligand-reversible dimerization system for controlling protein-protein interactions.Proceedings of the National Academy of Sciences of the United States of America · 2000
    Article
  6. Article
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  8. A general strategy to enhance the potency of chimeric transcriptional activators.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  9. Persistent increased DNA-binding and expression of serum response factor occur with epilepsy-associated long-term plasticity changes.The Journal of neuroscience : the official journal of the Society for Neuroscience · 1999
    Article
  10. The presence of transcription factors in chicken albumin, yolk and blastoderm.In vitro cellular & developmental biology. Animal · 1999
    Article
  11. The presence of transcription factors in fetal bovine sera.In vitro cellular & developmental biology. Animal · 1998
    Article
  12. Article
  13. A versatile synthetic dimerizer for the regulation of protein-protein interactions.Proceedings of the National Academy of Sciences of the United States of America · 1997
    Article
  14. Article
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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.

R M AttarCold Spring Harbor Laboratory, New York 11724.
M Z Gilman
Cold Spring Harbor Laboratory · US

Funding

MOLECULAR BIOLOGY OF CELLULAR TRANSFORMATIONP01CA046370 · NCI · COLD SPRING HARBOR LABORATORY · PI WIGLER, MICHAEL H · 1988 to 1992
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INDUCTION OF C-FOS EXPRESSION BY EXTRACELLULAR SIGNALSR01CA045642 · NCI · COLD SPRING HARBOR LABORATORY · PI GILMAN, MICHAEL Z · 1987 to 1996
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NCI NIH HHS CA45642NCI NIH HHS CA46370
6 · The paper itself

Abstract

Induction of c-fos transcription by serum growth factors requires the serum response element (SRE). The SRE is a multifunctional element which responds to several positively and negatively acting signals. To identify cellular proteins that might mediate functions of the SRE, we screened a human cDNA expression library with an SRE probe. We report the isolation and characterization of SRE-ZBP, a previously unidentified SRE-binding protein. SRE-ZBP is a member of the C2H2 zinc finger family of proteins exemplified by TFIIIA and the Drosophila Krüppel protein. The seven tandemly repeated zinc finger motifs in SRE-ZBP are sufficient for high-affinity binding to the SRE. We show that SRE-ZBP is a nuclear protein and identify a candidate cellular protein encoded by the SRE-ZBP gene. Because we cannot detect any DNA-binding activity attributable to the endogenous protein, we propose that SRE-ZBP activity may be subject to posttranslational regulation. Like c-fos mRNA, SRE-ZBP mRNA is serum inducible in HeLa cells, but with slower kinetics. The role of SRE-ZBP in the regulation of c-fos transcription remains unestablished, but this protein binds to a region of the SRE where mutations lead to derepression.

Indexed as

Genes, fosAmino Acid SequenceAnimalsBase Sequencebeta-GalactosidaseCloning, MolecularDNADNA-Binding ProteinsDNA ProbesEscherichia coliFluorescent Antibody TechniqueGene LibraryHumansImmune SeraMolecular Sequence DataNuclear Proteinsbeta-GalactosidaseDNADNA-Binding ProteinsDNA ProbesImmune SeraNuclear ProteinsOligodeoxyribonucleotidesRecombinant Fusion ProteinsSerum Response FactorTranscription Factors

Identifiers

PMID1569959
PMCPMC364416
OpenAlexW1882027619

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.