Evidence map›Paper›PMID 28864474›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2017

The Scaffolding Protein IQGAP1 Interacts with NLRC3 and Inhibits Type I IFN Production.

Aaron M Tocker, Emily Durocher, Kimberly D Jacob, Kate E Trieschman, Suzanna M Talento, Alma A Rechnitzer, David M Roberts, Beckley K Davis

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

18 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Single-cell analysis revealsScience advances · 2025
    Article
  6. Article
  7. The NLR gene family: from discovery to present day.Nature reviews. Immunology · 2023
    Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Negative Regulation of Cytosolic Sensing of DNA.International review of cell and molecular biology · 2019
    Review
  17. Article
  18. 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

8 authors at 1 institution in 1 country.

Aaron M TockerDepartment of Biology, Franklin and Marshall College, Lancaster, PA 17604.ORCID 0000-0002-9672-0357
Emily DurocherDepartment of Biology, Franklin and Marshall College, Lancaster, PA 17604.ORCID 0000-0001-9777-1781
Kimberly D JacobDepartment of Biology, Franklin and Marshall College, Lancaster, PA 17604.
Kate E TrieschmanDepartment of Biology, Franklin and Marshall College, Lancaster, PA 17604.
Suzanna M TalentoDepartment of Biology, Franklin and Marshall College, Lancaster, PA 17604.ORCID 0000-0001-7158-7935
Alma A RechnitzerDepartment of Biology, Franklin and Marshall College, Lancaster, PA 17604.
David M RobertsDepartment of Biology, Franklin and Marshall College, Lancaster, PA 17604.
Beckley K DavisDepartment of Biology, Franklin and Marshall College, Lancaster, PA 17604 beckley.davis@fandm.edu.ORCID 0000-0003-0673-8017
Franklin & Marshall College · US

Funding

Nucleotide binding characteristics of disease associated mutant NOD2 proteinsR15DK098754 · NIDDK · FRANKLIN AND MARSHALL COLLEGE · PI DAVIS, BECKLEY K · 2014 to 2014
$246k
Howard Hughes Medical InstituteNIDDK NIH HHS R15 DK098754
6 · The paper itself

Abstract

Sensing of cytosolic nucleotides is a critical initial step in the elaboration of type I IFN. One of several upstream receptors, cyclic GMP-AMP synthase, binds to cytosolic DNA and generates dicyclic nucleotides that act as secondary messengers. These secondary messengers bind directly to stimulator of IFN genes (STING). STING recruits TNFR-associated NF-κB kinase-binding kinase 1 which acts as a critical node that allows for efficient activation of IFN regulatory factors to drive the antiviral transcriptome. NLRC3 is a recently characterized nucleotide-binding domain, leucine-rich repeat containing protein (NLR) that negatively regulates the type I IFN pathway by inhibiting subcellular redistribution and effective signaling of STING, thus blunting the transcription of type I IFNs. NLRC3 is predominantly expressed in lymphoid and myeloid cells. IQGAP1 was identified as a putative interacting partner of NLRC3 through yeast two-hybrid screening. In this article, we show that IQGAP1 associates with NLRC3 and can disrupt the NLRC3-STING interaction in the cytosol of human epithelial cells. Furthermore, knockdown of IQGAP1 in THP1 and HeLa cells causes significantly more IFN-β production in response to cytosolic nucleic acids. This result phenocopies NLRC3-deficient macrophages and fibroblasts and short hairpin RNA knockdown of NLRC3 in THP1 cells. Our findings suggest that IQGAP1 is a novel regulator of type I IFN production, possibly via interacting with NLRC3 in human monocytic and epithelial cells.

Indexed as

Epithelial CellsHEK293 CellsHeLa CellsHumansImmunityIntercellular Signaling Peptides and ProteinsInterferon Type IMacrophagesMembrane ProteinsNucleic AcidsProtein Bindingras GTPase-Activating ProteinsRNA, Small InterferingSignal TransductionSTING ProteinVirus DiseasesIntercellular Signaling Peptides and ProteinsInterferon Type IIQ motif containing GTPase activating protein 1Membrane ProteinsNLRC3 protein, humanNucleic Acidsras GTPase-Activating ProteinsRNA, Small InterferingSTING1 protein, humanSTING Protein

Identifiers

PMID28864474
PMCPMC5714304
OpenAlexW2751837488

What OpenQuestion holds

Textmetadata
LicenceTDM
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.