Evidence map›Paper›PMID 11175347›Full record

ArticleOncogene2000

NO activation of fos promoter elements requires nuclear translocation of G-kinase I and CREB phosphorylation but is independent of MAP kinase activation.

T Gudi, D E Casteel, C Vinson, G R Boss, R B Pilz

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 94 citations in OpenAlex.

  1. Review
  2. Review
  3. Myokine Musclin Is Critical for Exercise-Induced Cardiac Conditioning.International journal of molecular sciences · 2023
    Article
  4. The Interplay between cGMP and Calcium Signaling in Alzheimer's Disease.International journal of molecular sciences · 2022
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Synaptic therapy in Alzheimer's disease: a CREB-centric approach.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2015
    Review
  12. Article
  13. Inositol polyphosphate multikinase is a coactivator for serum response factor-dependent induction of immediate early genes.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  14. Proprotein convertases play an important role in regulating PKGI endoproteolytic cleavage and nuclear transport.American journal of physiology. Lung cellular and molecular physiology · 2013
    Article
  15. Review
  16. Article
  17. Article
  18. Nuclear entry of a cGMP-dependent kinase converts transient into long-lasting olfactory adaptation.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  19. Article
  20. 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

5 authors at 2 institutions in 1 country.

T GudiDepartment of Medicine and Cancer Center, University of California, San Diego, La Jolla, California, CA 92093-0652, USA.
D E Casteel
C Vinson
G R Boss
R B Pilz
University of California, San Diego · USNational Institutes of Health · US

Funding

HEMOGLOBIN AND BLOOD PROTEIN CHEMISTRYT32DK007233 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KOMIVES, ELIZABETH A. · 1986 to 2012
$4.6M
REGULATION OF GENE EXPRESSION BY NO/CGMPR01GM055586 · NIGMS · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI PILZ, RENATE B · 1998 to 2002
$707k
NIDDK NIH HHS 5T32DK07233-24NIGMS NIH HHS R01GM055586
6 · The paper itself

Abstract

We have shown that nitric oxide (NO) regulates c-fos gene expression via cGMP-dependent protein kinase (G-kinase), but NO's precise mechanism of action is unclear. We now demonstrate that: (1) NO targets two transcriptional elements in the fos promoter, i.e., the fos AP-1 binding site and the cAMP-response element (CRE); (2) NO activation of these two enhancer elements requires the CRE binding protein CREB because a dominant negative CREB fully inhibits NO transactivation of reporter genes whereas dominant negative Fos or CCAAT enhancer binding proteins have no effect; (3) CREB is phosphorylated by G-kinase in vitro and its phosphorylation increases in vivo when G-kinase is activated either directly by cGMP or indirectly by NO via soluble guanylate cyclase; (4) NO activation of fos promoter elements requires nuclear translocation of G-kinase but not activation of mitogen-activated protein kinases.

Indexed as

Genes, fosMAP Kinase Signaling SystemActive Transport, Cell NucleusAnimalsCell LineCell NucleusCricetinaeCyclic AMP Response Element-Binding ProteinCyclic GMP-Dependent Protein KinasesEnhancer Elements, GeneticGenes, ReporterGuanylate CyclaseMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Mitogen-Activated Protein KinasesMutationCyclic AMP Response Element-Binding ProteinCyclic GMP-Dependent Protein KinasesGuanylate CyclaseMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Mitogen-Activated Protein KinasesNitric Oxidep38 Mitogen-Activated Protein Kinases

Identifiers

PMID11175347
OpenAlexW1979057802

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.