Evidence map›Paper›PMID 18458062›Full record

ArticleMolecular and cellular biology2008

Zinc-induced formation of a coactivator complex containing the zinc-sensing transcription factor MTF-1, p300/CBP, and Sp1.

Yong Li, Tomoki Kimura, Ryan W Huyck, John H Laity, Glen K Andrews

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

33 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
  2. Review
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  7. CpG Site-Specific Regulation of Metallothionein-1 Gene Expression.International journal of molecular sciences · 2020
    Article
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  10. The Irving-Williams series and the 2-His-1-carboxylate facial triad: a thermodynamic study of MnJournal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2018
    Article
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  13. Review
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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

5 authors at 2 institutions in 1 country.

Yong LiDepartment of Biochemistry and Molecular Biology, Mail Stop 3030, University of Kansas Medical Center, 39th and Rainbow Blvd., Kansas City, KS 66160-7421, USA.
Tomoki Kimura
Ryan W Huyck
John H Laity
Glen K Andrews
University of Kansas Medical Center · USUniversity of Missouri–Kansas City · US

Funding

ENVIRONMENTAL TOXICOLOGY USING TRANSGENIC MOUSE MODELSR01ES005704 · NIEHS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI ANDREWS, GLEN K · 1991 to 2005
$2.0M
Mechanisms of Eukaryotic Zinc HomeostasisR01GM073771 · NIGMS · UNIVERSITY OF MISSOURI KANSAS CITY · PI LAITY, JOHN HAROLD · 2007 to 2011
$1.5M
NIEHS NIH HHS ES05704NIEHS NIH HHS R01 ES005704NIGMS NIH HHS GM073771NIGMS NIH HHS R01 GM073771
6 · The paper itself

Abstract

Herein, the mechanisms of transactivation of gene expression by mouse metal response element-binding transcription factor 1 (MTF-1) were investigated. Evidence obtained from coimmunoprecipitation assays revealed that exposure of the cells to zinc resulted in the rapid formation of a multiprotein complex containing MTF-1, the histone acetyltransferase p300/CBP, and the transcription factor Sp1. Down-regulation of endogenous p300 expression by small interfering RNA transfection significantly decreased zinc-dependent metallothionein I (MT-I) gene transcription without altering induction of zinc transporter 1 (ZnT1). MTF-1 independently facilitated the recruitment of Sp1 and p300 to the protein complex in response to zinc. Mutagenesis demonstrated that the acidic domain, one of three transactivation domains of MTF-1, is required for recruitment of p300 but not Sp1 as well as for zinc-dependent activation of MT-I gene transcription. Furthermore, mutation of leucine residues (L-->A) within a nuclear exclusion signal in the MTF-1 acidic domain impaired recruitment of p300 and zinc-dependent activation of the MT-I gene. Nuclear magnetic resonance characterization of an isolated protein fragment corresponding to the MTF-1 acidic region demonstrated that this region is largely unstructured in the presence and absence of excess stoichiometric amounts of zinc. This suggests that the mechanism by which MTF-1 recruits p300 to this complex involves extrinsic-zinc-dependent steps. These studies reveal a novel zinc-responsive mechanism requiring an acidic region of MTF-1 that functions as a nuclear exclusion signal as well as participating in formation of a coactivator complex essential for transactivation of MT-I gene expression.

Indexed as

AnimalsCadmiumDNA-Binding ProteinsImmunoprecipitationLeucineMetallothioneinMicep300-CBP Transcription FactorsProtein BindingProtein Structure, SecondaryProtein Structure, TertiaryRNA, Small InterferingSequence DeletionSp1 Transcription FactorTime FactorsTranscriptional ActivationCadmiumDNA-Binding ProteinsLeucineMetallothioneinp300-CBP Transcription FactorsRNA, Small InterferingSp1 Transcription FactorTranscription Factor MTF-1Transcription FactorsZinc

Identifiers

PMID18458062
PMCPMC2447150
OpenAlexW2111548566

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.