Evidence map›Paper›PMID 39676670›Full record

ArticleNucleic acids research2025

ZNF143 binds DNA and stimulates transcription initiation to activate and repress direct target genes.

Jinhong Dong, Kizhakke Mattada Sathyan, Thomas G Scott, Rudradeep Mukherjee, Michael J Guertin

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Article in Nucleic acids research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

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0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Jinhong DongCenter for Cell Analysis and Modeling, University of Connecticut, 400 Farmington Ave, Farmington, Connecticut 06030, USA.
Kizhakke Mattada SathyanCenter for Cell Analysis and Modeling, University of Connecticut, 400 Farmington Ave, Farmington, Connecticut 06030, USA.ORCID 0000-0001-6469-7052
Thomas G ScottDepartment of Biochemistry and Molecular Genetics, University of Virginia, 1340 Jefferson Park Ave, Charlottesville, Virginia 22903, USA.
Rudradeep MukherjeeCenter for Cell Analysis and Modeling, University of Connecticut, 400 Farmington Ave, Farmington, Connecticut 06030, USA.
Michael J GuertinCenter for Cell Analysis and Modeling, University of Connecticut, 400 Farmington Ave, Farmington, Connecticut 06030, USA.ORCID 0000-0001-7148-3538

Funding

Mechanisms of coordinate gene regulation by transcription factorsR35GM128635 · NIGMS · UNIVERSITY OF VIRGINIA · PI Michael Joseph Guertin · 2018 to 2026
$3.4M
CSR NIH HHS R35-GM128635NIGMS NIH HHS R35 GM128635
6 · The paper itself

Abstract

Transcription factors bind to sequence motifs and act as activators or repressors. Transcription factors interface with a constellation of accessory cofactors to regulate distinct mechanistic steps to regulate transcription. We rapidly degraded the essential and pervasively expressed transcription factor ZNF143 to determine its function in the transcription cycle. ZNF143 facilitates RNA polymerase initiation and activates gene expression. ZNF143 binds the promoter of nearly all its activated target genes. ZNF143 also binds near the site of genic transcription initiation to directly repress a subset of genes. Although ZNF143 stimulates initiation at ZNF143-repressed genes (i.e. those that increase transcription upon ZNF143 depletion), the molecular context of binding leads to cis repression. ZNF143 competes with other more efficient activators for promoter access, physically occludes transcription initiation sites and promoter-proximal sequence elements, and acts as a molecular roadblock to RNA polymerases during early elongation. The term context specific is often invoked to describe transcription factors that have both activation and repression functions. We define the context and molecular mechanisms of ZNF143-mediated cis activation and repression.

Indexed as

DNAGene Expression RegulationTrans-ActivatorsTranscriptional ActivationTranscription Initiation, GeneticBinding SitesDNA-Directed RNA PolymerasesHumansPromoter Regions, GeneticProtein BindingTranscription FactorsTranscription, GeneticDNADNA-Directed RNA PolymerasesTrans-ActivatorsTranscription FactorsZNF143 protein, human

Identifiers

PMID39676670
PMCPMC11754675

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LicenceCC BY-NC
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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.