Evidence map›Paper›PMID 2247055›Full record

ArticleMolecular and cellular biology1990

A 58-base-pair region of the human C3 gene confers synergistic inducibility by interleukin-1 and interleukin-6.

D R Wilson, T S Juan, M D Wilde, G H Fey, G J Darlington

Open access · greenAbstract readComparative Study
In one paragraph

Article in Molecular and cellular biology, 1990. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.8field-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

34 citing papers in PubMed, 90 citations in OpenAlex.

  1. Review
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  9. Candidate genes for temporal lobe epilepsy: a replication study.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2008
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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 1 institution in 1 country.

D R WilsonDepartment of Pathology, Baylor College of Medicine, Houston, Texas 77030.
T S Juan
M D Wilde
G H Fey
G J Darlington
Baylor College of Medicine · US

Funding

SENESCENT CELL PROLIFERATION AND GENE EXPRESSIONP01AG007123 · NIA · BAYLOR COLLEGE OF MEDICINE · PI SMITH, JAMES · 1987 to 1995
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STRUCTURE AND REGULATION OF LIVER ACUTE PHASE GENESR01AI022166 · NIAID · SCRIPPS RESEARCH INSTITUTE · PI COOPER, NEIL R. · 1985 to 1993
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ACTIVATION OF HUMAN HEPATIC GENES IN CELL HYBRIDSR01GM032111 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI DARLINGTON, GRETCHEN J. · 1985 to 1991
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NIAID NIH HHS AI22166NIA NIH HHS AG07123NIGMS NIH HHS GM 32111
6 · The paper itself

Abstract

We have cloned the promoter for the human third component of complement (C3) gene and have identified sequences involved in its regulation during the acute-phase response. A construct linking 199 bp of the C3 promoter to the firefly luciferase gene was found to be very responsive to interleukin-1 (IL-1) and modestly responsive to interleukin-6 (IL-6) by transfection analysis in the human hepatoma line Hep3B2. Simultaneous treatment with the two cytokines showed a strong synergy between the actions of the two molecules. A 58-bp fragment (-127 to -70 bp) was shown by 5' and 3' deletional mutagenesis to contain cis-acting elements that mediated both the IL-1 response and the IL-1-plus-IL-6 synergistic response of this promoter. When coupled to a heterologous promoter, this fragment enabled the synergistic induction by IL-1 plus IL-6. Sequences homologous to the palindrome ACATTGCACAATCT, which mediates the induction of the IL-6 gene by IL-1 (S. Akira, H. Isshiki, T. Sugita, O. Tanabe, S. Kinoshita, Y. Nishio, T. Nakajima, T. Hirano, and T. Kishimoto, EMBO J. 9:1897-1906, 1990), and the core sequence of the IL-6-responsive element of the rat alpha 2-macroglobulin gene (CTGGGA; M. Hattori, L. J. Abraham, W. Northemann, and G. H. Fey, Proc. Natl. Acad. Sci. USA 87:2364-2368, 1990) are contained within this fragment in immediate juxtaposition and partially overlapping. Site-directed mutagenesis within this homology region drastically reduced the inducibility of the C3 promoter by either cytokine. DNase I footprinting analysis defined a binding site for the transcription factor CCAAT/enhancer-binding protein (C/EBP), which included the IL-1-responsive element-like sequence. No differences were seen between the footprints generated by using extracts from unstimulated and IL-1-stimulated Hep3B2 cells. However, gel retardation analyses revealed two IL-1-specific bands. The data suggest that the induction by IL-1 is mediated by a factor belonging to the family of C/EBP-related proteins.

Indexed as

AnimalsBase CompositionBase SequenceCloning, MolecularColeopteraComplement C3Deoxyribonuclease IDrug SynergismHumansInterleukin-1Interleukin-6LuciferasesMiceMolecular Sequence DataMolecular WeightMutagenesis, Site-DirectedComplement C3Deoxyribonuclease IInterleukin-1Interleukin-6LuciferasesOligonucleotide ProbesRecombinant Proteins

Identifiers

PMID2247055
PMCPMC362893
OpenAlexW1871178731

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.