Evidence map›Paper›PMID 8196668›Full record

ArticleMolecular and cellular biology1994

Serum amyloid A gene expression under acute-phase conditions involves participation of inducible C/EBP-beta and C/EBP-delta and their activation by phosphorylation.

A Ray, B K Ray

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 118 citations in OpenAlex.

  1. Review
  2. Kidney Involvement in Autoinflammatory Diseases.Kidney diseases (Basel, Switzerland) · 2023
    Review
  3. Article
  4. Hepatocytes: a key cell type for innate immunity.Cellular & molecular immunology · 2016
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. The many faces of C/EBPδ and their relevance for inflammation and cancer.International journal of biological sciences · 2013
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Orthogonal analysis of C/EBPbeta targets in vivo during liver proliferation.Proceedings of the National Academy of Sciences of the United States of America · 2004
    Article
  19. Article
  20. Review
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.

A RayDepartment of Veterinary Microbiology, University of Missouri, Columbia 65211.
B K Ray
Missouri College · US

Funding

REGULATION OF SERUM AMYLOID A PROTEIN SYNTHESISR15DK045144 · NIDDK · UNIVERSITY OF MISSOURI-COLUMBIA · PI RAY, BIMAL K · 1992 to 1992
–
NIDDK NIH HHS DK 45144-01
6 · The paper itself

Abstract

Serum amyloid A (SAA) is a plasma protein whose synthesis is markedly increased in the liver during the inflammatory process. Previous analysis of SAA promoter function implicated the involvement of the CCAAT/enhancer-binding protein (C/EBP) in controlling this process. In this study, using antibodies against three C/EBP isoforms in DNA-binding and Western blot (immunoblot) assays, we found that in response to inflammatory signals, both C/EBP-delta and C/EBP-beta are induced and that their interactions with the SAA promoter element are necessary for the increased SAA gene expression. Cotransfections of liver cells with an SAA promoter-linked reporter chloramphenicol acetyltransferase gene and murine sarcoma virus-expressed C/EBP-delta or C/EBP-beta confirm such phenomena. The increased transactivating ability in the presence of the cellular phosphatase inhibitors okadaic acid and sodium orthovanadate, coupled with the observation that dephosphorylation severely inhibits the DNA-binding ability in vitro, implicates a role of phosphorylation in the regulation of the activities of the C/EBP-delta isoform. Consistent with these findings, we have detected higher levels of DNA-binding activity of C/EBP-delta prepared from cells treated with phosphatase inhibitors. We also present evidence that C/EBP-delta is a phosphoprotein. These results suggest that C/EBP-delta is regulated by phosphorylation and, in conjunction with C/EBP-beta, is one of the major proteins responsible for the increased transcription of the SAA gene in response to inflammatory stimuli.

Indexed as

Gene ExpressionAnimalsBase SequenceCCAAT-Enhancer-Binding ProteinsCell LineCell NucleusDNA-Binding ProteinsKineticsLiverMaleMolecular Sequence DataMutagenesisNuclear ProteinsOligodeoxyribonucleotidesPhosphorylationRabbitsCCAAT-Enhancer-Binding ProteinsDNA-Binding ProteinsNuclear ProteinsOligodeoxyribonucleotidesSerum Amyloid A ProteinTranscription Factors

Identifiers

PMID8196668
PMCPMC358798
OpenAlexW2110146202

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.